3-phenylsulphonyl-quinoline derivatives as agents for treating pathogenic blood vessels disorders

Abstract

The disclosure provides compounds, and compositions, including pharmaceutical compositions, kits that include the compounds, and methods of using (or administering) and making the compounds. The disclosure further provides compounds or compositions thereof for use in a method of modulating PLXDC1 (TEM7) and / or PLXDC2 or killing pathogenic blood vessles. The disclosure further provides compounds or compositions thereof for use in a method of treating a disease, disorder, or condition that is mediated, at least in part, by PEDF receptors or by angiogenesis.

Description

CROSS REFERENCE TO RELATED APPLICATIONS

[0001] This application claims priority to U.S. Provisional Application No. 62 / 916,983 filed on October 18, 2019, which is incorporated herein by reference in its entirety. FIELD

[0002] The present disclosure relates generally to small molecules that target pathogenic blood vessels, compositions comprising the same, and methods of using the compounds and compositions for treating cancer and other pathogenic blood vessel disorders. BACKGROUND

[0003] Angiogenesis plays a key role in the pathogenesis of several major human diseases. In addition to tumor growth and metastasis, angiogenesis is a major driving force in several blinding diseases including diabetic retinopathy, age-related macular degeneration (AMD), and retinopathy of prematurity. AMD and diabetic retinopathy are the leading causes of blindness in the elderly and populations at the working age in the United States, respectively. Retinopathy of prematurity is a common reason that causes the loss of vision for newborn babies.

[0004] Angiogenesis also plays a role in pathogenesis of cancer, e.g., tumor development, since newly-formed blood vessels supply the tumor with growth nutrients and signals that allow the tumor to grow and spread. Accordingly, cutting off a tumor’s supply of nutrients and primary mechanism for traveling to distant sites is an attractive therapeutic strategy. However, current anti-angiogenic strategies only target newly formed blood vessels, and are unable to target existing blood vessels that contribute to disease progression.

[0005] Different disease progression patterns can be induced by anti-angiogenic therapies, which may lead to worse outcomes in terms of drug resistance, invasion, and metastasis. Furthermore, targeting angiogenesis does not treat existing blood vessels that may have, for example, already vascularized a tumor. There is a need in the art for complementary therapies that, in contrast to anti-angiogenic therapies, can target existing blood vessels and treat cancer and other disorders arising from angiogenesis (collectively referred to herein as pathogenic blood vessel disorders). SUMMARY

[0006] The disclosure provides compounds, and compositions, including pharmaceutical compositions, kits that include the compounds, and methods of using (or administering) and making the compounds. The disclosure further provides compounds or compositions thereof for use in a method of modulating PLXDC1 (TEM7) and / or PLXDC2 or killing pathogenic blood vessles. The disclosure further provides compounds or compositions thereof for use in a method of treating a disease, disorder, or condition that is mediated, at least in part, by PEDF receptors or by angiogenesis.

[0007] In certain embodiments, provided are compounds of Formula (I) or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein Formula (I) is R8                                  (I), wherein each of n, R1, R2, R5, R6, R7, R8 and R9 is as defined herein.

[0008] In certain embodiments, provided is a pharmaceutical composition comprising a compound as described herein, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, and a pharmaceutically acceptable carrier.

[0009] In some embodiments, the compound activates the PLXDC (e.g., PLXDC1 and / or PLXDC2) protein. In some embodiments, the compound induces NFkB activation. In some embodiments, the compound induces NFkB activation in pathogenic blood vessels. In some embodiments, the compound increases necrosis of pathogenic blood vessels. In some embodiments, the pathogenic blood vessel-related disorder comprises diabetic retinopathy, age-related macular degeneration (AMD), retinopathy of prematurity, or cancer. In some embodiments, the pathogenic blood vessel-related disorder comprises cancer. In some embodiments, the cancer comprises colon cancer. In some embodiments, the cancer comprises lung cancer. In some embodiments, the cancer comprises a solid tumor. In some embodiments, the cancer comprises a vascularized tumor.

[0010] In some embodiments, the pathogenic blood vessel-related disorder comprises cancer and further wherein the patient is one that has a malignant tumor. In some embodiments, the tumor comprises a solid tumor. In some embodiments, the tumor has a diameter of greater than 2 cm. In some embodiments, the tumor has a diameter of at least, or at most 1, 2, 3, 4, 5, 6, 7, or 8 cm (or any range derivable therein).

[0011] In some embodiments, the compound specifically induces endothelial cell necrosis in the targeted blood vessels. In some embodiments, the compound does not directly induce tumor cell necrosis. In some embodiments, the compound induces and / or increases coagulative necrosis in a tumor in the patient. In some embodiments, the compound induces and / or increases infarction in the tumor. In some embodiments, the patient has been determined to have pathogenic blood vessels. In some embodiments, the patient has been determined to have PLXDC1 and / or PLXDC 1-expressing cells. In some embodiments, the expressing cells comprise endothelial cells. In some embodiments, the expressing cells comprise cell surface expression of PLXDC1 and / or PLXDC2.

[0012] In some embodiments, the patient has previously been treated for the pathogenic blood vessel-related disorder with an additional therapy. In some embodiments, the patient has been determined to be non-responsive or have a toxic response to the additional therapy. In some embodiments, the additional therapy comprises an anti-angiogenic therapy. In some embodiments, the additional therapy comprises an immunotherapy. In some embodiments, the patient has not previously been treated for the pathogenic blood vessel-related disorder.

[0013] In certain embodiments, provided is a method for treating a disease or disorder that is mediated, at least in part, by PLXDC1 and / or PLXDC2 in a subject in need thereof, the method comprising administering to the subject an effective amount of a compound or a pharmaceutical composition comprising a compound as described herein, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof.

[0014] The disclosure also provides uses of the compounds, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, in the manufacture of a medicament for modulating PLXDC (e.g., PLXDC1 and / or PLXDC2). Moreover, the disclosure provides uses of the compounds, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, in the manufacture of a medicament for the treatment of a disease, disorder, or condition that is mediated, at least in part, by PLXDC 1 and / or PLXDC2.

[0015] The disclosure also provides use of the compounds, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, in treating a disease, such as cancer, retinal occlusive vascular disease, retinopathy of prematurity, diabetic retinopathy, and age-related macular degeneration.

[0016] These and other aspects of the disclosure is further described in the texts that follow. BRIEF DESCRIPTION OF THE DRAWINGS

[0017] The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present invention. The invention may be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.

[0018] FIG. 1A-H. Expression of PLXDC 1 in pathogenic blood vessels in choroidal neovascularization (CNV) and ischemia-induced retinopathy. Red channel shows blood vessel marker Griffonia Simplicifolia Lectin I-isolectin B4. Green channel shows anti-PLXDCl signal. A-D. Highly enriched PLXDC 1 expression in pathogenic blood vessels in a mouse model of CNV (laser-induced -3 - CNV). A&B, retina sections. Arrowheads indicate examples of normal inner retinal blood vessels (in A) that are negative for PLXDC1 signal (in B). C&D, staining done on flat-mounted eye cup. E-H. High expression of PLXDC1 in pathogenic blood vessels in a mouse model of ischemia-induced retinopathy, but not in blood vessels of healthy retina. E&F. P17 retina of ischemia-induced retinopathy (E and F are the same section stained by endothelial cell marker and PLXDC1 antibody, respectively). Examples of pathogenic blood vessels expressing PLXDC1 are indicated by white arrows. G&H. P17 healthy retina (G and H are the same section stained by endothelial cell marker and PLXDC1 antibody, respectively). Examples of healthy blood vessels showing no detectable PLXDC1 expression are indicated by white arrows in G (there is no corresponding PLXDC1 signals in H). CH, choroid. ON, outer nuclear layer. IN, inner nuclear layer. GC, ganglion cell layer.

[0019] FIG. 2A-E. Comparison of compound 369 with the current anti-angiogenic drug in an ex vivo model of choroidal angiogenesis. A. A schematic diagram of the timeframe of the experiment. Treatment does not start until choroidal angiogenesis occurs for 7 days. Treatment lasts for two days before cell death and survival are analyzed. B. Control experiment without any drug treatment at day 7. The white circle in the middle delineates the piece of choroid / RPE that was embedded to initiate neovascularization. C. The most commonly used drug for choroidal neovascularization, Eylea, can inhibit choroidal endothelial cell growth (as expected of an antiangiogenesis drug). Eylea was added at 10 pM. D. Compound 369 that targets PLXDC1 / PLXDC2 can kill the new endothelial cells in choroidal angiogenesis. Choroid and RPE are still alive after the treatment, demonstrating the high specificity of the treatment. The compound was added at 10 pM. In B-D, green cells are live cells and red cells are dead cells. E. Quantitation of the experiments described in B-D. The amount of new endothelial cells in the untreated control is defined as 100%.

[0020] FIG. 3A-B shows tumor shrinkage and necrosis following treatment with certain compounds described herein. FIG. 3A shows that 3 days after injection, all the tumors were shrinking. FIG. 3B shows that the tumor shrinkage was maintained 6 days after injection.

[0021] FIG. 4A-B show tumor shrinkage and necrosis following treatment with compounds described herein. FIG. 4A shows that 3 days after injection, all the tumors were shrinking. FIG. 4B shows that the tumor shrinkage was maintained 6 days after injection.

[0022] FIG. 5A-B show activation of PLXDC1 and PLXDC2 by small molecules. Through RNAseq analysis of PLXDC1-expressing endothelial cells killing by PLXDC1-activating compounds, a transcriptional factor called Gfilb was found to be induced during PLXDC1-mediated cell killing. By linking its promotor to a luciferase reporter gene, this example developed a PLXDC1 receptor activation assay that demonstrates the activation of the receptor by its ligands. A. PLXDC1-activating compounds (A-Com-1 and A-Com-2) highly activated the promotor activity in PLXDCl-expressing cells. B. A-Com-1 and A-Com-2 also activated the promotor activity in PLXDC2-expressing cells. However, both compounds preferentially activate PLXDC1 over PLXDC2. A-Com-2 more strongly differentiates between the two receptors. All compound treatments were done for 1 day. Basal promotor activity of the PLXDC1-expressing cells is defined as 1. Fluorouracil (FU), a chemotherapy drug that kills dividing cells by apoptosis, do not activate this promotor.

[0023] FIG. 6A-B show killing of PLXDC1-expressing endothelial cells by PLXDC1-activating small molecules and antibodies. A. Visualization of the killing human PLXDC1-expressing endothelial cells by PLXDC1-activating small molecule (compound). The top three pictures on represent control cells and the lower three pictures represent compound-treated cells, showing light microscopy picture (left), live cell (middle) and dead cell staining (right). Live cells are stained using Fluorescein diacetate (green signal) and dead cells are stained using propidium iodide (red signal). B. Quantitation of the killing of human PLXDC1-expressing endothelial cells by PLXDC1-activating small molecules (A-Compound-1 and A-Compound-2) and antibodies (A-TEM7-Ab-1 and A-TEM7-Ab-2). Incubation time of the compounds and antibodies is 24 hours. Cell survival of the control cells is defined as 100%.

[0024] FIG. 7A-D show that PLXDC1-activating compound specifically suppresses pathogenic blood vessels in vivo without affecting healthy blood vessels in ischemia-induced retinopathy. A. Upper graph: Schematic diagram of the experimental design for ischemia-induced retinopathy. The high oxygen environment caused blood vessel loss (vaso-obliteration). In room air, loss of vessels triggered abnormal angiogenesis that generated pathogenic blood vessels on the top of the retina (marked in yellow in D). Treatment was applied during the return to room air by subcutaneous injection. Lower graph: quantitation of healthy blood vessels, vaso-obliteration and pathogenic blood vessels between the control (n=10) and treated retinas (n=10). Treatment by PLXDC1-activating compound (A-Compound-1) highly suppressed pathogenic blood vessels (two asterisks) while improving the amount of healthy blood vessels (one asterisk). B. Representative images of flatmounted control retinas (upper two images) and retinas from compound treated mice (lower two images). Red signal is blood vessel marker. C. The same retinas in B with vaso-obliteration areas marked in white color. These images illustrate that compound-treated retinas went through vaso-obliteration like the control retinas. D. The same retinas in B with pathogenic blood vessels marked in yellow color. These images illustrate that compound-treated retinas have highly decreased pathogenic blood vessels as compared to the control retinas.

[0025] FIG. 8A-C show that PLXDC1-activating compound causes tumor shrinkage in vivo. Treatment was done at day 0 by bolus IV injection. A. Raw data of tumor growth curves of the mice in the control group. B. Raw data of tumor growth curves of the mice in the treatment group. C. Comparison of the combined growth data of the control group and the treatment group.

[0026] FIG. 9 shows tumor morphological changes on live animals due to the treatment by PLXDC1-activating compound. Pictures of the whole animals in the experiment described in Figure 11 show tumor morphological and color changes on day 1 and day 3. Treatment was done at day 0. Tumors in the treatment groups becomes darker in color on day 1 due to the destruction of tumor blood vessels and accumulation of blood in the tumors. Tumors in the treatment groups start to become yellower in color on day 3, consistent with the onset of tumor necrosis due to the lack of tumor blood vessels.

[0027] FIG. 10A-B show tumor morphological changes on live animals due to the treatment by PLXDC1-activating compound. Treatment was done at day 0. While the tumors in the control group have grown to large sizes, tumors in the treatment groups have highly shrunk in size and become yellow in color.

[0028] FIG. 11A-B show morphological changes of dissected tumors due to the treatment by PLXDC1-activating compound. Pictures of the dissected tumors in the experiment described in Figure 11 show tumor morphological and color changes on day 7. While the tumors in the control group are reddish in color, tumors in the treatment groups have highly shrunk in size and become yellow in color, consistent with the lack of tumor blood vessels and tumor necrosis. DETAILED DESCRIPTION

[0029] The following description sets forth exemplary embodiments of the present technology. It should be recognized, however, that such description is not intended as a limitation on the scope of the present disclosure but is instead provided as a description of exemplary embodiments. 1. Definitions

[0030] As used in the present specification, the following words, phrases and symbols are generally intended to have the meanings as set forth below, except to the extent that the context in which they are used indicates otherwise.

[0031] A dash that is not between two letters or symbols is used to indicate a point of attachment for a substituent. For example, -C(O)NH2 is attached through the carbon atom. A dash at the front or end of a chemical group is a matter of convenience; chemical groups may be depicted with or without one or more dashes without losing their ordinary meaning. A wavy line or a dashed line drawn through a line in a structure indicates a specified point of attachment of a group. Unless chemically or structurally required, no directionality or stereochemistry is indicated or implied by the order in which a chemical group is written or named.

[0032] The prefix “Cu v” indicates that the following group has from u to v carbon atoms. For example, “Ci-6 alkyl” indicates that the alkyl group has from 1 to 6 carbon atoms.

[0033] Reference to “about” a value or parameter herein includes (and describes) embodiments that are directed to that value or parameter per se. In certain embodiments, the term “about” includes the indicated amount ± 10%. In other embodiments, the term “about” includes the indicated amount ± 5%. In certain other embodiments, the term “about” includes the indicated amount ± 1%. Also, to the term “about X” includes description of “X”. Also, the singular forms “a” and “the” include plural references unless the context clearly dictates otherwise. Thus, e.g., reference to “the compound” includes a plurality of such compounds and reference to “the assay” includes reference to one or more assays and equivalents thereof known to those skilled in the art.

[0034] “Alkyl” refers to an unbranched or branched saturated hydrocarbon chain. In some embodiments, alkyl has the indicated number of carbon atoms. In some embodiments, alkyl has 1 to 40 carbon atoms (i.e., Cuo alkyl), 1 to 30 carbon atoms (i.e., C1-30 alkyl), 10 to 30 carbon atoms (i.e., C10 30 alkyl), 1 to 20 carbon atoms (i.e., C1-20 alkyl), 1 to 12 carbon atoms (i.e., C112 alkyl), 1 to 8 carbon atoms (i.e., Ci s alkyl), 1 to 6 carbon atoms (i.e., C1-6 alkyl) or 1 to 4 carbon atoms (i.e., C1-4 alkyl). Examples of alkyl groups include, e.g., methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl, 2-pentyl, isopentyl, neopentyl, hexyl, 2-hexyl, 3-hexyl and 3-methylpentyl, octyl, nonyl, decyl, dodecyl, icosyl, docosyl, tetradecyl.. When an alkyl residue having a specific number of carbons is named by chemical name or identified by molecular formula, all positional isomers having that number of carbons may be encompassed; thus, for example, “butyl” includes n-butyl (i.e., -(CFE^CFE), sec-butyl (i.e., -CH(CH3)CH2CH3), isobutyl (i.e., -CH2CH(CH3)2) and tertbutyl (i.e., -C(CH3)3); and “propyl” includes n-propyl (i.e., -(CH2)2CH3) and isopropyl (i.e., -CH(CH3)2).

[0035] Certain commonly used alternative chemical names may be used. For example, a divalent group such as a divalent “alkyl” group, a divalent “aryl” group, etc., may also be referred to as an “alkylene” group, an “arylene” group, respectively. Also, unless indicated explicitly otherwise, where combinations of groups are referred to herein as one moiety, e.g., arylalkyl or aralkyl, the last mentioned group contains the atom by which the moiety is attached to the rest of the molecule.

[0036] “Alkenyl” refers to an alkyl group containing at least one carbon-carbon double bond. In some embodiments, alkenyl has the indicated number of carbon atoms. In some embodiments, alkenyl has from 2 to 40 carbon atoms (i.e., C240 alkenyl), 2 to 30 carbon atoms (i.e., C2 30 alkenyl), 10 to 30 carbon atoms (i.e., C10 30 alkenyl), 2 to 20 carbon atoms (i.e., C2 20 alkenyl), 2 to 8 carbon atoms (i.e., C2 s alkenyl), 2 to 6 carbon atoms (i.e., C2 6 alkenyl) or 2 to 4 carbon atoms (i.e., C24 alkenyl). Examples of alkenyl groups include, e.g., ethenyl, propenyl, butadienyl (including 1,2-butadienyl and 1,3-butadienyl).

[0037] “Alkynyl” refers to an alkyl group containing at least one carbon-carbon triple bond. In some embodiments, alkynyl has the indicated number of carbon atoms. In some embodiments, alkynyl has from 2 to 40 carbon atoms (i.e., C2-40 alkynyl), 2 to 30 carbon atoms (i.e., C1-30 alkynyl), 10 to 30 carbon atoms (i.e., C10 30 alkynyl), 2 to 20 carbon atoms (i.e., C2 20 alkynyl), 2 to 8 carbon atoms (i.e., C2 s alkynyl), 2 to 6 carbon atoms (i.e., C2-6 alkynyl) or 2 to 4 carbon atoms (i.e., C2 4 alkynyl). The term “alkynyl” also includes those groups having one triple bond and one double bond.

[0038] “Alkoxy” refers to the group “alkyl-O-”. In some embodiments, alkoxy has from 1 to 40 carbon atoms (i.e., -O-C1-40 alkyl), 1 to 30 carbon atoms (i.e., -O-Ci 30 alkyl), 10 to 30 carbon atoms (i.e., -O-C10 30 alkyl, 1 to 20 carbon atoms (i.e., -O-Ci 20 alkyl), 1 to 12 carbon atoms (i.e., -O-C1-12 alkyl), 1 to 8 carbon atoms (i.e., -O-Ci 8 alkyl), 1 to 6 carbon atoms (i.e., -O-Ci 6 alkyl) or 1 to 4 carbon atoms (i.e., -O-Ci 4 alkyl). Examples of alkoxy groups include, e.g., methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, tert-butoxy, sec-butoxy, n-pentoxy, n-hexoxy and 1,2-dimethylbutoxy.

[0039] “Alkenoxy” refers to the group “alkene-O-”. In some embodiments, alkenoxy has from 2 to 40 carbon atoms (i.e., -O-C240 alkene), 2 to 30 carbon atoms (i.e., -O-C230 alkene), 10 to 30 carbon atoms (i.e., -O-C10 30 alkene), 2 to 20 carbon atoms (i.e., -O-C2 20 alkene), 2 to 12 carbon atoms (i.e., -O-C212 alkene), 2 to 8 carbon atoms (i.e., -O-C2 8 alkene), 2 to 6 carbon atoms (i.e., -O-C2 6 alkene) or 2 to 4 carbon atoms (i.e., -O-C2 4 alkene).

[0040] “Alkynoxy” refers to the group “alk2ne-O-”. In some embodiments, alkynoxy has from 1 to 40 carbon atoms (i.e., -O-C240 alkyne), 2 to 30 carbon atoms (i.e., -O-C2 30 alkene), 10 to 30 carbon atoms (i.e., -O-C10 30 alkyne, 2 to 20 carbon atoms (i.e., -O-C2 20 alkyne), 2 to 12 carbon atoms (i.e., -O-C212 alkyne), 2 to 8 carbon atoms (i.e., -O-C2 8 alkyne), 2 to 6 carbon atoms (i.e., -O-C2 6 alkyne) or 2 to 4 carbon atoms (i.e., -O-C2 4 alkyne).

[0041] The term “amido” as used herein refers to both -NR8C(=O)Rh and -C(=O)NR8Rh, wherein each of R8 and Rh is independently hydrogen, alkyl, alkenyl, alkynyl, alkoxy, thioalkyl, aryl, arylalkyl, cycloalkyl, cycloalkyl-alkyl, haloalkyl, heterocyclyl, heterocyclyl-alkyl, heteroaryl, or heteroaryl-alkyl, and further wherein each R8 and Rh may be optionally substituted, as defined herein.

[0042] “Amino” refers to the group -NRyRz wherein Ry and Rz are independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroalkyl or heteroaryl; each of which may be optionally substituted, as defined herein.

[0043] “Aryl” refers to an aromatic carbocyclic group having a single ring (e.g., monocyclic) or multiple rings (e.g., bicyclic or tricyclic) including fused systems. In some embodiments, aryl has 6 to 20 ring carbon atoms (i.e., Ce 20 aryl), 6 to 12 ring carbon atoms (i.e., Ce 12 aryl), or 6 to 10 ring carbon atoms (i.e., Ce 10 aryl). Examples of aryl groups include, e.g., phenyl, naphthyl, fluorenyl and anthryl. Aryl, however, does not encompass or overlap in any way with heteroaryl defined below. If one or more aryl groups are fused with a heteroaryl, the resulting ring system is heteroaryl. If one or more aryl groups are fused with a heterocyclyl, the resulting ring system is heterocyclyl.

[0044] “Arylalkyl” or “Aralkyl” refers to the group “aryl-alkyl-”.

[0045] “Carboxyl ester” or “ester” refer to both -OC(O)RX and -C(O)ORX, wherein Rx is alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroalkyl or heteroaryl; each of which may be optionally substituted, as defined herein.

[0046] “Carboxy” as used herein refers to -CO2H, or a salt thereof. Exemplary counter ions which can be used include, but are not limited to, Na+, K+, Li+, NHZ and others described herein.

[0047] “Cycloalkyl” refers to a saturated or partially unsaturated cyclic alkyl group having a single ring or multiple rings including fused, bridged and spiro ring systems. The term “cycloalkyl” includes cycloalkenyl groups (i.e., the cyclic group having at least one double bond) and carbocyclic fused ring systems having at least one sp3 carbon atom (i.e., at least one non-aromatic ring). In some embodiments, cycloalkyl has from 3 to 20 ring carbon atoms (i.e., C3 20 cycloalkyl), 3 to 12 ring carbon atoms (i.e., C312 cycloalkyl), 3 to 10 ring carbon atoms (i.e., C310 cycloalkyl), 3 to 8 ring carbon atoms (i.e., C3-8 cycloalkyl), or 3 to 6 ring carbon atoms (i.e., C3 6 cycloalkyl). Monocyclic groups include, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl. Polycyclic cycloalkyl refers to a cycloalkyl having at least two rings, which may be a fused, bridged or spiro ring system. Polycyclic groups include, for example, bicyclo[2.2.1]heptanyl, bicyclo[2.2.2]octanyl, adamantyl, norbornyl, decalinyl, 7,7-dimethyl-bicyclo[2.2.1]heptanyl and the like. “Spirocycloalkyl” refers to a polycyclic cycloalkyl group wherein at least two rings are linked together by one common atom, for example spiro[2.5]octanyl, spiro[4.5]decanyl, or spiro[5.5]undecanyl. Spirocycloalkyl may contain fused rings in the ring system, but not bridged rings. “Fused cycloalkyl” refers to a polycyclic cycloalkyl group wherein at least two rings are linked together by two common atoms wherein the two common atoms are connected through a covalent bond. Fused cycloalkyl does not contain any spiro or bridged rings in the ring system. “Bridged cycloalkyl” refers to a polycyclic cycloalkyl that contains a bridge—an alkylene (such as Cm alkylene) group that connect two "bridgehead" atoms. Non-limiting examples of bridged cycloalkyl include bicyclo[2.2.1]heptanyl, bicyclo[2.2.2]octanyl, adamantyl, norbornyl, and 7,7-dimethyl-bicyclo[2.2.1]heptanyl. Bridged cycloalkyl may contain fused and / or spiro rings in the ring system. Further, the term cycloalkyl is intended to encompass any non-aromatic ring which may be fused to an aryl ring, regardless of the attachment to the remainder of the molecule.

[0048] “Halogen” or “halo” refers to atoms occupying group VIIA of the periodic table, such as fluoro, chloro, bromo or iodo.

[0049] “Haloalkyl” refers to an unbranched or branched alkyl group as defined above, wherein one or more (e.g., 1 to 6, 1 to 5 or 1 to 3) hydrogen atoms are replaced by a halogen. For example, where a residue is substituted with more than one halogen, it may be referred to by using a prefix corresponding to the number of halogen moieties attached. Dihaloalkyl and trihaloalkyl refer to alkyl substituted with two (“di”) or three (“tri”) halo groups, which may be, but are not necessarily, the same halogen. Examples of haloalkyl include, e.g., trifluoromethyl, difluoromethyl, fluoromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 1,2-difluoroethyl, 3-bromo-2-fluoropropyl, 1,2-dibromoethyl and the like.

[0050] “Haloalkoxy” refers to an alkoxy group as defined above, wherein one or more (e.g., 1 to 6, 1 to 5 or 1 to 3) hydrogen atoms are replaced by a halogen.

[0051] “Hydroxyalkyl” refers to an alkyl group as defined above, wherein one or more (e.g., 1 to 6, 1 to 5 or 1 to 3) hydrogen atoms are replaced by a hydroxy group. A non-limiting example of hydroxyalkyl is -(CH2)i 4-OH.

[0052] “Heteroalkyl” refers to an alkyl group in which one or more, but not all of the carbon atoms (and any associated hydrogen atoms) are each independently replaced with the same or different heteroatomic group, provided the point of attachment to the remainder of the molecule is through a carbon atom. The term “heteroalkyl” includes unbranched or branched saturated chain having carbon and heteroatoms. By way of example, 1, 2 or 3 carbon atoms may be independently replaced with the same or different heteroatomic group. Heteroatomic groups include, but are not limited to, -NRy-, -O-, -S-, -S(O)-, -S(O)2-, and the like, wherein Ryis hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroalkyl or heteroaryl; each of which may be optionally substituted, as defined herein. Examples of heteroalkyl groups include, e.g., ethers (e.g., -CH2OCH3, -CH(CH3)OCH3, -CH2CH2OCH3, -CH2CH2OCH2CH2OCH3, etc.), thioethers (e.g., -CH2SCH3, -CH(CH3)SCH3, -CH2CH2SCH3, -CH2CH2SCH2CH2SCH3, etc.), sulfones (e.g., -CH2S(O)2CH3, -CH(CH3)S(O)2CH3, -CH2CH2S(O)2CH3, -CH2CH2S(O)2CH2CH2OCH3, etc.) and amines (e.g., -CH2NRyCH3, -CH(CH3)NRyCH3, -CH2CH2NRyCH3, -CH2CH2NRyCH2CH2NRyCH3, etc., where Ry is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroalkyl, or heteroaryl; each of which may be optionally substituted, as defined herein). In some embodiments, heteroalkyl includes 1 to 10 carbon atoms (Ci-10 heteroalkyl), 1 to 8 carbon atoms (Ci s heteroalkyl), or 1 to 4 carbon atoms (C1-4 heteroalkyl); and 1 to 3 heteroatoms, 1 to 2 heteroatoms, or 1 heteroatom.

[0053] “Heteroaryl” refers to an aromatic group having a single ring, multiple rings or multiple fused rings, with one or more ring heteroatoms independently selected from nitrogen, oxygen, and sulfur. As used herein, heteroaryl includes 1 to 20 ring carbon atoms (i.e., C1-20 heteroaryl), 3 to 12 ring carbon atoms (i.e., C312 heteroaryl), or 3 to 8 carbon ring atoms (i.e., C3-8 heteroaryl), and 1 to 5 ring heteroatoms, 1 to 4 ring heteroatoms, 1 to 3 ring heteroatoms, 1 to 2 ring heteroatoms, or 1 ring heteroatom independently selected from nitrogen, oxygen and sulfur. In certain instances, heteroaryl includes 5-10 membered ring systems, 5-7 membered ring systems, or 5-6 membered ring systems, each independently having 1 to 4 ring heteroatoms, 1 to 3 ring heteroatoms, 1 to 2 ring heteroatoms, or 1 ring heteroatom independently selected from nitrogen, oxygen and sulfur. Examples of heteroaryl groups include, e.g., acridinyl, benzimidazolyl, benzothiazolyl, benzindolyl, benzofuranyl, benzothiazolyl, benzothiadiazolyl, benzonaphthofuranyl, benzoxazolyl, benzothienyl (benzothiophenyl), benzotriazolyl, benzo[4,6]imidazo[l,2-a]pyridyl, carbazolyl, cinnolinyl, dibenzofuranyl, dibenzothiophenyl, furanyl, isothiazolyl, imidazolyl, indazolyl, indolyl, indazolyl, isoindolyl, isoquinolyl, isoxazolyl, naphthyridinyl, oxadiazolyl, oxazolyl, 1-oxidopyridinyl, 1-oxidopyrimidinyl, 1-oxidopyrazinyl, 1-oxidopyridazinyl, phenazinyl, phthalazinyl, pteridinyl, purinyl, pyrrolyl, pyrazolyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, quinazolinyl, quinoxalinyl, quinolinyl, quinuclidinyl, isoquinolinyl, thiazolyl, thiadiazolyl, triazolyl, tetrazolyl and triazinyl. Examples of the fused-heteroaryl rings include, but are not limited to, benzo[d]thiazolyl, quinolinyl, isoquinolinyl, benzo[b]thiophenyl, indazolyl, benzo[d]imidazolyl, pyrazolo[l,5-a]pyridinyl and imidazo[l,5-a]pyridinyl, where the heteroaryl can be bound via either ring of the fused system. Any aromatic ring, having a single or multiple fused rings, containing at least one heteroatom, is considered a heteroaryl regardless of the attachment to the remainder of the molecule (i.e., through any one of the fused rings). Heteroaryl does not encompass or overlap with aryl as defined above.

[0054] “Heterocyclyl” refers to a saturated or partially unsaturated cyclic alkyl group, with one or more ring heteroatoms independently selected from nitrogen, oxygen and sulfur. The term “heterocyclyl” includes heterocycloalkenyl groups (i.e., the heterocyclyl group having at least one double bond), bridged-heterocyclyl groups, fused-heterocyclyl groups and spiro-heterocyclyl groups. A heterocyclyl may be a single ring or multiple rings wherein the multiple rings may be fused, bridged or spiro, and may comprise one or more (e.g., 1 to 3) oxo (=0) or N-oxide (-0) moieties. Any non-aromatic ring containing at least one heteroatom is considered a heterocyclyl, regardless of the attachment (i.e., can be bound through a carbon atom or a heteroatom). Further, the term heterocyclyl is intended to encompass any non-aromatic ring containing at least one heteroatom, which ring may be fused to an aryl or heteroaryl ring, regardless of the attachment to the remainder of the molecule. As used herein, heterocyclyl has 2 to 20 ring carbon atoms (i.e., C2 20 heterocyclyl), 2 to 12 ring carbon atoms (i.e., C212 heterocyclyl), 2 to 10 ring carbon atoms (i.e., C210 heterocyclyl), 2 to 8 ring carbon atoms (i.e., C2 s heterocyclyl), 3 to 12 ring carbon atoms (i.e., C312 heterocyclyl), 3 to 8 ring carbon atoms (i.e., C3 s heterocyclyl), or 3 to 6 ring carbon atoms (i.e., C3 6 heterocyclyl); having 1 to 5 ring heteroatoms, 1 to 4 ring heteroatoms, 1 to 3 ring heteroatoms, 1 to 2 ring heteroatoms, or 1 ring heteroatom independently selected from nitrogen, sulfur or oxygen. In certain instances, heterocyclyl includes 3- to 10-membered heterocyclyl having 3-10 total ring atoms, 5- to 7-membered heterocyclyl having 5-7 total ring atoms, or 5- or 6-membered heterocyclyl having 5 or 6 total ring atoms. Examples of heterocyclyl groups include, e.g., azetidinyl, azepinyl, benzodioxolyl, benzo[b][l,4]dioxepinyl, 1,4-benzodioxanyl, benzopyranyl, benzodioxinyl, benzopyranonyl, benzofuranonyl, dioxolanyl, dihydropyranyl, hydropyranyl, thienyl[l,3]dithianyl, decahydroisoquinolyl, furanonyl, imidazolinyl, imidazolidinyl, indolinyl, indolizinyl, isoindolinyl, isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl, octahydroisoindolyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, oxazolidinyl, oxiranyl, oxetanyl, phenothiazinyl, phenoxazinyl, piperidinyl, piperazinyl, 4-piperidonyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl, thiazolidinyl, tetrahydrofuryl, tetrahydropyranyl, trithianyl, tetrahydroquinolinyl, thiophenyl (i.e., thienyl), tetrahydropyranyl, thiomorpholinyl, thiamorpholinyl, 1-oxo-thiomorpholinyl and 1,1-dioxo-thiomorpholinyl. The term “heterocyclyl” also includes “spiroheterocyclyl” when there are at least two rings are linked together by one common atom. Examples of the spiroheterocyclyl rings include, e.g., bicyclic and tricyclic ring systems, such as 2-oxa-7-azaspiro[3.5]nonanyl, 2-oxa-6-azaspiro[3.4]octanyl and 6-oxa-l-azaspiro[3.3]heptanyl. Examples of the fused-heterocyclyl rings include, but are not limited to, 1,2,3,4-tetrahydroisoquinolinyl, 4,5,6,7-tetrahydrothieno[2,3-c]pyridinyl, indolinyl and isoindolinyl, where the heterocyclyl can be bound via either ring of the fused system. Examples of heterocyclyl include sugar moieties such as glucose, mannose, allose, altrose, gulose, idose, galactose, and talose.

[0055] The terms “alkylthio” or "thioalkyl" as used herein refer to -S-alkyl, where the term alkyl is as defined herein.

[0056] The term “sulfonamido” as used herein refer to both -NR8S(=O)2Rh and -S(=O)2NR8Rh, wherein each of R8 and Rh is independently hydrogen, alkyl, alkenyl, alkynyl, alkoxy, thioalkyl, aryl, aryl-alkyl, cycloalkyl, cycloalkyl-alkyl, haloalkyl, heterocyclyl, heterocyclyl-alkyl, heteroaryl, or heteroaryl-alkyl, and further wherein each R8 and Rh may be optionally substituted, as defined herein.

[0057] The term “sulfinamido” as used herein refer to both -NR8S(=O)Rh and -S(=O)NR8Rh, wherein each of R8 and Rh is independently hydrogen, alkyl, alkenyl, alkynyl, alkoxy, thioalkyl, aryl, arylalkyl, cycloalkyl, cycloalkyl-alkyl, haloalkyl, heterocyclyl, heterocyclyl-alkyl, heteroaryl, or heteroaryl-alkyl, and further wherein each R8 and Rh may be optionally substituted, as defined herein.

[0058] The term “sulfoxide” or “sulfoxido” refers to the group -S(=O)-R8, wherein R8 is hydrogen, alkyl, alkenyl, alkynyl, alkoxy, thioalkyl, aryl, aryl-alkyl, cycloalkyl, cycloalkyl-alkyl, haloalkyl, heterocyclyl, heterocyclyl-alkyl, heteroaryl, or heteroaryl-alkyl, and further wherein R8 may be optionally substituted, as defined herein.

[0059] The term “sulfonyl” refers to the group -S(O)2-R8, wherein R8 is hydrogen, alkyl, alkenyl, alkynyl, alkoxy, thioalkyl, aryl, aryl-alkyl, cycloalkyl, cycloalkyl-alkyl, haloalkyl, heterocyclyl, heterocyclyl-alkyl, heteroaryl, or heteroaryl-alkyl, and further wherein R8 may be optionally substituted, as defined herein. “Sugar moiety” refers to a monovalent radical of a sugar molecule, such as a monosaccharide molecule, including glucose (also known as dextrose), fructose, galactose, mannose, allose, altrose, gulose, idose, and talose. As used herein, a sugar moiety a heterocyclyl substituted with OH and / or hydoxyalkyl groups. However, it is understood that a sugar moiety can exist in a liner form as an alkyl substituted with oxo and OH groups.

[0060] The terms “optional” or “optionally” means that the subsequently described event or circumstance may or may not occur and that the description includes instances where said event or circumstance occurs and instances in which it does not. Also, the term “optionally substituted” refers to any one or more (e.g., 1 to 5 or 1 to 3) hydrogen atoms on the designated atom or group may or may not be replaced by a moiety other than hydrogen.

[0061] In certain embodiments, “substituted” includes any of the above alkyl, heteroalkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl or heteroaryl groups in which one or more (e.g., 1 to 5 or 1 to 3) hydrogen atoms are independently replaced with halo, cyano, nitro, azido, oxo, alkyl, alkenyl, alkynyl, haloalkyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, -NR8Rh, -C(NR8)Rh, -C(NR8)(NRh2), -NR8C(=O)Rh, -NR8C(=O)NR8Rh, -NR8C(=O)ORh, -NR8S(=O)i2Rh, -C(=O)R8, -C(=O)OR8, -OC(=O)OR8, -OC(=O)R8, -C(=O)NR8Rh, -OC(=O)NR8Rh, -OR8, -SR8, -S(=O)R8, -S(=O)2R8, -OS(=O)i2R8, -S(=O)i-2OR8, -NR8S(=O)i2NR8Rh, =NSO2R8, =NOR8, -S(=O)i 2NR8Rh, -CR8(=NOH), -NR8C(=NRh)(NRhRh), -SFs, -SCF3 or -OCF3. In certain embodiments, “substituted” also means any of the above groups in which one or more (e.g., 1 to 5 or 1 to 3) hydrogen atoms are replaced with -C(=O)R8, -C(=O)OR8, -C(=O)NR8Rh, -CH2SO2R8, or -CH2SO2NR8Rh. In the foregoing, each of R8 and R11 is independently hydrogen, alkyl, alkenyl, alkynyl, alkoxy, thioalkyl, aryl, aralkyl, cycloalkyl, cycloalkyl-alkyl, haloalkyl, heterocyclyl, heterocyclyl-alkyl, heteroaryl, and / or heteroaryl-alkyl. In certain embodiments, “substituted” also means any of the above groups in which one or more (e.g., 1 to 5 or 1 to 3) hydrogen atoms are replaced with halo, hydroxy, alkyl, alkylhydroxy, or oxo groups.

[0062] Polymers or similar indefinite structures arrived at by defining substituents with further substituents appended ad infinitum (e.g., a substituted aryl having a substituted alkyl which is itself substituted with a substituted aryl group, which is further substituted by a substituted heteroalkyl group, etc.) are not intended for inclusion herein. Unless otherwise noted, the maximum number of serial substitutions in compounds described herein is three. For example, serial substitutions of substituted aryl groups with two other substituted aryl groups are limited to ((substituted aryl)substituted aryl)substituted aryl. Similarly, the above definitions are not intended to include impermissible substitution patterns (e.g., methyl substituted with 5 fluorines or heteroaryl groups having two adjacent oxygen ring atoms). Such impermissible substitution patterns are well known to the skilled artisan.

[0063] In certain embodiments, as used herein, the phrase “one or more” refers to one to five. In certain embodiments, as used herein, the phrase “one or more” refers to one to three.

[0064] Any compound or structure given herein, is also intended to represent unlabeled forms as well as isotopically labeled forms of the compounds. These forms of compounds may also be referred to as - 13 - “isotopically enriched analogs.” Isotopically labeled compounds have structures depicted herein, except that one or more atoms are replaced by an atom having a selected atomic mass or mass number. Examples of isotopes that can be incorporated into the disclosed compounds include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, chlorine and iodine, such as 2H, 3H, nC, 13C, 14C, 13N, 15N, 15O, 17O, 180,31P, 32P, 35S, 18F, 36C1, 123I, and 125I, respectively. Various isotopically labeled compounds of the present disclosure, for example those into which radioactive isotopes such as 3H and 14C are incorporated. Such isotopically labelled compounds may be useful in metabolic studies, reaction kinetic studies, detection or imaging techniques, such as positron emission tomography (PET) or single-photon emission computed tomography (SPECT) including drug or substrate tissue distribution assays or in radioactive treatment of subjects.

[0065] The term “isotopically enriched analogs” includes “deuterated analogs” of compounds described herein in which one or more hydrogens is / are replaced by deuterium, such as a hydrogen on a carbon atom. Such compounds may exhibit increased resistance to metabolism and are thus useful for increasing the half-life of any compound when administered to a mammal, particularly a human. See, for example, Foster, “Deuterium Isotope Effects in Studies of Drug Metabolism,” Trends Pharmacol. Sci. 5(12):524-527 (1984). Such compounds are synthesized by means well known in the art, for example by employing starting materials in which one or more hydrogens have been replaced by deuterium.

[0066] Deuterium labelled or substituted therapeutic compounds of the disclosure may have improved DMPK (drug metabolism and pharmacokinetics) properties, relating to distribution, metabolism and excretion (ADME). Substitution with heavier isotopes such as deuterium may afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life, reduced dosage requirements and / or an improvement in therapeutic index. An 18F, 3H, nC labeled compound may be useful for PET or SPECT or other imaging studies. Isotopically labeled compounds of this disclosure can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.

[0067] The concentration of such a heavier isotope, specifically deuterium, may be defined by an isotopic enrichment factor. In the compounds of this disclosure any atom not specifically designated as a particular isotope is meant to represent any stable isotope of that atom. Unless otherwise stated, when an atom is represented by its name or letter symbol, such as, H, C, O, or N, it is understood that the atom has its natural abundance isotopic composition. For example, when a position is designated specifically as “H” or “hydrogen”, the position is understood to have hydrogen at its natural abundance isotopic composition. Accordingly, in the compounds of this disclosure any atom specifically designated as a deuterium (D) is meant to represent deuterium.

[0068] In many cases, the compounds of this disclosure are capable of forming acid and / or base salts by virtue of the presence of amino and / or carboxyl groups or groups similar thereto.

[0069] Provided also are a pharmaceutically acceptable salt, isotopically enriched analog, deuterated analog, stereoisomer, and mixture of stereoisomers of the compounds described herein. “Pharmaceutically acceptable” or “physiologically acceptable” refer to compounds, salts, compositions, dosage forms and other materials which are useful in preparing a pharmaceutical composition that is suitable for veterinary or human pharmaceutical use.

[0070] The term “pharmaceutically acceptable salt” of a given compound refers to salts that retain the biological effectiveness and properties of the given compound and which are not biologically or otherwise undesirable. “Pharmaceutically acceptable salts” or “physiologically acceptable salts” include, for example, salts with inorganic acids and salts with an organic acid. In addition, if the compounds described herein are obtained as an acid addition salt, the free base can be obtained by basifying a solution of the acid salt. Conversely, if the product is a free base, an addition salt, particularly a pharmaceutically acceptable addition salt, may be produced by dissolving the free base in a suitable organic solvent and treating the solution with an acid, in accordance with conventional procedures for preparing acid addition salts from base compounds. Those skilled in the art will recognize various synthetic methodologies that may be used to prepare nontoxic pharmaceutically acceptable addition salts. Pharmaceutically acceptable acid addition salts may be prepared from inorganic and organic acids. Salts derived from inorganic acids include, e.g., hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like. Salts derived from organic acids include, e.g., acetic acid, propionic acid, gluconic acid, glycolic acid, pyruvic acid, oxalic acid, malic acid, malonic acid, succinic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluene-sulfonic acid, salicylic acid and the like. Salts derived from organic acids may be derived from anhydrous organic acids or hydrates thereof. Likewise, pharmaceutically acceptable base addition salts can be prepared from inorganic and organic bases. Salts derived from inorganic bases include, by way of example only, sodium, potassium, lithium, aluminum, ammonium, calcium and magnesium salts. Salts derived from organic bases include, but are not limited to, salts of primary, secondary and tertiary amines, such as alkyl amines (i.e., NH2(alkyl)), dialkyl amines (i.e., HN(alkyl)2), trialkyl amines (i.e., N(alkyl)3), substituted alkyl amines (i.e., NH2(substituted alkyl)), di(substituted alkyl) amines (i.e., HN(substituted alkyl)2), tri(substituted alkyl) amines (i.e., N(substituted alkyl)?), alkenyl amines (i.e., NH2(alkenyl)), dialkenyl amines (i.e., HN(alkenyl)2), trialkenyl amines (i.e., N(alkenyl)3), substituted alkenyl amines (i.e., NH2(substituted alkenyl)), di(substituted alkenyl) amines (i.e., HN(substituted alkenyl)2), tri(substituted alkenyl) amines (i.e., N(substituted alkenyl)3, mono-, di- or tri- cycloalkyl amines (i.e., NH2(cycloalkyl), HN(cycloalkyl)2, N(cycloalkyl)3), mono-, di- or tri- arylamines (i.e., NH2(aryl), HN(aryl)2, N(aryl)a) or mixed amines, etc. Specific examples of suitable amines include, by way of example only, isopropylamine, trimethyl amine, diethyl amine, tri(iso-propyl) amine, tri(n-propyl) amine, ethanolamine, 2-dimethylaminoethanol, piperazine, piperidine, morpholine, N-ethylpiperidine, and the like.

[0071] Some of the compounds exist as tautomers. Tautomers are in equilibrium with one another. For example, amide containing compounds may exist in equilibrium with imidic acid tautomers. Regardless of which tautomer is shown and regardless of the nature of the equilibrium among tautomers, the compounds are understood by one of ordinary skill in the art to comprise tautomers. Thus, the amide containing compounds are understood to include their imidic acid tautomers. Likewise, the imidic acid containing compounds are understood to include their amide tautomers.

[0072] A “stereoisomer” refers to a compound made up of the same atoms bonded by the same bonds but having different three-dimensional structures, which are not interchangeable. The present invention contemplates various stereoisomers and mixtures thereof and includes “

[0073] Stereoisomers include enantiomers, diastereomers, and other stereoisomeric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)- or, as (D)- or (L)- for amino acids. The present invention is meant to include all such possible isomers, as well as their racemic and optically pure forms. Optically active (+) and (-), (R)- and (S)-, or (D)- and (L)- isomers may be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques, for example, chromatography and fractional crystallization. Conventional techniques for the preparation / isolation of individual enantiomers include chiral synthesis from a suitable optically pure precursor or resolution of the racemate (or the racemate of a salt or derivative) using, for example, chiral high pressure liquid chromatography (HPLC). Stereoisomers also include geometric isomers when the compounds described herein contain olefinic double bonds or other centers of geometric asymmetry. Unless specified otherwise, it is intended that such compounds include both E and Z geometric isomers.

[0074] “Enantiomers” are two stereoisomers whose molecules are non-superimposable mirror images of one another. “Diastereomers” are stereoisomers that have at least two asymmetric atoms, but which are not mirror-images of each other.

[0075] Relative centers of the compounds as depicted herein are indicated graphically using the “thick bond” style and absolute stereochemistry is depicted using wedge bonds.

[0076] When the stereochemistry of a disclosed compound is named or depicted by structure, the named or depicted stereoisomer is at least 60%, 70%, 80%, 90%, 99% or 99.9% by weight pure relative to the other stereoisomers. When a single enantiomer is named or depicted by structure, the depicted or named enantiomer is at least 60%, 70%, 80%, 90%, 99% or 99.9% by weight optically pure. Percent optical purity by weight is the ratio of the weight of the enantiomer over the weight of the enantiomer plus the weight of its optical isomer.

[0077] When the geometry of a disclosed compound is named or depicted by structure, the named or depicted geometrical isomer is at least 60%, 70%, 80%, 90%, 99% or 99.9% by weight pure relative to the other geometrical isomers.

[0078] In certain embodiments, where one or more stereocenters are present, a compound disclosed herein may be provided as a racemic mixture. In certain embodiments, where one or more stereocenters are present, a compound disclosed herein may be provided as a single enantiomer. For example, a compound may be provided in a composition having greater than about 30% ee, about 40% ee, about 50% ee, about 60% ee, about 70% ee, about 80% ee, about 90% ee, about 95% ee, about 97% ee, about 98% ee, about 99% ee, or greater. In certain such embodiments, compounds may be provided in a diastereomerically enriched composition. For example, a diastereomerically enriched composition comprising a compound disclosed herein may have greater than about 30% de, about 40% de, about 50% de, about 60% de, about 70% de, about 80% de, about 90% de, about 95% de, about 97% de, about 98% de, about 99% de, or greater.

[0079] In certain embodiments, the therapeutic preparation may be enriched to provide predominantly one enantiomer of a compound (e.g., of Formula (I)). An enantiomerically enriched mixture may comprise, for example, at least about 60 mol percent of one enantiomer, or more preferably at least about 75, about 90, about 95, or even about 99 mol percent. In certain embodiments, the compound enriched in one enantiomer is substantially free of the other enantiomer, wherein substantially free means that the substance in question makes up less than about 10%, or less than about 5%, or less than about 4%, or less than about 3%, or less than about 2%, or less than about 1% as compared to the amount of the other enantiomer, e.g., in the composition or compound mixture. For example, if a composition or compound mixture contains about 98 grams of a first enantiomer and about 2 grams of a second enantiomer, it would be said to contain about 98 mol percent of the first enantiomer and only about 2% of the second enantiomer.

[0080] In certain embodiments, the therapeutic preparation may be enriched to provide predominantly one diastereomer of a compound (e.g., of Formula (I)). A diastereomerically enriched mixture may comprise, for example, at least about 60 mol percent of one diastereomer, or more preferably at least about 75, about 90, about 95, or even about 99 mol percent.

[0081] The term "subject" to which administration is contemplated includes, but is not limited to, humans (i.e., a male or female of any age group, e.g., a pediatric subject (e.g., infant, child, adolescent) or adult subject (e.g., young adult, middle-aged adult or senior adult)) and / or other primates (e.g., cynomolgus monkeys, rhesus monkeys); mammals, including commercially relevant mammals such as cattle, pigs, horses, sheep, goats, cats, and / or dogs; and / or birds, including commercially relevant birds such as chickens, ducks, geese, quail, and / or turkeys. In one embodiment, the subject is human.

[0082] As used herein, a therapeutic that “prevents” a disorder or condition refers to a compound that, in a statistical sample, reduces the occurrence of the disorder or condition in the treated sample relative to an untreated control sample, or delays the onset or reduces the severity of one or more symptoms of the disorder or condition relative to the untreated control sample.

[0083] The term “treating” means to decrease, suppress, attenuate, diminish, arrest, or stabilize the development or progression of a disease (e.g., a disease or disorder delineated herein), lessen the severity of the disease or improve the symptoms associated with the disease. Treatment includes treating a symptom of a disease, disorder or condition. If it is administered prior to clinical manifestation of the unwanted condition (e.g., disease or other unwanted state of the subject) then the treatment is prophylactic (i.e., it protects the subject against developing the unwanted condition), whereas if it is administered after manifestation of the unwanted condition, the treatment is therapeutic, (i.e., it is intended to diminish, ameliorate, or stabilize the existing unwanted condition or side effects thereof).

[0084] “Pathogenic blood vessels” are blood vessels that are not involved in the vascularization of normal organs but, instead, are involved in vascularization of diseased tissues, such as the new blood vessels that drive vision diseases or the new blood vessels in tumors that tumors depend on to survive. “Pathogenic blood vessel,” in some embodiments, refers to an existing blood vessel that may have vascularized a diseased tissue, for instance, a tumor. In other embodiments, a pathogenic blood vessel may be a blood vessel that is a newly formed blood vessel involved in disease onset and / or progression of, for example, cancer, diabetic retinopathy, age-related macular degeneration (AMD), retinopathy of prematurity and / or any other diseases having etiologies associated with angiogeneis.

[0085] Abbreviations: DCM dichloromethane DIPEA diisopropylethylamine DMA dimethylacetamide DMAP dimethylaminopyridine DMF dimethylformamide DMSO dimethyl sulfoxide EDCI l-ethyl-3-(3-dimethylaminopropyl)carbodiimide Equiv or eq equivalent ESI electrospray ionization EtOAc ethyl acetate EtOH ethanol EtONa sodium ethoxide HOAc or AcOH acetic acid HOBt 1 -hydroxybenzotriazole HPLC high performance liquid chromatography HRMS high-resolution mass spectrometry LC liquid chromatography LCMS liquid chromatography-mass spectrometry mCPBA meta-chloroperoxybenzoic acid MeOH methanol NMM N-methylmorpholine NMP N-methyl-2-pyrrolidone OXONE® Potassium peroxymonosulfate mPEG methoxypoly(ethylene glycol) rt room temperature TEA triethylamine THF tetrahydrofuran TLC thin-layer chromatography TsOH p-toluenesulfonic acid PPSE Trimethylsilyl polyphosphate 2. Compounds

[0086] In certain embodiments, provided is a compound of Formula (I): R8                                  (I), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein n is 0, 1, 2, 3 or 4; R1 is selected from optionally substituted amino, optionally substituted aryl, optionally substituted cycloalklyl, optionally substituted heterocyclyl, and optionally substituted heteroaryl; R2 is selected from H, halo, alkyl, alkenyl, alkynyl, -OH, alkoxy, -CN, -NO2, alkylthio, sulfoxido, sulfonyl, and amino; R5, R7 and R8 are each independently selected from H, halo, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, alkenoxy, alkynoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, and amido; R6 is selected from H, halo, alkyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, amido, sulfinamido, sulfonamido, optionally substituted heterocyclyl, optionally substituted heteroaryl, poly(ethylene glycol), and methoxypoly(ethylene glycol), or R6 and R7 together with atoms to which they are attached form an optionally substituted cycloalkyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl; and each R9 is independently selected from halo, alkyl, -OH, alkoxy, -CN, and amino.

[0087] In certain embodiments, when R2 is C1-6 alkyl, R6 is not C1-6 alkyl or C1-6 alkoxy. In other embodiments, when R2 is C1-3 alkyl, R6 is not C1-3 alkyl or C1-3 alkoxy. In certain embodiments, when R2 is ethyl, then R6 is not methyl or methoxy.

[0088] In certain embodiments, provided is a compound of Formula (I): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein n is 0, 1, 2, 3 or 4; R1 is selected from optionally substituted amino, optionally substituted aryl, optionally substituted cycloalkyl, optionally substituted heterocyclyl, and optionally substituted heteroaryl; R2 is selected from halo, alkyl, alkenyl, alkynyl, alkoxy, alkenoxy, alkynoxy, -CN, and -NO2; R5, R7 and R8 are each independently selected from H, halo, alkyl, alkenyl, hydroxy, and alkoxy; R6 is selected from halo, alkyl, alkenyl, alkynyl hydroxy, alkoxy, alkylthio, sulfoxide, sulfonyl, carboxy, ester, -NO2 -CN, amino, and amido; and each R9 is independently selected from halo, hydroxy, and alkoxy.

[0089] In certain embodiments of Formula (I): n is 0 or 1; R1 is selected from optionally substituted amino, optionally substituted heterocyclyl, and optionally substituted heteroaryl; R2 is selected from alkyl, alkoxy, alkenoxy, alkynoxy, -CN, and -NO2; R5, R7 and R8 are each independently selected from H and alkoxy; R6 is selected from halo, alkyl, alkoxy, sulfoxido, sulfonyl, carboxy, ester, -NO2 and amido; and each R9 is independently halo or alkoxy.

[0090] In certain embodiments, provided is a compound of Formula (I): R8                                  (I), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein n is 0 or 1; R1 is selected from amino, optionally substituted amino heterocyclyl, and optionally substituted amino heteroaryl; R2 is selected from alkyl, alkoxy, -CN, and -NO2; R5, R7 and R8 are each independently selected from H and alkoxy; R6 is selected from halo, alkyl, alkoxy, sulfoxido, sulfonyl, carboxy, ester, -NO2 and amido; and each R9 is independently halo or alkoxy.

[0091] In certain embodiments, the compound of Formula (I) described above has at least one of the following: 1) R2 is selected from C2 aoalkyl, -OH, Ci-4oalkoxy, Ci-4oalkenoxy, Ci-4oalkynoxy, -NO2, alkylthio, sulfoxido, sulfonyl, and amino, where a) when R2 is ethyl, then R6 is not methyl or methoxy, and / or b) when R2 is methoxy, then R6 is not halo, C1-2 alkyl or C1-2 alkoxy; 2) R1 is optionally substituted amino heteroaryl, optionally substituted amino bridged heterocyclyl, optionally substituted amino fused heterocyclyl, or optionally substituted amino cycloheptyl; 3) R1 is heterocyclyl optionally substituted with one halo, amino, hydroxy, alkoxy, -CN, -NO2, alkyl, carboxy, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, optionally substituted cycloalkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, poly(ethylene glycol), or methoxypoly(ethylene glycol), where if the substituent is alkyl, the alkyl is further substituted with one substituent selected from halo, amino, alkoxy, -CN, -NO2, carboxy, ester, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, cycloalkyl, heterocyclyl, poly(ethylene glycol), methoxypoly(ethylene glycol), pyrrolidinyl and piperidinyl; or the alkyl is substituted with at least one -OR31, wherein R31 is poly(ethylene glycol) or methoxypoly(ethylene glycol); 4) R1 is amino substituted with at least one substituent selected from alkyl, cycloalkyl, heterocyclyl, heteroaryl, poly(ethylene glycol) or methoxypoly(ethylene glycol) and amino, where the alkyl is substituted with at least one substituent selected from halo, amino, hydroxy, alkoxy, -CN, -NO2, amido, carboxy, ester, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, cycloalkyl, heterocyclyl, and heteroaryl; or 5) R6 is alkyl substituted with at least one substituent selected from halo, amino, hydroxy, alkoxy, cycloalkoxy, heterocycloalkoxy, aryloxy, heteroaryloxy, poly(ethylene glycol)-oxy, methoxypoly(ethylene glycol)-oxy, -CN, -NO2, oxo, amido, carboxy, ester, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, heterocyclyl, cycloalkyl, aryl, heteroaryl, poly(ethylene glycol) and methoxypoly(ethylene glycol).

[0092] In certain embodiments, provided is a compound of Formula (I'): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein n is 0, 1, 2, 3 or 4; R1 is selected from amino, heterocyclyl, and heteroaryl; R2 is selected from H, halo, alkyl, alkenyl, alkynyl, -OH, alkoxy, -CN, -NO2, alkylthio, sulfoxido, sulfonyl, and amino; R5, R7 and R8 are each independently selected from H, halo, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, and amido; R6 is selected from H, halo, alkyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, amido, sulfinamido, sulfonamido, heterocyclyl, heteroaryl, poly(ethylene glycol), and methoxypoly(ethylene glycol), or R6 and R7 together with atoms to which they are attached form a cycloalkyl, heterocyclyl, aryl, or heteroaryl; and each R9 is independently selected from halo, alkyl, -OH, alkoxy, -CN, and amino.

[0093] In certain embodiments, when R2 is Ci-6 alkyl, R6 is not Ci-6 alkyl or Ci-6 alkoxy. In other embodiments, when R2 is C1-3 alkyl, R6 is not C1-3 alkyl or C1-3 alkoxy. In certain embodiments, when R2 is ethyl, then R6 is not methyl or methoxy.

[0094] In certain embodiments, provided is a compound of Formula (I'): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein n is 0, 1, 2, 3 or 4; R1 is selected from amino, aryl, cycloalkyl, heterocyclyl, and heteroaryl; R2 is selected from halo, alkyl, alkenyl, alkynyl, alkoxy, -CN, and -NO2; R5, R7 and R8 are each independently selected from H, halo, alkyl, alkenyl, hydroxy, and alkoxy; R6 is selected from halo, alkyl, alkenyl, alkynyl hydroxy, alkoxy, alkylthio, sulfoxide, sulfonyl, carboxy, ester, -NO2 -CN, amino, and amido; and each R9 is independently selected from halo, hydroxy, and alkoxy.

[0095] In certain embodiments, provided is a compound of Formula (I'): R8                                    (I'), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein n is 0 or 1; R1 is selected from amino, heterocyclyl, and heteroaryl; R2 is selected from alkyl, alkoxy, -CN, and -NO2; R5, R7 and R8 are each independently selected from H and alkoxy; R6 is selected from halo, alkyl, alkoxy, sulfoxido, sulfonyl, carboxy, ester, -NO2 and amido; and each R9 is independently halo or alkoxy.

[0096] In certain embodiments, the compound of Formula (I') described above has at least one of the following: 1) R2 is selected from C2 aoalkyl, -OH, Ci aoalkoxy, -NO2, alkylthio, sulfoxido, sulfonyl, and amino, where a) when R2 is ethyl, then R6 is not methyl or methoxy, and / or b) when R2 is methoxy, then R6 is not halo, C1-2 alkyl or C1-2 alkoxy; 2) R1 is heteroaryl, bridged heterocyclyl, fused heterocyclyl, or cycloheptyl; 3) R1 is heterocyclyl substituted with one halo, amino, hydroxy, alkoxy, -CN, -NO2, alkyl, carboxy, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, cycloalkyl, heterocyclyl, heteroaryl, poly(ethylene glycol), and methoxypoly(ethylene glycol), where if the substituent is alkyl, the alkyl is further substituted with one substituent selected from halo, amino, alkoxy, -CN, -NO2, carboxy, ester, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, cycloalkyl, heterocyclyl, poly(ethylene glycol), methoxypoly(ethylene glycol), pyrrolidinyl and piperidinyl; or the alkyl is substituted with at least one -OR31, wherein R31 is poly(ethylene glycol) or methoxypoly(ethylene glycol); 4) R1 is amino substituted with at least one substituent selected from alkyl, cycloalkyl, heterocyclyl, heteroaryl, poly(ethylene glycol) or methoxypoly(ethylene glycol) and amino, where the alkyl is substituted with at least one substituent selected from halo, amino, hydroxy, alkoxy, -CN, -NO2, amido, carboxy, ester, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, cycloalkyl, heterocyclyl, and heteroaryl; or 5) R6 is alkyl substituted with at least one substituent selected from halo, amino, hydroxy, alkoxy, cycloalkoxy, heterocycloalkoxy, aryloxy, heteroaryloxy, poly(ethylene glycol)-oxy, methoxypoly(ethylene glycol)-oxy, -CN, -NO2, oxo, amido, carboxy, ester, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, heterocyclyl, cycloalkyl, aryl, heteroaryl, poly(ethylene glycol) and methoxypoly(ethylene glycol).

[0097] In certain embodiments, R1 is heterocyclyl substituted with at least one substituent selected from oxo, - OH, -OR28, -N(R28)2, alkyl, aryl, and heterocyclyl, wherein the alkyl is substituted with at least one substituent selected from -N(R31)2, -S(0)o 2NR31R31, -C(O)N(R31)2, heterocyclyl, cycloalkyl, pyrrolidinyl and piperidinyl; or the alkyl is substituted with at least one -OR31a, wherein R31a is poly(ethylene glycol) or methoxypoly(ethylene glycol); and each R28 and R31 are independently H or alkyl.

[0098] In certain embodiments, R1 is heterocyclyl substituted with at least one substituent selected from oxo, - OH, -OR28, -N(R28)2, - C(O)OR28, alkyl, aryl, and heterocyclyl, wherein the alkyl is substituted with at least one substituent selected from -OH, -N(R31)2, -S(0)o 2NR31R31, -C(O)N(R31)2, heterocyclyl, cycloalkyl, pyrrolidinyl and piperidinyl; or the alkyl is substituted with at least one - OR31a, wherein R31a is poly(ethylene glycol) or methoxypoly(ethylene glycol); and each R28 and R31 are independently H or alkyl.

[0099] In certain embodiments, R1 is -NR3R4, and R3 is H or alkyl unsubstituted or substituted with at least one substituent selected from -OH, -N(R28)2, and heteroaryl, and R4 and R28 are each independently H or alkyl.

[0100] In certain embodiments, R1 is -NR3R4, and R3 is H or alkyl unsubstituted or substituted with at least one substituent selected from -OH, -N(R28)2, aryl, and heteroaryl, and R4 and R28 are each independently H or alkyl.

[0101] In certain embodiments, a compound of Formula (I), or a compound of Formula I and subformulae thereof, refers to a compound of Formula (I), and / or Formula (I'), and / or Formula (II) and / or (Formula III) and / or Formula (IV) and / or (Formula V) and / or Formula (VI) and / or Formula (VII) and / or Formula (VIII) and / or Formula (IX) and / or Formula (X) and / or Formula (XI) and / or Formula (XII), as described herein, or any combination thereof.

[0102] In certain embodiments, provided is a compound of Formula (II): R8                                  (II), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of R1, R2, R5, R6, R7, and R8 is as defined herein.

[0103] In certain embodiments, provided is a compound of Formula (III): R8                                  (III), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of R1, R2, R5, R6, R7, R8 and R9 is as defined herein.

[0104] In certain embodiments, provided is a compound of Formula (IV): (IV), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of R1, R2, R5, R6, R7, R8 and R9 is as defined herein.

[0105] In certain embodiments, R1 is heteroaryl or heterocyclyl, each optionally substituted with a second heterocyclyl, wherein the second heterocyclyl is unsubstituted or substituted with one or more substituents, e.g., selected from -OH, -C(O)Oalkyl, -C(O)NHalkyl, alkyl, aryl, and heterocyclyl; wherein the alkyl and heterocyclyl are each unsubstituted or substituted with one or more substituents selected from -OH, alkyl and aryl.

[0106] In certain embodiments, R1 is heteroaryl, such as a 5- or 6-membered heteroaryl. In certain embodiments, R1 is heterocyclyl, such as a 5- to 9-membered heterocyclyl, a 5- to 7-membered heterocyclyl, or a 5- to 6-membered heterocyclyl.

[0107] In certain embodiments, R1 is heterocyclyl, such as optionally substituted 5- to 7-membered heterocyclyl. In certain embodiments, one of the heterocyclyl substituents is optionally further substituted with a second substituent selected from C3 io cycloalkyl and heterocyclyl. In some embodiments, one heterocyclyl substituent is a sugar moiety, e.g., a hexose. In certain embodiments, one of the second substituents is C310 cycloalkyl or 5- to 7-membered heterocyclyl. In certain embodiments, one second substituent is 5- to 7-membered heterocyclyl. In some embodiments, one second substituent is a sugar moiety, e.g., a hexose.

[0108] In certain embodiments, at least one heterocyclyl substituent is 5- to 7-membered heterocyclyl. In certain embodiments, at least one second substituent is selected from C1-30 alkyl, 5- to 7-membered heterocyclyl, and phenyl.

[0109] In certain embodiments, R1 is 5- to 7-membered heterocyclyl optionally substituted with one or two substituents, wherein at least one substituent is C1-30 alkyl. In certain embodiments, R1 is 5- to 7-membered heterocyclyl optionally substituted with one or two substituents, wherein at least one substituent is 5- to 7-membered heterocyclyl. In some embodiments, the 5- to 7-membered heterocyclyl substituent is further substituted with a sugar moiety, e.g., hexose.

[0110] In certain embodiments, R1 is I I » / ww     OX' uww wherein each s and t is independently 0, 1, 2 or 3, provided that the sum of s and t is 1, 2, 3, or 4; R20 is selected from alkyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl; and R20a is H, NH2, or OH.

[0111] In certain embodiments, R1 is substituted by ^ch3 ? x / W\ 0. .0. / CH, N I V « / w 9 CH, CH3 OH               / OH °-O^0H Q 0666^6 0 6 N N N          N        N N O. •OH h3c. -N H3C H0? o 0 6 a" 6 6 6 °" O 0 \                     IX             IX             N             |\|                       ■■                 ,              IX                          .                 | 06666 6 66 66 ‘OmPEG ch3 h3c N CH '3 H3CV / CH3 66 606 0 06 6

[0112] In certain embodiments, R1 is selected from: HN I HO H3C. / CH3 CH3 I -J HO NH •OH h3c 0 ^N' I JW 9 ^CH3 / N^CH3 HN^ HO HO.          ' CH3 J ^NH NH I 7 ch3 | CH3 HN^ ^CH3 HN^CH3^CH3 «A / W         JWV      JWV      JWV           JWV       ^WV    ^WV    JWV    » / wv         ^vw ^VW    « / VW          UWV     JWV    « / WV    JWV       JWV      % / VW     JWV        JWV CH, OH JWV       « / VW        v / WV JWV    . / VW    » / VW    « / VW    « / WV    WW

[0114] In certain embodiments, R1 is selected from

[0115] In certain embodiments, R1 is selected from

[0116] In certain embodiments, R1 is selected from » / WV    » / WV    » / VW    JWV         JWV      JVW    « / VW    UWV          % / WV      JWV    JWV

[0117] In certain embodiments, R2 is selected from Ci-6 alkyl, -NO2, -OR18, and CN, wherein R18 is selected from Cm6 alkyl, Cighaloalkyl, and C1-6 aminoalkyl. In certain embodiments, R2 is selected from -CH3, -CH2CH3, -CN, -NO2, -OCF3, and -OR18.

[0118] In certain embodiments, R2 is -O(CH2)mCH3, wherein m is an integer selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 12, 13, 14, 15, and 16.

[0119] In certain embodiments, R2 is amino. In some embodiments, the amino is substituted with one or more substituents selected from alkyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, and amino. In certain embodiments, the amino substituent is selected from cyclohexyl, piperazinyl, piperidinyl, and morpholinyl. In certain embodiments, the amino substituent is alkyl substituted with at least one substituent selected from -C(O)OH, -OH, phenyl and pyridyl, and the phenyl and pyridyl are each independently unsubstituted or substituted with halo, alkyl or OH.

[0120] In certain embodiments, R6 is selected from halo, alkyl, -OR17, -S(0)o 2R16, -C(O)OR15, -NO2, and -C(O)NR15R15; R15 is selected from H, methyl, ethyl, iPr, -CH2CH2NEt2, and -CH2CH2OH; R16 is methyl; and R17 is selected from methyl, trifluoromethyl and butyl.

[0121] In certain embodiments, R6 is halo, alkoxy or alkyl. In certain embodiments, R6 is F, alkyl or alkoxy. In certain embodiments, R6 is -OR17, and R17 is haloalkyl. In certain embodiments, R6 is selected from -CH2CN, -OCF3 and NO2.

[0122] In certain embodiments, R6 is -SCH3, -SOCH3, or -SO2CH3. In certain embodiments, R6 is -S(0)o-2R16. In certain embodiments, R6 is -S(O)R16. In certain embodiments, R6 is -S(O)2R16. In _                                 O’ 9                                       T certain embodiments, R6 is r16 r . In certain embodiments, R6 is           .

[0123] In certain embodiments, R6 is -C(O)OR15 where R15 is H or alkyl.. In certain embodiments, R6 is -C(O)OH, -C(O)OCH3 or -C(O)OCH2CH3.

[0124] In certain embodiments, R6 is -C(O)NR15R15. In certain embodiments, each R15 is independently selected from H, alkyl, and heterocyclyl. In other embodiments, R6 is

[0125] In certain embodiments, one R15 is a sugar moiety. In certain embodiments, one R16 is a sugar moiety. In certain embodiments, R6 is a sugar moiety. In certain embodiments, one or more of R6, R15, and R16 is a hexose.

[0126] In certain embodiments, R6 is selected from

[0127] In certain embodiments, provided is a compound of Formula (V): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of s, t, u, and v is independently 0, 1,2, or 3, provided that the sum of s and t is 1, 2, 3 or 4, and the sum of u and v is 1, 2, 3 or 4; w is 0, 1, 2, or 3; Z1 is C or N, when Z1 is C, R20a is H, halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(O)0-2R28, -NHS(O)0-2R28, -S(O)0-2NHR28, -NHS(O)0 2NHR28, -C(O)NH2, -C(O)NHR28, -C(O)N(R28)2, -NHC(O)R28, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, poly(ethylene glycol), methoxypoly(ethylene glycol), C1-30 alkyl optionally substituted with OH or -C(O)OH, or Ci-30 heteroalkyl optionally substituted with OH or -C(O)OH, wherein R32 is H or C1-4 alkyl, and R28 is Cm alkyl; when Z1 is N, R20a is absent; Z2 is C or N; Z3 is CH2, CHR25, CR25R25, or NR25, O, or S(0)o 2 and R25 is selected from H and alkyl; and each of n, R2, R5, R6, R7, R8, and R9 is as defined herein.

[0128] In certain embodiments, provided is a compound of Formula (V): R8                          (V), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of s, t, u, and v is independently 0, 1,2, or 3, provided that the sum of s and t is 1, 2, 3 or 4, and the sum of u and v is 1, 2, 3 or 4; w is 0, 1, 2, or 3; Z1 is C or N, when Z1 is C, R20a is H, halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(O)0-2R28, -NHS(O)0-2R28, -S(O)0-2NHR28, -NHS(O)0 2NHR28, -C(O)NH2, -C(O)NHR28, -C(O)N(R28)2, -NHC(O)R28, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, poly(ethylene glycol), methoxypoly(ethylene glycol), C1-30 alkyl optionally substituted with OH or -C(O)OH, or Ci-30 heteroalkyl optionally substituted with OH or -C(O)OH, wherein R32 is H or Cm alkyl, and R28 is Cm alkyl; when Z1 is N, R20a is absent; Z2 is C or N; Z3 is CH2, CHR25, CR25R25, or NR25, O, or S(0)o 2 and R25 is selected from H and alkyl; n is 0, 1, 2, 3 or 4; R2 is selected from H, halo, alkyl, alkenyl, alkynyl, -OH, alkoxy, -CN, -NO2, alkylthio, sulfoxido, sulfonyl, and amino; R5, R7 and R8 are each independently selected from H, halo, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, and amido; R6 is selected from H, halo, alkyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, amido, sulfinamido, sulfonamido, heterocyclyl, heteroaryl, poly(ethylene glycol), and methoxypoly(ethylene glycol), or R6 and R7 together with atoms to which they are attached form a cycloalkyl, heterocyclyl, aryl, or heteroaryl; and each R9 is independently selected from halo, alkyl, -OH, alkoxy, -CN, and amino.

[0129] In certain embodiments, s is 0 and t is 0. In certain embodiments, s is 0 and t is 1. In certain embodiments, s is 1 and t is 1. In certain embodiments, s is 2 and t is 1. In certain embodiments, s is 3 and t is 1. In certain embodiments, s is 2 and t is 2.

[0130] In certain embodiments, w is 0. In certain embodiments, w is 1. In certain embodiments, w is 2. In certain embodiments, w is 3.

[0131] In certain embodiments, u is 0 and v is 0. In certain embodiments, u is 0 and v is 1. In certain embodiments, u is 1 and v is 1. In certain embodiments, u is 2 and v is 1. In certain embodiments, u is 3 and v is 1. In certain embodiments, s is 2 and u is 2.

[0132] In certain embodiments, provided is a compound of a formula (VI): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of n, s, u, v, R2, R5, R6, R7, R8, R9, R20a, Z2, and Z3 is as defined herein.

[0133] In certain embodiments, provided is a compound of a formula (VII): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of n, s, u, v, R2, R5, R6, R7, R8, R9, and Z3 is as defined herein.

[0134] In certain embodiments, provided is a compound of a formula (VIII): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of n, s, u, v, R2, R5, R6, R7, R8, R9, R20a, Z2, and Z3 is as defined herein.

[0135] In certain embodiments, provided is a compound of a formula (IX): R8                           (IX) or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of n, s, u, v, R2, R5, R6, R7, R8, R9, Z2, and Z3 is as defined herein.

[0136] In certain embodiments, provided is a compound of a formula (X): R8                           (X) or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of n, s, u, v, R2, R5, R6, R7, R8, R9, R20a, Z2, and Z3 is as defined herein.

[0137] In certain embodiments, provided is a compound of a formula (XI): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of n, s, u, v, R2, R5, R6, R7, R8, R9, Z2, and Z3 is as defined herein.

[0138] In certain embodiments, provided is a compound of Formula (I): R8                                  (I), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein R2 is -OC4 30 alkyl; and each of n, R1, R5, R6, R7, R8, and R9 is as defined herein.

[0139] In certain embodiments, provided is a compound of Formula (I): (I), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein R6 is -NO2, ester, amido, alkylthio, sulfoxido, or sulfonyl; and - 39 - each of n, R1, R5, R5, R7, R8, R9 is as defined herein.

[0140] In certain embodiments, R9 is -OH or -O-Cuo alkyl. In certain embodiments, each R9 is independently halo. In certain embodiments, n is 1 or 2 and each R9 is independently halo. In certain embodiments, n is 1 or 2 and each R9 is fluoro.

[0141] In certain embodiments, provided is a compound of Formula (I): R8                                (I), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein R1 is selected from -NR3R4, heterocyclyl optionally substituted with one to five R20, and heteroaryl optionally substituted with one to five R21; R2 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R19, Ci-30 heteroalkyl optionally substituted with one to five R19, -OH, -OR18, -CN, -NO2, -NH2, -S(0)o-2R18, and -NRnR18; R3 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21, R4 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), methoxypoly(ethylene glycol), and -NR13R14; R5, R7 and R8 are each independently selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, C1-30heteroalkyl optionally substituted with one to five R29, -OR15, -S(0)o-2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, and -C(O)NR15R15; R6 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, Ci-30 heteroalkyl optionally substituted with one to five R29, -OR17, -S(0)o-2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, -C(O)NR15R15, -NR15C(O)R16, -S(0)o-2NR15R15, -NR15S(0)o-2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol), or R6 and R7 together with atoms to which they are attached form C510 cycloalkyl optionally substituted with one to five R29, heterocyclyl optionally substituted with one to five R29, aryl optionally substituted with one to five R30, or heteroaryl optionally substituted with one to five R30; R9 is independently selected from halo, Ci-s alkyl optionally substituted with one to five R22, -OH, -OR10, -CN, and -NRnR12; n is 0, 1, 2, 3 or 4; R10 is independently selected from Cno alkyl optionally substituted with one to five R22, and C310 cycloalkyl optionally substituted with one to five R22; R11 and R12 are each independently H or C1-6 alkyl optionally substituted with one to five R22; R13 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21; R14 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R15 is independently selected from H, C1-30 alkyl optionally substituted with one to five R23, Ci-3oheteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R16 is selected from C1-30 alkyl optionally substituted with one to five R23, C1-30heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R17 is selected from H, C1-30 alkyl optionally substituted with one to five R27, C1-30 heteroalkyl optionally substituted with one to five R27, C310 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R18 is selected from C1-30 alkyl optionally substituted with one to five R19 and C1-30 heteroalkyl optionally substituted with one to five R19; each R20 is independently selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(0)o-2R28, -NHS(0)o 2R28, -S(0)o-2NHR28, -NHS(O)0 2NHR28, -C(O)NH2, -C(O)NHR28, -C(O)N(R28)2, -NHC(O)R28, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, C1-30 alkyl optionally substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R21 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(0)o-2R28, -NHS(0)o 2R28, -S(0)o-2NHR28, -NHS(O)0 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, C1-6 alkyl optionally substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, and heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R19 or R22 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl, C1-4 haloalkyl, Cm hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-CM alkyl, -NHS(0)o-2-Cm alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-C14 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4 haloalkyl, -N(Ci-4haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(O)^-Ci4 haloalkyl, -NHS(0)o-2-Cm haloalkyl, -S(0)o-2NH-Ci-4haloalkyl, -NHS(0)o 2NH-C1 4 haloalkyl, -C(O)NH-Ci 4 haloalkyl, -NHC(O)-Ci 4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-Ci 4 haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci~4 haloalkyl^, and C310 cycloalkyl; each R25 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, C1-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R26 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, C1-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, and heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R31 is independently selected C1-30 alkyl optionally substituted with one to five R33, Ci-30 heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol) and methoxypoly (ethylene glycol); each R32 is independently selected H and C1-4 alkyl; each R23, R27, R29 or R33 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl optionally substituted with phenyl, Ci-4 haloalkyl, C1-4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-Ci-4 alkyl, -NHS(0)o-2-Ci-4 alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o-2NH-Ci-4 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-Cm haloalkyl, -N(Ci-4 haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(0)o-2-C1-4haloalkyl, -NHS(0)o 2-Ci-4 haloalkyl, -S(0)o 2NH-Ci-4 haloalkyl, -NHS(O)0 2NH-Ci 4 haloalkyl, -C(O)NH-Ci 4 haloalkyl, -NHC(O)-Ci 4 haloalkyl, -C(O)N(Ci-4 haloalkyl)2, -OC(O)NH-Ci 4 haloalkyl, -NHC(O)O-Ci 4haloalkyl, -OC(O)N(Ci-4haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o-4-0-poly(ethylene glycol), methoxypoly(ethylene glycol)-0-(CH2)o-4-, and sugar moiety; each R24, R30 or R34 is independently selected from halo, -NH2, -OH, -CN, -NO2, C1-4 alkyl, C1-4 haloalkyl, Cj4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci 4 alkyl, -C(O)OH, -C(O)O-Ci-4 alkyl, -S(0)o-2-CM alkyl, -NHS(0)o-2-Cm alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-Ci 4 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4 haloalkyl, -N(Ci-4haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(0)o-2-Cm haloalkyl, -NHS(0)o-2-Cm haloalkyl, -S(0)o-2NH-Ci-4haloalkyl, -NHS(0)o 2NH-Ci 4 haloalkyl, -C(O)NH-Ci 4 haloalkyl, -NHC(O)-Ci 4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-Ci 4 haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci-4haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl, heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o-4-0-poly(ethylene glycol), -(CH2)o-4-0-methoxypoly(ethylene glycol) and sugar moiety; and each R28 is independently selected from C1-30 alkyl optionally substituted with one to five R25, Ci-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol).

[0142] In certain embodiments, provided is a compound of Formula (I): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein n is 0, 1, 2, 3 or 4; R1 is selected from -NR3R4, heterocyclyl optionally substituted with one to five R20, and heteroaryl optionally substituted with one to five R21; R2 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R19, Ci-30 heteroalkyl optionally substituted with one to five R19, -OH, -OR18, -CN, -NO2, -S(0)o 2R18, and -NRnR18; R3 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21; R4 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), methoxypoly(ethylene glycol), and -NR13R14; R5, R7 and R8 are each independently selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, C1-30heteroalkyl optionally substituted with one to five R29, -OR15, -S(0)o-2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, and -C(O)NR15R15; R6 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, Ci-30 heteroalkyl optionally substituted with one to five R29, -OR17, -S(0)o 2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, -C(O)NR15R15, -NR15C(O)R16, -S(0)o-2NR15R15, -NR15S(0)o-2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol), or R6 and R7 together with atoms to which they are attached form C510 cycloalkyl optionally substituted with one to five R29, heterocyclyl optionally substituted with one to five R29, aryl optionally substituted with one to five R30, or heteroaryl optionally substituted with one to five R30; R9 is independently selected from halo, Ci-s alkyl optionally substituted with one to five R22, -OH, -OR10, -CN, and -NRnR12; R10 is independently selected from Cno alkyl optionally substituted with one to five R22, and C310 cycloalkyl optionally substituted with one to five R22; R11 and R12 are each independently H or C1-6 alkyl optionally substituted with one to five R22; R13 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21; R14 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R15 is independently selected from H, C1-30 alkyl optionally substituted with one to five R23, Ci-3oheteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R16 is selected from C1-30 alkyl optionally substituted with one to five R23, C1-30heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R17 is selected from H, C1-30 alkyl optionally substituted with one to five R27, C1-30 heteroalkyl optionally substituted with one to five R27, C310 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R18 is selected from C1-30 alkyl optionally substituted with one to five R19 and C1-30 heteroalkyl optionally substituted with one to five R19; each R20 is independently selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(0)o-2R28, -NHS(0)o 2R28, -S(0)o-2NHR28, -NHS(O)0 2NHR28, -C(O)NH2, -C(O)NHR28, -C(O)N(R28)2, -NHC(O)R28, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, C1-30 alkyl optionally substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R21 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(0)o-2R28, -NHS(0)o 2R28, -S(0)o-2NHR28, -NHS(O)0 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, C1-6 alkyl optionally substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, and heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R19 or R22 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl, C1-4 haloalkyl, Cm hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-CM alkyl, -NHS(0)o-2-Cm alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-C14 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4 haloalkyl, -N(Ci-4haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(O)^-Ci4 haloalkyl, -NHS(0)o-2-Cm haloalkyl, -S(0)o-2NH-Ci-4haloalkyl, -NHS(0)o 2NH-C1 4 haloalkyl, -C(O)NH-Ci 4 haloalkyl, -NHC(O)-Ci 4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-Ci 4 haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci~4 haloalkyl^, and C310 cycloalkyl; each R25 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, C1-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, and heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R26 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, C1-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R31 is independently selected C1-30 alkyl optionally substituted with one to five R33, Ci-30 heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol) and methoxypoly (ethylene glycol); each R32 is independently selected H and C1-4 alkyl; each R23, R27, R29 or R33 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl optionally substituted with phenyl, Ci-4 haloalkyl, C1-4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-Ci-4 alkyl, -NHS(0)o-2-Ci-4 alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o-2NH-Ci-4 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-Cm haloalkyl, -N(Ci-4 haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(0)o-2-C1-4haloalkyl, -NHS(0)o 2-C1-4 haloalkyl, -S(0)o 2NH-C1-4 haloalkyl, -NHS(O)0 2NH-C1 4 haloalkyl, -C(O)NH-Ci 4 haloalkyl, -NHC(O)-Ci 4 haloalkyl, -C(O)N(Ci-4 haloalkyl)2, -OC(O)NH-Ci 4 haloalkyl, -NHC(O)O-Ci 4haloalkyl, -OC(O)N(Ci-4haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl, heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o 4-O-poly(ethylene glycol), methoxypoly(ethylene glycol)-0-(CH2)o4-, and sugar moiety; each R24, R30 or R34 is independently selected from halo, -NH2, -OH, -CN, -NO2, C1-4 alkyl, C1-4 haloalkyl, Cj4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)OH, -C(O)O-Ci-4 alkyl, -S(0)o-2-CM alkyl, -NHS(0)o-2-Cm alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-C14 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4haloalkyl, -N(Ci-4haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(O)^-Ci4 haloalkyl, -NHS(0)o-2-Cm haloalkyl, -S(0)o-2NH-Ci-4haloalkyl, -NHS(0)o 2NH-C1 4 haloalkyl, -C(O)NH-Ci 4 haloalkyl, -NHC(O)-Ci 4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-Ci 4 haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci-4 haloalkyl^, C310 cycloalkyl, heterocyclyl, aryl, heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o 4-O-poly(ethylene glycol), -(CH2)o 4-O-methoxypoly(ethylene glycol) and sugar moiety; and each R28 is independently selected from C1-30 alkyl optionally substituted with one to five R25, Ci-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol).

[0143] In certain embodiments, the compound of Formula (I) described above has at least one of the following: (1) R2 is selected from C2 30 alkyl optionally substituted with one to five R19, C1-30heteroalkyl optionally substituted with one to five R19, -NO2, -OR18, -S(0)o 2CH3, -S(0)o-2R18, -NH2, -NHCH3, and -NRnR18, wherein R18 is selected from Cuohaloalkyl, C2 30 alkyl optionally substituted with one to five R19 and C2 30 heteroalkyl optionally substituted with one to five R19; wherein when R2 is ethyl, then R6 is not methyl or methoxy; (2) R1 is heteroaryl optionally substituted with one to five R21, or fused heterocyclyl optionally substituted with one to five R20; (3) R1 is heterocyclyl substituted with at least one R20 selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28a, -NHS(O)0-2R28, -OC(O)R28, -S(0)o-2R28, -S(0)o-2NHR28, -NHS(0)o 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, c1-30 alkyl substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl substituted with one to five R25, heteroaryl optionally substituted with one to five R26, poly (ethylene glycol), and methoxypoly(ethylene glycol); wherein the Ci-30 alkyl is substituted with at least one R25 selected from halo, -NH2, -OH, -CN, -NO2, oxo, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, heterocyclyl substituted with one to five R33, poly(ethylene glycol), methoxypoly(ethylene glycol), pyrrolidinyl and piperidinyl; or the C1-30 alkyl is substituted with at least one -OR31a, wherein R31a is poly(ethylene glycol) or methoxypoly(ethylene glycol); R28a is selected from C1-30 alkyl substituted with one to five R25, C1-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly (ethylene glycol), and methoxypoly (ethylene glycol); (4) R1 is -NR3R4, and R4 is selected from C1-30 alkyl substituted with one to five R20, Ci-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), methoxypoly(ethylene glycol), and -NR13R14, wherein the Ci-30 alkyl is substituted with at least one R20 selected from halo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -S(0)o-2R28, -NHS(0)o-2R28, -S(0)o-2NHR28, -NHS(O)0 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, and heteroaryl optionally substituted with one to five R26; or (5) R6 is selected from C1-6 alkyl substituted with one to five R29, -OR17, -S(0)o 2R16, C(O)OR15, -OC(O)R16, -NO2, -NR15R15, -C(O)NR15R15, -S(O)0-2NHR16, -NHS(O)0-2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol), wherein R17 is selected from Ci-30 alkyl substituted with one to five R27, C1-30 heteroalkyl optionally substituted with one to five R27, C3-10 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol).

[0144] In certain embodiments, R1 is heteroaryl optionally substituted with one to five R21; or R1 is heterocyclyl substituted with at least one R20 selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28a, -NHS(O)0-2R28, -OC(O)R28, -S(0)o-2R28, -S(0)o-2NHR28, -NHS(0)o 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, c1-30 alkyl substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, heterocyclyl substituted with one to five R25, poly(ethylene glycol), and methoxypoly(ethylene glycol); wherein the Ci-so alkyl is substituted with at least one R25 selected from halo, -NH2, -OH, -CN, -NO2, oxo, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, heterocyclyl substituted with one to five R33, poly(ethylene glycol), methoxypoly(ethylene glycol), pyrrolidinyl and piperidinyl; or the C1-30 alkyl is substituted with at least one -OR31, wherein R31 is poly(ethylene glycol) or methoxypoly(ethylene glycol); and R28a is selected from C1-30 alkyl substituted with one to five R25, C1-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly (ethylene glycol), and methoxypoly (ethylene glycol).

[0145] In certain embodiments, R1 is heteroaryl optionally substituted with one to five R21. In certain embodiments, R1 is 5- or 6-membered heteroaryl optionally substituted with one to five R21.

[0146] In certain embodiments, R1 is heterocyclyl optionally substituted with one to two R20. In certain embodiments, R1 is 5- to 7-membered heterocyclyl optionally substituted with one to two R20. In certain embodiments, one of the R20 is optionally substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, or heterocyclyl optionally substituted with one to five R25. In some embodiments, one R20 is a sugar moiety. In certain embodiments, one of the R25 is C310 cycloalkyl optionally substituted with one to five R33, or 5- to 7-membered heterocyclyl optionally substituted with one to five R33. In some embodiments, one R25 is a sugar moiety. In certain embodiments, one of the R33 is 5- to 7-membered heterocyclyl. In some embodiments, one R33 is a sugar moiety.

[0147] In certain embodiments, at least one R20 is 5- to 7-membered heterocyclyl optionally substituted with one to five R25. In certain embodiments, at least one R25 is selected from C1-30 alkyl optionally substituted with one to five R33, 5- to 7-membered heterocyclyl optionally substituted with one to five R33, and phenyl optionally substituted with one to five R34. In some embodiments, one R20 is a sugar moiety.

[0148] In certain embodiments, R1 is 5- to 7-membered heterocyclyl optionally substituted with one to two R20, wherein at least one R20 is C1-30 alkyl optionally substituted with one to five R25. In certain embodiments, R1 is 5- to 7-membered heterocyclyl optionally substituted with one to two R20, wherein at least one R20 is 5- to 7-membered heterocyclyl optionally substituted with one to five R25. In some embodiments, at least one R25 is 5- to 7-membered heterocyclyl optionally substituted with one to five R33. In some embodiments, one R25 is a sugar moiety.

[0149] In certain embodiments, R1 is I % / WW      OX' wherein each s and t is independently 0, 1, 2 or 3, provided that the sum of s and t is 1, 2, 3, or 4, R20 is Ci-30 alkyl substituted with one to five R25, C1-30 heteroalkyl optionally substituted with one to five R25, C3-io cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, and R20a is H, NH2, or OH.

[0150] In certain embodiments, R20 is selected from -S(0)o 2R28, -S(0)o 2NHR28, -NHS(0)o 2NHR28, Ci-30 alkyl substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, and heteroaryl optionally substituted with one to five R26. In some embodiments, one R20 is a sugar moiety.

[0151] In certain embodiments, one of R25 is selected from C1-30 alkyl substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, and heteroaryl optionally substituted with one to five R33. In some embodiments, one R25 is a sugar moiety. In certain embodiments, one of R26 is selected from C1-30 alkyl substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, and heteroaryl optionally substituted with one to five R33. In some embodiments, one R26 is a sugar moiety.

[0152] In certain embodiments, one R21 is a sugar moiety. In certain embodiments, one R28 is a sugar moiety. In certain embodiments, one R31 is a sugar moiety.

[0153] In certain embodiments, one R23, R24, R27, R29, R30, R33 or R34 is a sugar moiety.

[0154] In certain embodiments, both R2 and R6 are other than H. In certain embodiments, when R2 is methyl or ethyl, then R6 is not selected from methyl, ethyl, methoxy or ethoxy.

[0155] In certain embodiments, R2 is selected from C2 30 alkyl optionally substituted with one to five R19, C1-30 heteroalkyl optionally substituted with one to five R19, -NO2, -OR18, -S(0)o 2R18, and -NRnR18, wherein R18 is selected from Ci aohaloalkyl, C2 30 alkyl optionally substituted with one to five R19 and C2 30 heteroalkyl optionally substituted with one to five R19; wherein when R2 is ethyl, then R6 is not methyl or methoxy.

[0156] In certain embodiments, R2 is C2 30 alkyl substituted with one to five R19. In certain embodiments, R2 is C2 30 heteroalkyl substituted with one to five R19. In certain embodiments, R2 is -51 - -O(CH2)mCH3 or -O(CH2)mCH2C(O)OH, wherein m is an integer selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, and 29.

[0157] In certain embodiments, R2 is -NO2. In certain embodiments, R2 is -CN.

[0158] In certain embodiments, R2 is -OR18 or -S(0)o-2R18. In certain embodiments, R18 is Ci 3ohaloalkyl. In certain embodiments, R18 is C2 30 alkyl optionally substituted with one to five R19. In certain embodiments, R18 is C1-30 heteroalkyl optionally substituted with one to five R19.

[0159] In certain embodiments, each R19 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, Cm alkoxy, -NH-Cm alkyl, -N(Cm alkyl)2, -C(0)-Cm alkyl, and -C(O)OH. In certain embodiments, R19 is -C(O)OH.

[0160] In certain embodiments, R2 is C1-30 alkyl, -CN, -NO2 and -OR18. In certain embodiments, R2 is -CH3, -CH2CH3, -NO2, -OCF3, and -OR18. In certain embodiments, R2 is -OR18, wherein R18 is C4 30 alkyl optionally substituted with one to five R19.

[0161] In certain embodiments, R6 is selected from Cm alkyl substituted with one to five R29, -OR17, -S(0)o-2R16, -C(O)OR15, -OC(O)R16, -NO2, -NR15R15, -C(O)NR15R15, -S(O)0-2NHR16, -NHS(0)o 2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol), wherein R17 is selected from C1-30 alkyl substituted with one to five R27, C1-30heteroalkyl optionally substituted with one to five R27, C310 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol).

[0162] In certain embodiments, R6 is a sugar moiety.

[0163] In certain embodiments, R6 is halo, C1-30 alkyl optionally substituted with one to five R29, Ci-30 heteroalkyl optionally substituted with one to five R29, -OR17, -S(0)o 2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, -C(O)NR15R15, -NR15C(O)R16, -S(0)o-2NR15R15, -NR15S(0)o-2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol).

[0164] In certain embodiments, R6 is halo, OR17, or C1-30 alkyl optionally substituted with halo or C(O)OH, wherein R17 is C1-30 alkyl optionally substituted with halo or C(O)OH. In certain embodiments, R6 is F, C1-C4 alkyl or C1-C4 alkoxy. In certain embodiments, R6 is OR17, and R17 is C1-C4 haloalkyl. In certain embodiments, R6 is selected from CH2CN, OCF3 and NO2.

[0165] In certain embodiments, R6 is S(0)o 2R16- In certain embodiments, R16 is C1-C30 alkyl optionally substituted with halo or C(O)OH. In certain embodiments, R6 is SCH3, SOCH3, and SO2CH3. In certain embodiments, R6 is -SCH3, -SOCH3, or -SO2CH3. In certain embodiments, R6 is -S(0)o zR16- In certain embodiments, R6 is -S(O)R16. In certain embodiments, R6 is -S(O)2R16. In _                                 O’ 9                                         I certain embodiments, R6 is r16    * . In certain embodiments, R6 is           .

[0166] In certain embodiments, R6 is C(O)OR15. In certain embodiments, R15 is H or Ci-30 alkyl optionally substituted with halo or C(O)OH. In certain embodiments, R6 is -C(O)OH, -C(O)OCH3 or -C(O)OCH2CH3.

[0167] In certain embodiments, R6 is -C(O)NR15R15. In certain embodiments, one R15 is H or alkyl. In certain embodiments, one R15 is H, Ci-3o alkyl optionally substituted with one to five R23, Ci-3o heteroalkyl optionally substituted with one to five R20, and heterocyclyl optionally substituted with one to five R23.

[0168] In certain embodiments, one R15 is a sugar moiety. In certain embodiments, one R16 is a sugar moiety.

[0169] In certain embodiments, R6 is a sugar moiety.

[0170] In certain embodiments, R6 and R7 together with atoms to which they are attached form Cs io cycloalkyl optionally substituted with one to five R29. In certain embodiments, R6 and R7 together with atoms to which they are attached form heterocyclyl optionally substituted with one to five R29. In certain embodiments, R6 and R7 together with atoms to which they are attached form aryl optionally substituted with one to five R30. In certain embodiments, R6 and R7 together with atoms to which they are attached form heteroaryl optionally substituted with one to five R30. In certain embodiments, one R29 is a sugar moiety. In certain embodiments, one R30 is a sugar moiety.

[0171] In certain embodiments, R5, R7 and R8 are each H. In certain embodiments, R5 and R8 are each H, and R7 is OCH3.

[0172] In certain embodiments, the compound has no more than one group selected from poly(ethylene glycol), methoxypoly (ethylene glycol) and sugar moiety.

[0173] In certain embodiments, both R2 and R6 are other than H. In certain embodiments, when R2 is methyl or ethyl, then R6 is not selected from methyl, ethyl, methoxy or ethoxy.

[0174] In certain embodiments, R2 is selected from C2 3o alkyl optionally substituted with one to five R19, Ci-3o heteroalkyl optionally substituted with one to five R19, -NO2, -OR18, -S(0)o 2R18, and -NRnR18, wherein R18 is selected from Cuohaloalkyl, C2 3o alkyl optionally substituted with one to five R19 and C2 3o heteroalkyl optionally substituted with one to five R19; wherein when R2 is ethyl, then R6 is not methyl or methoxy.

[0175] In certain embodiments, R2 is C2 3o alkyl substituted with one to five R19. In certain embodiments, R2 is C2 3o heteroalkyl substituted with one to five R19. In certain embodiments, R2 is -O(CH2)mCH3 or -O(CH2)mCH2C(O)OH, wherein m is an integer selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, and 29.

[0176] In certain embodiments, R2 is -OR18, wherein R18 is C4 30 alkyl optionally substituted with one to five R19.

[0177] In certain embodiments, R2 is -NO2. In certain embodiments, R2 is -CN.

[0178] In certain embodiments, R2 is -OR18 or -S(0)o-2R18. In certain embodiments, R18 is Cijohaloalkyl. In certain embodiments, R18 is C2 30 alkyl optionally substituted with one to five R19. In certain embodiments, R18 is C1-30 heteroalkyl optionally substituted with one to five R19.

[0179] In certain embodiments, each R19 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, Ci-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, and -C(O)OH. In certain embodiments, R19 is -C(O)OH.

[0180] In certain embodiments, R2 is C1-30 alkyl, -CN, -NO2 and -OR18. In certain embodiments, R2 is -CH3, -CH2CH3, -NO2, -OCF3, and -OR18. In certain embodiments, R2 is -OR18, wherein R18 is C4 30 alkyl optionally substituted with one to five R19.

[0181] In certain embodiments, R6 is selected from C1-6 alkyl substituted with one to five R29, -OR17, -S(0)o-2R16, -C(O)OR15, -OC(O)R16, -NO2, -NR15R15, -C(O)NR15R15, -S(O)0-2NHR16, -NHS(0)o 2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol), wherein R17 is selected from C1-30 alkyl substituted with one to five R27, C1-30heteroalkyl optionally substituted with one to five R27, C310 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol).

[0182] In certain embodiments, R6 is -NO2, -C(O)OR15, -OC(O)R16, -C(O)NR15R15, -NR15C(O)R15, -S(0)o-2R16, -S(0)o-2NHR16, or -NHS(0)o-2R16-

[0183] In certain embodiments, R6 is a sugar moiety.

[0184] In certain embodiments, R6 is halo, C1-30 alkyl optionally substituted with one to five R29, Ci-30 heteroalkyl optionally substituted with one to five R29, -OR17, -S(0)o 2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, -C(O)NR15R15, -NR15C(O)R16, -S(0)o-2NR15R15, -NR15S(0)o-2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol).

[0185] In certain embodiments, R6 is halo, OR17, or C1-30 alkyl optionally substituted with halo or C(O)OH, wherein R17 is C1-30 alkyl optionally substituted with halo or C(O)OH. In certain embodiments, R6 is F, C1-C4 alkyl or C1-C4 alkoxy. In certain embodiments, R6 is OR17, and R17 is C1-C4 haloalkyl. In certain embodiments, R6 is selected from CH2CN, OCF3 and NO2.

[0186] In certain embodiments, R6 is S(0)o zR16- In certain embodiments, R16 is C1-C30 alkyl optionally substituted with halo or C(O)OH. In certain embodiments, R6 is SCH3, SOCH3, and SO2CH3. In certain embodiments, R6 is C(O)OR15. In certain embodiments, R15 is H or Ci-30 alkyl optionally substituted with halo or C(O)OH. In certain embodiments, R6 is -C(O)OH, -C(O)OCH3 or -C(O)OCH2CH3.

[0187] In certain embodiments, R6 is -C(O)NR15R15. In certain embodiments, one R15 is H or alkyl. In certain embodiments, one R15 is H, C1-30 alkyl optionally substituted with one to five R23, Ci-30 heteroalkyl optionally substituted with one to five R20, and heterocyclyl optionally substituted with one to five R23.

[0188] In certain embodiments, one R15 is a sugar moiety. In certain embodiments, one R16 is a sugar moiety.

[0189] In certain embodiments, R6 is a sugar moiety.

[0190] In certain embodiments, R6 is selected from

[0191] In certain embodiments, R6 and R7 together with atoms to which they are attached form C5 10 cycloalkyl optionally substituted with one to five R29. In certain embodiments, R6 and R7 together with atoms to which they are attached form heterocyclyl optionally substituted with one to five R29. In certain embodiments, R6 and R7 together with atoms to which they are attached form aryl optionally substituted with one to five R30. In certain embodiments, R6 and R7 together with atoms to which they are attached form heteroaryl optionally substituted with one to five R30. In certain embodiments, one R29 is a sugar moiety. In certain embodiments, one R30 is a sugar moiety.

[0192] In certain embodiments, R5, R7 and R8 are each H. In certain embodiments, R5 and R8 are each H, and R7 is OCH3.

[0193] In certain embodiments, R1, R6 and R2 are each not H. In certain embodiments, R1, R6, R7, and R2 are each not H.

[0194] In certain embodiments, R2 is -OR18, wherein R18 is C4 30 alkyl optionally substituted with one to five R19; R6 is -NO2, -C(O)OR15, -OC(O)R16, -C(O)NR15R15, -NR15C(O)R15, -S(O)0-2R16, -S(0)o 2NHR16, or -NHS(0)o 2R16; R5, R7 and R8 are each H, or R5 and R8 are each H, and R7 is OCH3.

[0195] In certain embodiments, the compound has no more than one group selected from poly(ethylene glycol), methoxypoly (ethylene glycol) and sugar moiety.

[0196] Provided herein is a compound of Formula (I): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein R1 is selected from -NR3R4, heterocyclyl optionally substituted with one to five R20, and heteroaryl optionally substituted with one to five R21; R2 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R19, C1-30 heteroalkyl optionally substituted with one to five R19, -OH, -OR18, -CN, -NO2, -NH2, -S(0)o 2R18, and -NRnR18; R3 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21, R4 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), methoxypoly(ethylene glycol), and -NR13R14; R5, R7 and R8 are each independently selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, Ci-3o heteroalkyl optionally substituted with one to five R29, -OR15, -S(0)o-2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, and -C(O)NR15R15; R6 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, C1-30 heteroalkyl optionally substituted with one to five R29, -OR17, -S(0)o 2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, -C(O)NR15R15, -NR15C(O)R16, -S(0)o-2NR15R15, -NR15S(0)o-2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol), or R6 and R7 together with atoms to which they are attached form C510 cycloalkyl optionally substituted with one to five R29, heterocyclyl optionally substituted with one to five R29, aryl optionally substituted with one to five R30, or heteroaryl optionally substituted with one to five R30; R9 is independently selected from halo, Ci s alkyl optionally substituted with one to five R22, -OH, -OR10, -CN, and -NRnR12; n is 0, 1, 2, 3 or 4; R10 is independently selected from Cno alkyl optionally substituted with one to five R22, and C3 io cycloalkyl optionally substituted with one to five R22; R11 and R12 are each independently H or C1-6 alkyl optionally substituted with one to five R22; R13 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21; R14 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R15 is independently selected from H, C1-30 alkyl optionally substituted with one to five R23, Ci-30 heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R16 is selected from C1-30 alkyl optionally substituted with one to five R23, C1-30heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R17 is selected from H, C1-30 alkyl optionally substituted with one to five R27, C1-30 heteroalkyl optionally substituted with one to five R27, C310 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R18 is selected from C1-30 alkyl optionally substituted with one to five R19 and C1-30 heteroalkyl optionally substituted with one to five R19; each R20 is independently selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(0)o-2R28, -NHS(0)o 2R28, -S(0)o-2NHR28, -NHS(0)o 2NHR28, -C(O)NH2, -C(O)NHR28, -C(O)N(R28)2, -NHC(O)R28, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, c1-30 alkyl optionally substituted with one to five R25, C1-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R21 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(0)o-2R28, -NHS(0)o 2R28, -S(0)o-2NHR28, -NHS(0)o 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, C1-6 alkyl optionally substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R19 or R22 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl, C1-4 haloalkyl, C1-4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-Ci4 alkyl, -NHS(0)o-2-Ci4 alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-C1 4 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4 haloalkyl, -N(Ci-4 haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(0)o2-Ci-4 haloalkyl, -NHS(0)o 2-Ci-4 haloalkyl, -S(0)o 2NH-C1-4 haloalkyl, -NHS(0)o-2NH-Ci-4 haloalkyl, -C(O)NH-Ci-4haloalkyl, -NHC(O)-Ci-4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-Ci-4haloalkyl, -NHC(O)O-Ci-4haloalkyl, -OC(O)N(Ci-4haloalkyl)2, and C310 cycloalkyl; each R25 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R26 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(O)0-2R31, -NR32S(O)0-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R31 is independently selected C1-30 alkyl optionally substituted with one to five R33, Ci-30 heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol) and methoxypoly(ethylene glycol); each R32 is independently selected H and C1-4 alkyl; each R23, R27, R29 or R33 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl optionally substituted with phenyl, Ci-4haloalkyl, C1-4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-Ci-4 alkyl, -NHS(0)o-2-Ci-4 alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o-2NH-Ci-4 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-Cwhaloalkyl, -N(CM haloalkyl)2, -C(O)-Ci-4haloalkyl, -S(0)o-2-Ci-4haloalkyl, -NHS(0)o-2-Ci-4haloalkyl, -S(0)o-2NH-Ci-4haloalkyl, -NHS(0)o 2NH-Ci-4haloalkyl, -C(O)NH-Ci-4haloalkyl, -NHC(O)-Ci-4haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-CMhaloalkyl, -NHC(O)O-Ci-4haloalkyl, -OC(O)N(Ci 4 haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o4-0-poly(ethylene glycol), methoxypoly(ethylene glycol)-0-(CH2)o 4-, and sugar moiety; each R24, R30 or R34 is independently selected from halo, -NH2, -OH, -CN, -NO2, C1-4 alkyl, C1-4 hydroxyalkyl, Ci-4haloalkyl, Cj4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)OH, -C(O)O-Ci-4 alkyl, -S(0)o-2-Ci-4 alkyl, -NHS(0)o-2-Ci-4 alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-C14 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-Ci-4haloalkyl, -N(Ci-4 haloalkyl)2, -C(O)-Ci-4haloalkyl, -S(0)o2-Ci-4haloalkyl, -NHS(0)o 2-Ci-4haloalkyl, -S(0)o 2NH-C1-4 haloalkyl, -NHS(0)o-2NH-Cm haloalkyl, -C(O)NH-Ci-4 haloalkyl, -NHC(O)-Ci- 4haloalkyl, -C(O)N(Cm haloalkyl)2, -OC(O)NH-Ci-4haloalkyl, -NHC(O)O-Ci-4haloalkyl, -OC(O)N(Ci-4haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl, heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o 4-O-poly(ethylene glycol), -(CH2)o 4-O-methoxypoly(ethylene glycol) and sugar moiety; and each R28 is independently selected from C1-30 alkyl optionally substituted with one to five R25, Ci-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly (ethylene glycol), and methoxypoly(ethylene glycol); provided at least that the compound has at least one of the following: (1) R2 is selected from C2 30 alkyl optionally substituted with one to five R19, C1-30heteroalkyl optionally substituted with one to five R19, -NO2, -OR18, -S(0)o-2R18, and -NRnR18, wherein R18 is selected from Ci-3ohaloalkyl, C2 30 alkyl optionally substituted with one to five R19 and C2 30 heteroalkyl optionally substituted with one to five R19; wherein when R2 is ethyl, then R6 is not methyl or methoxy; (2) R1 is heteroaryl optionally substituted with one to five R21, or fused heterocyclyl optionally substituted with one to five R20; (3) R1 is heterocyclyl substituted with at least one R20 selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28a, -NHS(O)0-2R28, -OC(O)R28, -S(0)o-2R28, -S(0)o-2NHR28, -NHS(0)o 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, c1-30 alkyl substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl substituted with one to five R25, heteroaryl optionally substituted with one to five R26, poly (ethylene glycol), and methoxypoly(ethylene glycol); wherein the Ci-30 alkyl is substituted with at least one R25 selected from halo, -NH2, -OH, -CN, -NO2, oxo, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, heterocyclyl substituted with one to five R33, poly(ethylene glycol), methoxypoly(ethylene glycol), pyrrolidinyl and piperidinyl; or the C1-30 alkyl is substituted with at least one -OR31, wherein R31 is poly(ethylene glycol) or methoxypoly(ethylene glycol); R28a is selected from C1-30 alkyl substituted with one to five R25, C1-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly (ethylene glycol), and methoxypoly (ethylene glycol); (4) R1 is -NR3R4, and R4 is selected from C1-30 alkyl substituted with one to five R20, Ci-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), methoxypoly(ethylene glycol), and -NR13R14; wherein the Ci-30 alkyl is substituted with at least one R20 selected from halo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -S(0)o-2R28, -NHS(0)o-2R28, -S(0)o-2NHR28, -NHS(O)0 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, NHC(O)OR28, -OC(O)N(R28)2, C3-10 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, and heteroaryl optionally substituted with one to five R26; or (5) R6 is selected from C1-6 alkyl substituted with one to five R29, -OR17, -S(0)o 2R16, C(O)OR15, -OC(O)R16, -NO2, -NR15R15, -C(O)NR15R15, -S(O)0-2NHR16, -NHS(O)0-2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol), wherein R17 is selected from C1-30 alkyl substituted with one to five R27, C1-30 heteroalkyl optionally substituted with one to five R27, C310 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol).

[0197] Provided herein is a compound of Formula (I): R8                                (I), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein R1 is selected from -NR3R4, heterocyclyl optionally substituted with one to five R20, and heteroaryl optionally substituted with one to five R21; R2 is selected from C2-30 alkyl optionally substituted with one to five R19, C1-30 heteroalkyl optionally substituted with one to five R19, -NO2, -OR18, -S(0)o-2R18, and -NRnR18, wherein R18 is selected from Ci-3ohaloalkyl, C2 30 alkyl optionally substituted with one to five R19 and C2 30 heteroalkyl optionally substituted with one to five R19; wherein when R2 is ethyl, then R6 is not methyl or methoxy; R3 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21; R4 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), methoxypoly(ethylene glycol), and -NR13R14; R5, R7 and R8 are each independently selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, Ci-3o heteroalkyl optionally substituted with one to five R29, -OR15, -S(0)o-2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, and -C(O)NR15R15; R6 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, C1-30 heteroalkyl optionally substituted with one to five R29, -OR17, -S(0)o 2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, -C(O)NR15R15, -NR15C(O)R16, -S(0)o-2NR15R15, -NR15S(0)o-2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol), or R6 and R7 together with atoms to which they are attached form C510 cycloalkyl optionally substituted with one to five R29, heterocyclyl optionally substituted with one to five R29, aryl optionally substituted with one to five R30, or heteroaryl optionally substituted with one to five R30; R9 is independently selected from halo, Ci s alkyl optionally substituted with one to five R22, -OH, -OR10, -CN, and -NRnR12; n is 0, 1, 2, 3 or 4; R10 is independently selected from Cno alkyl optionally substituted with one to five R22, and C310 cycloalkyl optionally substituted with one to five R22; R11 and R12 are each independently H or C1-6 alkyl optionally substituted with one to five R22; R13 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21; R14 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R15 is independently selected from H, C1-30 alkyl optionally substituted with one to five R23, Ci-30 heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R16 is selected from C1-30 alkyl optionally substituted with one to five R23, C1-30heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R17 is selected from H, C1-30 alkyl optionally substituted with one to five R27, C1-30 heteroalkyl optionally substituted with one to five R27, C310 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R18 is selected from C1-30 alkyl optionally substituted with one to five R19 and C1-30 heteroalkyl optionally substituted with one to five R19; each R20 is independently selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(0)o-2R28, -NHS(0)o 2R28, -S(0)o-2NHR28, -NHS(0)o 2NHR28, -C(O)NH2, -C(O)NHR28, -C(O)N(R28)2, -NHC(O)R28, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, c1-30 alkyl optionally substituted with one to five R25, C1-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R21 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(O)0-2R28, -NHS(0)o-2R28, -S(O)0-2NHR28, -NHS(O)0 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, C1-6 alkyl optionally substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R19 or R22 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl, C1-4 haloalkyl, C1-4 hydroxyalkyl, Cm alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o.2-Ci4 alkyl, -NHS(0)o-2-Cm alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-C14 alkyl, -C(O)NH-C 1-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4 haloalkyl, -N(Ci-4 haloalkyl)2, -C(O)-Ci4 haloalkyl, -S(0)o2-Ci-4 haloalkyl, -NHS(0)o 2-C1-4 haloalkyl, -S(0)o 2NH-C14 haloalkyl, -NHS(0)o-2NH-Ci-4 haloalkyl, -C(O)NH-Ci-4 haloalkyl, -NHC(O)-Ci-4 haloalkyl, -C(0)N(Cm haloalkyl)2, -OC(O)NH-Ci-4 haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci-4haloalkyl)2, and C310 cycloalkyl; each R25 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, c1-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R26 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(O)0-2R31, -NR32S(O)0-2R31, -S(O)0-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R31 is independently selected C1-30 alkyl optionally substituted with one to five R33, Ci-30 heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol) and methoxypoly(ethylene glycol); each R32 is independently selected H and C1-4 alkyl; each R23, R27, R29 or R33 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl optionally substituted with phenyl, Ci-4 haloalkyl, C1-4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-Ci-4 alkyl, -NHS(0)o-2-Ci-4 alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o-2NH-Ci-4 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4alkyl)2, -NH-Ci 4haloalkyl, -N(Ci-4haloalkyl)2, -C(O)-Ci-4haloalkyl, -S(0)o-2-C1-4 haloalkyl, -NHS(0)o-2-Cm haloalkyl, -S(0)o-2NH-Cm haloalkyl, -NHS(0)o 2NH-C1 4 haloalkyl, -C(O)NH-Ci-4 haloalkyl, -NHC(O)-Ci-4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-Ci 4 haloalkyl, -NHC(O)O-Ci 4 haloalkyl, -0C(0)N(Cm haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o 4-O-poly(ethylene glycol), methoxypoly(ethylene glycol)-0-(CH2)o4-, and sugar moiety; each R24, R30 or R34 is independently selected from halo, -NH2, -OH, -CN, -NO2, C1-4 alkyl, C1-4 haloalkyl, C1-4 hydroxyalkyl, Cj4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)OH, -C(O)O-Ci-4 alkyl, -S(0)o-2-Ci-4 alkyl, -NHS(0)o-2-Cm alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-C14 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4haloalkyl, -N(Ci-4 haloalkyl)2, -C(O)-Ci4 haloalkyl, -S(0)o2-Ci-4 haloalkyl, -NHS(0)o 2-C1-4 haloalkyl, -S(0)o 2NH-C14 haloalkyl, -NHS(0)o-2NH-Cm haloalkyl, -C(O)NH-Ci-4 haloalkyl, -NHC(O)-Ci- 4 haloalkyl, -C(0)N(Cm haloalkyl)2, -OC(O)NH-Ci-4 haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci-4haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl, heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o 4-O-poly(ethylene glycol); -(CH2)o 4-O-methoxypoly(ethylene glycol) and sugar moiety; and each R28 is independently selected from C1-30 alkyl optionally substituted with one to five R25, Ci-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly (ethylene glycol), and methoxypoly(ethylene glycol).

[0198] Provided herein is a compound of Formula (I): R8                                (I), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein R1 is heteroaryl optionally substituted with one to five R21, or fused heterocyclyl optionally substituted with one to five R20; or R1 is heterocyclyl substituted with at least one R20 selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28a, -NHS(O)0-2R28, -OC(O)R28, -S(0)o-2R28, -S(0)o-2NHR28, -NHS(0)o 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, c1-30 alkyl substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, heterocyclyl substituted with one to five R25, poly(ethylene glycol), and methoxypoly(ethylene glycol); wherein at least one R25 is selected from halo, -NH2, -OH, -CN, -NO2, oxo, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, heterocyclyl substituted with one to five R33, poly(ethylene glycol), methoxypoly(ethylene glycol), pyrrolidinyl and piperidinyl; or the C1-30 alkyl is substituted with at least one -OR31a, wherein R31a is poly(ethylene glycol) or methoxypoly(ethylene glycol); and R28a is selected from Ci-30 alkyl substituted with one to five R25, C1-30 heteroalkyl optionally substituted with one to five R25, C3-10 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); or R1 is -NR3R4, R2 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R19, C1-30 heteroalkyl optionally substituted with one to five R19, -OH, -OR18, -CN, -NO2, -NH2, -S(0)o-2R18, and -NRnR18; R3 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21, and R4 is selected from C1-30 alkyl substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), methoxypoly(ethylene glycol), and -NR13R14, wherein the Ci-30 alkyl is substituted with at least one R20 selected from halo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -S(0)o-2R28, -NHS(0)o-2R28, -S(0)o-2NHR28, -NHS(O)0 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, C3-10 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, and heteroaryl optionally substituted with one to five R26; R5, R7 and R8 are each independently selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, Ci-3o heteroalkyl optionally substituted with one to five R29, -OR15, -S(0)o 2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, and -C(O)NR15R15; R6 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, C1-30 heteroalkyl optionally substituted with one to five R29, -OR17, -S(0)o 2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, -C(O)NR15R15, -NR15C(O)R16, -S(0)o-2NR15R15, -NR15S(0)o-2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), methoxypoly(ethylene glycol), and sugar moiety, or R6 and R7 together with atoms to which they are attached form C510 cycloalkyl optionally substituted with one to five R29, heterocyclyl optionally substituted with one to five R29, aryl optionally substituted with one to five R30, or heteroaryl optionally substituted with one to five R30; R9 is independently selected from halo, Ci s alkyl optionally substituted with one to five R22, -OH, -OR10, -CN, and -NRnR12; n is 0, 1, 2, 3 or 4; R10 is independently selected from Cno alkyl optionally substituted with one to five R22, and C310 cycloalkyl optionally substituted with one to five R22; R11 and R12 are each independently H or C1-6 alkyl optionally substituted with one to five R22; R13 is selected from H, Ci-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21; R14 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R15 is independently selected from H, C1-30 alkyl optionally substituted with one to five R23, Ci-30 heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, and heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), methoxypoly(ethylene glycol); R16 is selected from C1-30 alkyl optionally substituted with one to five R23, C1-30heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R17 is selected from H, C1-30 alkyl optionally substituted with one to five R27, C1-30 heteroalkyl optionally substituted with one to five R27, C310 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R18 is selected from C1-30 alkyl optionally substituted with one to five R19 and C1-30 heteroalkyl optionally substituted with one to five R19; each R20 is independently selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(0)o-2R28, -NHS(0)o 2R28, -S(0)o-2NHR28, -NHS(0)o 2NHR28, -C(O)NH2, -C(O)NHR28, -C(O)N(R28)2, -NHC(O)R28, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, c1-30 alkyl optionally substituted with one to five R25, C1-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R21 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(O)0-2R28, -NHS(O)0-2R28, -S(O)0-2NHR28, -NHS(O)0 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, C1-6 alkyl optionally substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R19 or R22 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl, C1-4 haloalkyl, C1-4 hydroxyalkyl, Cm alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o.2-Ci4 alkyl, -NHS(0)o-2-Cm alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-C14 alkyl, -C(0)NH-Cm alkyl, -NHC(O)-Ci-4 alkyl, -C(0)N(Cm alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4 haloalkyl, -N(Ci-4 haloalkyl)2, -C(O)-Ci4 haloalkyl, -S(0)o 2-Ci-4 haloalkyl, -NHS(0)o 2-C1-4 haloalkyl, -S(0)o 2NH-C14 haloalkyl, -NHS(0)o-2NH-Cm haloalkyl, -C(O)NH-Ci-4 haloalkyl, -NHC(O)-Ci-4 haloalkyl, -C(0)N(Cm haloalkyl)2, -OC(O)NH-Ci-4 haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci-4haloalkyl)2, and C310 cycloalkyl; each R25 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R26 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(O)0-2R31, -NR32S(O)0-2R31, -S(O)0-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R31 is independently selected C1-30 alkyl optionally substituted with one to five R33, Ci-30 heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol) and methoxypoly(ethylene glycol); each R32 is independently selected H and C1-4 alkyl; each R23, R27, R29 or R33 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl optionally substituted with phenyl, Ci-4 haloalkyl, C1-4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-Ci-4 alkyl, -NHS(0)o-2-Ci-4 alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o-2NH-Ci-4 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4alkyl)2, -NH-Ci 4haloalkyl, -N(Ci-4haloalkyl)2, -C(O)-Ci-4haloalkyl, -S(0)o-2-C1-4 haloalkyl, -NHS(0)o-2-Cm haloalkyl, -S(0)o-2NH-Cm haloalkyl, -NHS(0)o 2NH-C1 4 haloalkyl, -C(O)NH-Ci-4 haloalkyl, -NHC(O)-Ci-4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-Ci 4 haloalkyl, -NHC(O)O-Ci 4 haloalkyl, -0C(0)N(Cm haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o 4-O-poly(ethylene glycol), methoxypoly(ethylene glycol)-0-(CH2)o4-, and sugar moiety; each R24, R30 or R34 is independently selected from halo, -NH2, -OH, -CN, -NO2, C1-4 alkyl, C1-4 hydroxyalkyl, C1-4 haloalkyl, Cj4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)OH, -C(O)O-Ci-4 alkyl, -S(0)o-2-Ci-4 alkyl, -NHS(0)o-2-Cm alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-C14 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4haloalkyl, -N(Ci-4 haloalkyl)2, -C(O)-Ci4 haloalkyl, -S(0)o 2-Ci-4 haloalkyl, -NHS(0)o 2-C1-4 haloalkyl, -S(0)o 2NH-C14 haloalkyl, -NHS(0)o-2NH-Cm haloalkyl, -C(O)NH-Ci-4 haloalkyl, -NHC(O)-Ci- 4 haloalkyl, -C(0)N(Cm haloalkyl)2, -OC(O)NH-Ci-4 haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci-4haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl, heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o 4-O-poly(ethylene glycol), -(CH2)o 4-O-methoxypoly(ethylene glycol) and sugar moiety; and each R28 is independently selected from C1-30 alkyl optionally substituted with one to five R25, Ci-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly (ethylene glycol), and methoxypoly(ethylene glycol).

[0199] Provided herein is a compound of Formula (I): R8                                (I), or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein R1 is selected from -NR3R4, heterocyclyl optionally substituted with one to five R20, and heteroaryl optionally substituted with one to five R21; R2 is selected from H, halo, C1-30 alkyl optionally substituted with one to five R19, C1-30 heteroalkyl optionally substituted with one to five R19, -OH, -OR18, -CN, -NO2, -NH2, -S(0)o-2R18, and -NRnR18; R3 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21, R4 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), methoxypoly(ethylene glycol), and -NR13R14; R5, R7 and R8 are each independently selected from H, halo, C1-30 alkyl optionally substituted with one to five R29, Ci-3o heteroalkyl optionally substituted with one to five R29, -OR15, -S(0)o-2R16, -C(O)OR15, -OC(O)R16, -CN, -NO2, -NR15R15, and -C(O)NR15R15; R6 is selected from C1-6 alkyl substituted with one to five R29, -OR17, -S(0)o 2R16, C(O)OR15, -OC(O)R16, -NO2, -NR15R15, -C(O)NR15R15, -S(0)o-2NHR16, -NHS(0)o 2R16, heterocyclyl optionally substituted with one to five R29, heteroaryl optionally substituted with one to five R30, poly(ethylene glycol), and methoxypoly(ethylene glycol), wherein R17 is selected from Ci-30 alkyl substituted with one to five R27, C1-30 heteroalkyl optionally substituted with one to five R27, C3-10 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R9 is independently selected from halo, Ci s alkyl optionally substituted with one to five R22, -OH, -OR10, -CN, and -NRnR12; n is 0, 1, 2, 3 or 4; R10 is independently selected from Cno alkyl optionally substituted with one to five R22, and C3 io cycloalkyl optionally substituted with one to five R22; R11 and R12 are each independently H or C1-6 alkyl optionally substituted with one to five R22; R13 is selected from H, C1-6 alkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, and heteroaryl optionally substituted with one to five R21; R14 is selected from H, C1-30 alkyl optionally substituted with one to five R20, C1-30 heteroalkyl optionally substituted with one to five R20, C310 cycloalkyl optionally substituted with one to five R20, heterocyclyl optionally substituted with one to five R20, aryl optionally substituted with one to five R21, heteroaryl optionally substituted with one to five R21, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R15 is independently selected from H, C1-30 alkyl optionally substituted with one to five R23, Ci-30 heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R16 is selected from C1-30 alkyl optionally substituted with one to five R23, C1-30heteroalkyl optionally substituted with one to five R23, C310 cycloalkyl optionally substituted with one to five R23, heterocyclyl optionally substituted with one to five R23, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R17 is selected from H, C1-30 alkyl optionally substituted with one to five R27, C1-30 heteroalkyl optionally substituted with one to five R27, C310 cycloalkyl optionally substituted with one to five R27, heterocyclyl optionally substituted with one to five R27, aryl optionally substituted with one to five R24, heteroaryl optionally substituted with one to five R24, poly(ethylene glycol), and methoxypoly(ethylene glycol); R18 is selected from C1-30 alkyl optionally substituted with one to five R19 and C1-30 heteroalkyl optionally substituted with one to five R19; each R20 is independently selected from halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(0)o-2R28, -NHS(0)o 2R28, -S(0)o-2NHR28, -NHS(0)o 2NHR28, -C(O)NH2, -C(O)NHR28, -C(O)N(R28)2, -NHC(O)R28, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, c1-30 alkyl optionally substituted with one to five R25, C1-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R21 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(O)0-2R28, -NHS(O)0-2R28, -S(O)0-2NHR28, -NHS(O)0 2NHR28, -C(O)NHR28, -NHC(O)R28, -C(O)N(R28)2, -OC(O)NHR28, -NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, C1-6 alkyl optionally substituted with one to five R25, C1-30heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R22 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl, C1-4 haloalkyl, C1-4hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci 4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-Ci-4 alkyl, -NHS(O)0-2-Ci-4 alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-Ci 4 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4 haloalkyl, -N(Ci-4 haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(0)o 2-Ci-4 haloalkyl, -NHS(0)o 2-Ci-4 haloalkyl, -S(0)o 2NH-Ci 4 haloalkyl, -NHS(O)0-2NH-Ci-4 haloalkyl, -C(O)NH-Ci-4haloalkyl, -NHC(O)-Ci-4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-Ci-4haloalkyl, -NHC(O)O-Ci-4haloalkyl, -OC(O)N(Ci-4haloalkyl)2, and C310 cycloalkyl; each R25 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R26 is independently selected from halo, -NH2, -OH, -CN, -NO2, -OR31, -NHR31, -N(R31)2, -C(O)R31, -C(O)OR31, -C(O)OH, -S(0)o-2R31, -NR32S(0)o-2R31, -S(0)o-2NR32R31, -NR32S(0)o-2NR32R31, -C(O)NH2, -C(O)NHR31, -NR32C(O)R31, -C(O)N(R31)2, -OC(O)NHR31, -NR32C(O)OR31, -OC(O)N(R31)2, -NR32C(O)NH2, -NR32C(O)NHR31, -NR32C(O)N(R31)2, Ci-30 alkyl optionally substituted with one to five R33, C1-30heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol), and methoxypoly(ethylene glycol); each R31 is independently selected C1-30 alkyl optionally substituted with one to five R33, Ci-30 heteroalkyl optionally substituted with one to five R33, C310 cycloalkyl optionally substituted with one to five R33, heterocyclyl optionally substituted with one to five R33, aryl optionally substituted with one to five R34, heteroaryl optionally substituted with one to five R34, poly(ethylene glycol) and methoxypoly(ethylene glycol); each R32 is independently selected H and C1-4 alkyl; each R23, R27, R29 or R33 is independently selected from halo, -NH2, -OH, -CN, -NO2, oxo, C1-4 alkyl optionally substituted with phenyl, Ci-4 haloalkyl, C1-4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci-4 alkyl, -C(O)O-Ci-4 alkyl, -C(O)OH, -S(0)o-2-Ci-4 alkyl, -NHS(0)o-2-Ci-4 alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o-2NH-Cm alkyl, -C(O)NH-Ci-4 alkyl, -NHC(0)-Cm alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-Cm haloalkyl, -N(CM haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(0)o-2-Ci-4 haloalkyl, -NHS(0)o-2-Ci-4 haloalkyl, -S(0)o-2NH-Ci-4haloalkyl, -NHS(0)o2NH-Ci-4 haloalkyl, -C(O)NH-Ci-4 haloalkyl, -NHC(O)-Ci-4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -0C(0)NH-Cm haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci 4 haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl heteroaryl, (CH2)i 30-C(O)OH, -(CH2)o-4-0-poly(ethylene glycol), methoxypoly(ethylene glycol)-0-(CH2)o-4-, and sugar moiety; each R24, R30 or R34 is independently selected from halo, -NH2, -OH, -CN, -NO2, C1-4 alkyl, Ci-4 haloalkyl, Cj4 hydroxyalkyl, C1-4 alkoxy, -NH-Ci 4 alkyl, -N(Ci-4 alkyl)2, -C(O)-Ci 4 alkyl, -C(O)OH, -C(O)O-Ci-4 alkyl, -S(0)o-2-CM alkyl, -NHS(0)o-2-Cm alkyl, -S(0)o-2NH-Ci-4 alkyl, -NHS(0)o 2NH-Ci 4 alkyl, -C(O)NH-Ci-4 alkyl, -NHC(O)-Ci-4 alkyl, -C(O)N(Ci-4 alkyl)2, -OC(O)NH-Ci-4 alkyl, -NHC(O)O-Ci-4 alkyl, -OC(O)N(Ci-4 alkyl)2, -NH-C1-4 haloalkyl, -N(Ci-4haloalkyl)2, -C(O)-Ci-4 haloalkyl, -S(0)o-2-Ci-4 haloalkyl, -NHS(0)o-2-Cm haloalkyl, -S(0)o-2NH-Ci-4haloalkyl, -NHS(0)o 2NH-Ci 4 haloalkyl, -C(O)NH-Ci 4 haloalkyl, -NHC(O)-Ci 4 haloalkyl, -C(O)N(Ci-4haloalkyl)2, -OC(O)NH-Ci 4 haloalkyl, -NHC(O)O-Ci-4 haloalkyl, -OC(O)N(Ci-4haloalkyl)2, C310 cycloalkyl, heterocyclyl, aryl, heteroaryl, -(CH2)i 30-C(O)OH, -(CH2)o-4-0-poly(ethylene glycol), -(CH2)o-4-0-methoxypoly(ethylene glycol) and sugar moiety; and each R28 is independently selected from C1-30 alkyl optionally substituted with one to five R25, Ci-30 heteroalkyl optionally substituted with one to five R25, C310 cycloalkyl optionally substituted with one to five R25, heterocyclyl optionally substituted with one to five R25, aryl optionally substituted with one to five R26, heteroaryl optionally substituted with one to five R26, poly (ethylene glycol), and methoxypoly(ethylene glycol).

[0200] “Poly(ethylene glycol) refers to a poly ether compound of general formula ,0. / x H Hd Fo n , where n varies from 2 to 500,000. In certain embodiments, poly(ethylene glycol) has an average molecular weight of less than 20,000. In certain embodiments, poly(ethylene glycol) has an average molecular weight of less than 15,000. In certain embodiments, poly(ethylene glycol) has an average molecular weight of less than 10,000. In certain embodiments, poly(ethylene glycol) has an average molecular weight of less than 5,000. In certain embodiments, poly(ethylene glycol) has an average molecular weight of less than 2,000. In certain embodiments, poly(ethylene glycol) has an average molecular weight of about 20,000 to about 2,000. In certain embodiments, poly(ethylene glycol) has an average molecular weight of about 10,000 to about 2,000.

[0201] “Methoxypoly(ethylene glycol) refers to a polyether compound of general formula h3c< ro^ , where n varies from 2 to 500,000. In certain embodiments, methoxypoly(ethylene glycol) has an average molecular weight of less than 20,000. In certain embodiments, methoxypoly(ethylene glycol) has an average molecular weight of less than 15,000. In certain embodiments, methoxypoly(ethylene glycol) has an average molecular weight of less than 15,000. In certain embodiments, methoxypoly(ethylene glycol) has an average molecular weight of less than 10,000. In certain embodiments, methoxypoly(ethylene glycol) has an average molecular weight of less than 5,000. In certain embodiments, methoxypoly(ethylene glycol) has an average molecular weight of less than 2,000. In certain embodiments, methoxypoly(ethylene glycol) has an average molecular weight of about 20,000 to about 2,000. In certain embodiments, methoxypoly(ethylene glycol) has an average molecular weight of about 10,000 to about 2,000.

[0202] In some embodiments, provided is a compound of Formula (XII): or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein: N R1 is optionally substituted each of s, t, u, v, p and q is independently 0, 1,2, or 3, provided that the sum of s and t is 1, 2, 3 or 4, the sum of u and v is 1, 2, 3 or 4, and the sum of p and q is 1, 2, 3 or 4; y is 0 or 1; z is 0 or 1; provided that y and z are not both 0; Z1 is C or N; when Z1 is C, R20a is H, halo, hydroxy, alkyl, or hydroxyalkyl; when Z1 is N, R20a is absent; Z2 is CH or N; Z3 is C or N; when Z3 is C, R20b is H, halo, hydroxy, alkyl, or hydroxyalkyl; when Z3 is N, R20b is absent; Z4 is CH or N; Z5 is CH2, CHR25, CR25R25, C(=O), NR25, O, or S(O)0 2; each R25 is independently H, halo, alkyl or hydroxyalkyl; R211 is C2-4o alkyl, C2-4o alkenyl, or C2-4oalkynyl; R6 is H, halo, alkyl, haloalkyl, hydroxy, alkoxy, haloalkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, amido, sulfinamido, or sulfonamido; and R91 and R92 are independently selected from H and halo.

[0203] In some embodiments, provided is a pharmaceutical composition comprising a compound of Formula (XII): (XII) or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof; wherein: R1 is                 ; each of s, t, u, v, p and q is independently 0, 1,2, or 3, provided that the sum of s and t is 1, 2, 3 or 4, the sum of u and v is 1, 2, 3 or 4, and the sum of p and q is 1, 2, 3 or 4; y is 0 or 1; z is 0 or 1; provided that y and z are not both 0; Z1 is CH or N; Z2 is CH or N; Z3 is CH or N; Z4 is CH or N; Z5 is CH2, CHR25, CR25R25, C(=O), NR25, O, or S(0)o-2; each R25 is independently H, halo, alkyl or hydroxyalkyl; R211 is C2-4o alkyl, C2-4o alkenyl, or C2-4o alkynyl; R6 is H, halo, alkyl, haloalkyl, hydroxy, alkoxy, haloalkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, amido, sulfinamido, or sulfonamido; and R91 and R92 are independently selected from H and halo.

[0204] In some embodiments, in the compound of Formula (XII), R211 is C5-40 alkyl, C5 40 alkenyl, or C5 40 alkynyl. In some embodiments, in the compound of Formula (XII), R211 is C10-40 alkyl, C10-40 alkenyl, or C10-40 alkynyl. In some embodiments, in the compound of Formula (XII), R211 is C10-25 alkyl, C10 25 alkenyl, or C10 25 alkynyl. In some embodiments, in the compound of Formula (XII), R211 is C5 40 alkyl. In some embodiments, in the compound of Formula (XII), R211 is C10 40 alkyl. In some embodiments, in the compound of Formula (XII), R211 is C10 30 alkyl. In some embodiments, in the compound of Formula (XII), R211 is Cio 2s alkyl.

[0205] In some embodiments, in the compound of Formula (XII), R91 and R92 are independently selected from H and F. In some embodiments, in the compound of Formula (XII), R91 is H and R92 is F. In some embodiments, in the compound of Formula (XII), R91 is F and R92 is H. In some embodiments, in the compound of Formula (XII), R91 and R92 are both H. In some embodiments, in the compound of Formula (XII), R91 and R92 are both F.

[0206] In some embodiments, in the compound of Formula (XII), R6 is hydroxy, alkoxy, haloalkoxy, alkylthio, sulfoxido, or sulfonyl. In some embodiments, in the compound of Formula (XII), R6is hydroxy, or alkoxy. In some embodiments, in the compound of Formula (XII), R6is alkylthio, sulfoxido, or sulfonyl. In some embodiments, in the compound of Formula (XII), R6is sulfonyl. In some embodiments, in the compound of Formula (XII), R6is sulfoxido. In some embodiments, in the compound of Formula (XII), R6is methylsulfoxido.

[0207] In some embodiments, in the compound of Formula (XII), each ring in R1 is independently and optionally further substituted with halo, hydroxy, alkyl, hydroxyalkyl, or oxo. In some Z5 I ^R20a _Zf^ N embodiments, in the compound of Formula (XII), R1 is , wherein Z1, Z4, Z5, s, t, p, q and R20a are as defined herein, and each ring in R1 is independently and optionally further substituted with halo, hydroxy, alkyl, hydroxyalkyl, or oxo. In some embodiments, in the compound of Z5 ^z4 I R20b Z3 I ^R20a _Z1^ N Formula (XII), R1 is               , wherein Z1, Z2, Z3, Z4, Z5, s, t, u, v, p, q, R20a and R20b, are as defined herein, and each ring in R1 is independently and optionally further substituted with halo, hydroxy, alkyl, hydroxyalkyl, or oxo. In some embodiments, in the compound of Formula (XII), R1 is , wherein Z'is CH or N, and Z4, Z5, s, t, p, q are as defined herein. In some embodiments, in the compound of Formula (XII), R1 is         , wherein Z1 is CH or N, Z3is CH or N, and Z2, Z4, Z5, s, t, u, v, p, q are as defined herein.

[0209] In some embodiments, in the compound of Formula (XII), R1 is selected from

[0210] In some embodiments, the compound of Formula (XII) is selected from 395 461 465 466 530 542 or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof.

[0211] In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a salt selected from mono, bis, or tris succinate, oxalate, citrate, maleate, adipate, or fumarate salts thereof. In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a hydrate of a mono, bis or tris succinate, oxalate, citrate, maleate, adipate, or fumarate salt thereof, e.g., a salt of formula

[0212] In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a mono, bis, or tris succinate salt. In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a tris succinate salt. In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a tris succinate salt prepared from succinic acid dihydrate.

[0213] In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a mono, bis, or tris oxalate salt. In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a tris oxalate salt. In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a tris oxalate salt prepared from oxalic acid dihydrate.

[0214] In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a mono, bis, or tris adipate salt. In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a tris adipate salt. In some embodiments, any compound of Formula (I) or sub-formulae thereof, is a tris adipate salt prepared from adipic acid dihydrate.

[0215] In certain embodiments, provided is a compound selected from Table 1, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof. Table 1 Ex. Structure Name 1 6 1 ox / o Y Y Y Y Y 3-((4-ethylphenyl)sulfonyl)-4-(4-methylpiperazin-1 -yl)-6-(trifluoromethoxy)quinoline 2 n O F 3-((4-ethylphenyl)sulfonyl)-4-(piperidin-l-yl)-6-(trifluoromethoxy)quinoline 3 0 1 <\zo F / O^^YJY^. Y Y Y Y Y 4-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)morpholine 4 6 7 °\ / ° FsCO^^^Jx'M'^x Y Y Y Y Y 3-((4-ethylphenyl)sulfonyl)-4-(4-methylpiperidin-1 -yl)-6-(trifluoromethoxy)quinoline 5 HO'Y 0 1 ox / o FsCOx^^ / Y / S Y Y Y Y T 2-(4-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperazin-1 -yl)ethan-1 -ol 6 7 °\ / ° FaCOx^^Y^YY'^ Y Y Y Y 1 3-((4-ethylphenyl)sulfonyl)-4-(4-ethylpiperazin-1 -yl) -6 -(trifluoromethoxy)quinoline Ex. Structure Name 7 J A O o u LL° 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl) -6 - (trifluoromethoxy)quinoline 8 6 7 °\ / ° XT J X A l-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol 9 0 7 °\z° x t j ta ethyl 4-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4- yl)piperazine-1 -carboxylate 10 0 1 O' / O ■'xiytu 3-((4-ethylphenyl)sulfonyl)-4-(4-(4-fluorophenyl)piperazin-1 - y 1) - 6 -(trifluoromethoxy)quinoline 11 0 7 0. .0 TA J TA 4-([l,4'-bipiperidin]-l'-yl)-3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinoline Ex. Structure Name 12 Q L-OH 7 °x / ° Y Y Y Y JJ l-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-4-phenylpiperidin-4-ol 13 Q 7 °\ / ° f3co\-^^YYs Y Y Y Y JJ 3-((4-ethylphenyl)sulfonyl)-4-(4-phenylpiperazin-1 -yl) -6 -(trifluoromethoxy)quinoline 14 Q. Y Y Y Y ? 3-((4-ethylphenyl)sulfonyl)-4-(pyrrolidin-l-yl)-6-(trifluoromethoxy)quinoline 15 O 2    / )-2   )— o / / \ / 1' l-(3-((4-ethylphenyl)sulfonyl)-6- methoxyquinolin-4-yl)piperidin-4-ol 16 7 °\ / ° H 3CO^^XJS Y Y Y Y ethyl 4-(3-((4-ethylphenyl)sulfonyl)-6-methoxyquinolin-4-yl)piperazine-1 -carboxylate Ex. Structure Name 17 F c 7 °x / ° Y Y Y Y JI 3-((4-ethylphenyl)sulfonyl)-4-(4-(4-fluorophenyl)piperazin-1 -yl) -6 -methoxyquinoline 18 ^\Hox / o Y Y Y Y JJ N-cyclohexyl-3-((4-ethylphenyl)sulfonyl)-6-methoxyquinolin-4-amine 19 J d^\ LL-           O m X 3-((4-ethylphenyl)sulfonyl)-N-(4-fluorophenyl)-6-methoxyquinolin-4-amine 20 1 0 7 °\z° Y Y Y Y JL 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4- (4-methylpiperazin-1 -yl)quinoline 21 0 7 °\ / ° HC0^^X;sV^ Y Y Y Y Y 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4-(piperidin-1 -yl)quinoline 22 X UJ O vy- C3° x° - 4-(3-((4-ethylphenyl)sulfonyl)-6-methoxyquinolin-4-yl)morpholine Ex. Structure Name 23 7 0. 0 Y Y Y Y Ji 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4- (4-methylpiperidin-1 -yl)quinoline 24 0 7 °\ / ° Y Y Y Y 1 3-((4-ethylphenyl)sulfonyl)-4-(4-ethylpiperazin-1 -yl)-6-methoxy quinoline 25 ? °x / ° Y Y Y Y 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4-(pyrrolidin-1 -yl)quinoline 26 Y tQ^ry^-y o m X 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4- (4-phenylpiperazin-1 -yl)quinoline 27 7 Y H3C0^^Y^YSY^s Y Y J Y JL 4-([l,4'-bipiperidin]-l'-yl)-3-((4-ethylphenyl)sulfonyl)-6-methoxyquinoline 28 0 JL°h 7 °\z° H3C0^^Y^YSY^s Y Y J Y JL l-(3-((4-ethylphenyl)sulfonyl)-6-methoxyquinolin-4-yl)-4-phenylpiperidin-4-ol Ex. Structure Name 29 Q. Y Y Y TO 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4-(4-methyl-1,4-diazepan-1 -yl)quinoline 30 0 7 °\ / ° Y Y Y Y 1 3-((4-ethylphenyl)sulfonyl)-4-(4-isopropylpiperazin-1 -yl)-6-methoxyquinoline 31 OXZO Y Y Y Y JL 4-(azepan-l-yl)-3-((4-ethylphenyl)sulfonyl)-6-methoxyquinoline 32 Z  \—Z   Z / / \___ / —\ zo '— 3-((4-ethylphenyl)sulfonyl)-6-methyl-4- (4-methylpiperazin-1 -yl)quinoline 33 °x^— / —\ /   z—r   z 3-((4-ethylphenyl)sulfonyl)-6-methyl-4-(4-methyl-1,4-diazepan-1 -yl)quinoline 34 6 ? °K / ° Y Y Y Y J. l-(3-((4-ethylphenyl)sulfonyl)-6- methylquinolin-4-yl)piperidin-4-ol Ex. Structure Name 35 / / \ / \__ / / xo 4-([l,4'-bipiperidin]-l’-yl)-3-((4- ethylphenyl)sulfonyl)-6-methylquinoline 36 D O IT J TO XX / 3-((4-ethylphenyl)sulfonyl)-6-methyl-4-(piperidin-1 -yl)quinoline 37 / \ —2 2—\ 3-((4-ethylphenyl)sulfonyl)-6-fluoro-4-(4-methylpiperazin-1 -yl)quinoline 38 \—\ 7 °\ / ° IT T TX 3-((4-ethylphenyl)sulfonyl)-6-fluoro-4-(4-methyl-1,4-diazepan-1 -yl)quinoline 39 OH 6 7 o o ¥ T J T 1 l-(3-((4-ethylphenyl)sulfonyl)-6- fluoroquinolin-4-yl)piperidin-4-ol Ex. Structure Name 40 0 T T Y Y X XXNZ  vV / 4-([l,4'-bipiperidin]-l'-yl)-3-((4- ethylphenyl)sulfonyl)-6-fluoroquinoline 41 D O FvxxJYx Y Y Y Y Y XXZ XX / 3-((4-ethylphenyl)sulfonyl)-6-fluoro-4-(piperidin-1 -yl)quinoline 42 0. /    N- \ H0     /     1 7 0. 0 Y Y Y Y Y 2-(4-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-l,4-diazepan-l-yl) acetic acid 43 0 !C0\ / / XX / / Y JJ Y Y Y 4-([l,4'-bipiperidin]-l'-yl)-3-((4-methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinoline 44 OH FsCO^^Y^YY'^s Y Y Y Y Y l-(3-((4-methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol Ex. Structure Name 45 CN 7 0. 0 T Y Y Y JL 4-(4-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4- yl)piperazin-1 -yl)benzonitrile 46 J o o LL. 3-((4-ethylphenyl)sulfonyl)-4-(4-(pyrrolidin-1 -yl)piperidin-1 -yl) -6 -(trifluoromethoxy)quinoline 47 0x o , 6. Y Y Y Y JJ ethyl l-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidine-4-carboxylate 48 Y1 n O O „ 5 ZW zvV '--\ zo '--- t / \ (l-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-yl)methanol 49 o 7 °x / ° Y Y Y Y JI N-benzyl-3-((4-ethylphenyl)sulfonyl)-N-methyl-6-(trifluoromethoxy)quinolin-4-amine Ex. Structure Name 50 L ^N. iHox / o Y T Y Y Y 3-((4-ethylphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (trifluoromethoxy)quinolin-4-amine 51 < N ? °\ / ° wu 3-((4-ethylphenyl)sulfonyl)-4-(lH-l,2,4-triazol-l-yl)-6- (trifluoromethoxy)quinoline 52 oYb ? °\ / ° Y Y Y Y Y 8-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-l,4- dioxa- 8 - azaspiro [4.5 ] dec ane 53 °y0H r / 'o^^Yvr^ Y Y Y Y Y l-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidine-4-carboxylic acid 54 c f3co^^Y^YsY^^ y Y J 11 —^CN 4-((4-( [l,4'-bipiperidin]-l'-yl)-6-(trifluoromethoxy)quinolin-3-yl)sulfonyl)benzonitrile 55 0 0 NfXTQ. 2-(4-([ 1,4'-bipiperidin] -l'-yl)-3-((4-ethylphenyl)sulfonyl)quinolin-6-yl) acetonitrile Ex. Structure Name 56 0 Y Y Y Y Y 4-( [ 1,4'-bipiperidin] -1 '-yl)-3-((3,4-dimethoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinoline 57 o V o 3-((3,4-dimethoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)-6- (trifluoromethoxy)quinoline 58 6 7 °x / ° Y Y Y Y Y IT   ^=^0^ 1-(3-((3,4-dimethoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4- yl)piperidin-4-ol 59 0 FCO^^^A^S?^^ Y Y Y Y Z1 IT    ^^^N02 4-([l,4'-bipiperidin]-l'-yl)-3-((4-nitrophenyl)sulfonyl)-6-(trifluoromethoxy)quinoline 60 7 °\ / ° Y Y Y Y Jl N02 4-(4-methyl-l,4-diazepan-l-yl)-3-((4-nitrophenyl)sulfonyl)-6-(trifluoromethoxy)quinoline 61 OH 6 7 0 0 F3C°x^^Y^YSY^. Y Y Y Y N^   Xx^^N02 l-(3-((4-nitrophenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol Ex. Structure Name 62 OH A ilxX XX ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4-hydroxypiperidin-1 -yl)quinoline-6 -carboxylate 63 o / =o 0-=0 '--\ zo ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxylate 64 J cyyyyy °\ o ethyl 4-([l,4'-bipiperidin]-r-yl)-3-((4-ethylphenyl)sulfonyl)quinoline-6-carboxylate 65 OH X V H0 uj XX 3-((4-ethylphenyl)sulfonyl)-4-(4-hydroxypiperidin-1 -yl)quinoline-6 -carboxylic acid 66 I o / ° O ^7 CrO — \ / ° 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxylic acid 67 J ° \ o ZE 4-([l,4'-bipiperidin]-l'-yl)-3-((4-ethylphenyl)sulfonyl)quinoline-6-carboxylic acid Ex. Structure Name 68 .0 f3co^^zyysyx5^°\ Y Y Y Y Y 3-((3,4-dimethoxyphenyl)sulfonyl)-N,N-diethyl-6-(trifluoromethoxy)quinolin-4-amine 69 HO. / \ ?H°\ / ° W 7X, 2-((3-((3,4-dimethoxyphenyl) sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)amino)ethan-1 -ol 70 ^x / 0H 7 °x / ° f3co^^XYsV^°\ Y Y Y Y Y 1-(3-((3,4-dimethoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4- yl)piperidin-3-ol 71 o 'o \ <Z) <o g 3-((3,4-dimethoxyphenyl)sulfonyl)-N, N-dipropyl-6-(trifluoromethoxy)quinolin-4-amine 72 uT n O / =< O on'       O ■ o / ° 2,2'-((3-((3,4-dimethoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4- yl)azanediyl)bis(ethan-1 -ol) 73 HO. / \ ^0. / ° ^Os^A^sCz^O^ W XX, 2-((3-((3,4-dimethoxyphenyl) sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)amino)ethan-1 -ol 74 ^^0^0 F3C0^X^zk^ S C^x / °X Y Y Y Y Y N,N-dibutyl-3-((3,4- dimethoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-amine Ex. Structure Name 75 OH c 7 °\ / ° °2N T T T X JL l-(3-((4-ethylphenyl)sulfonyl)-6-nitroquinolin-4-yl)piperidin-4-ol 76 XN"^\ ? °\ / ° O2 N X T X X JL 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6-nitroquinoline 77 c O2N XX J X JL 4-([l,4'-bipiperidin]-l’-yl)-3-((4- ethylphenyl)sulfonyl)-6-nitroquinoline 78 I1 ^0 zo O2 N XX T TJL N,N-diethyl-3-((4-ethylphenyl)sulfonyl)- 6-nitroquinolin-4-amine 79 / N ? °x / ° X JL T L JL 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4- (1H-1,2,4-triazol-1 -yl)quinoline 80 > o 2=° w . \\ / --\ yo ethyl 3-((4-ethylphenyl)sulfonyl)-4-(lH- 1,2,4-triazol-1 -yl)quinoline-6-carboxylate Ex. Structure Name 81 7 0 0 Y Y Y Y hr N,N-diethyl-3-((4-ethylphenyl)sulfonyl)- 6-(trifluoromethoxy)quinolin-4-amine 82 ^^.OH 7 0..0 Y Y Y Y X l-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-3-ol 83 Y Y Y Y Jl X / \ / 3-((4-ethylphenyl)sulfonyl)-6-methoxy-N-(4-methylpiperazin-1 -yl)quinolin-4-amine 84 J ( / 1 oz \___, op / o=\ o < ethyl 3-((4-ethylphenyl)sulfonyl)-4-((4-methylpiper azin-1 -yl) amino)quinoline -6-carboxylate 85 'o .0 z—(7 dp / o 3-((4-methoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (trifluoromethoxy)quinolin-4-amine 86 r\ 7 0..0 Y Y Y Y JL 3-((4-methoxyphenyl)sulfonyl)-4-(lH-1,2,4-triazol-1 -yl)-6- (trifluoromethoxy)quinoline 87 7 0 0 SY^Ss Y Y Y Y Jl N,N-dibutyl-3-((4-ethylphenyl)sulfonyl)- 6-(trifluoromethoxy)quinolin-4-amine Ex. Structure Name 88 o P <71 dp /     o o 3-((3,4-dimethoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (trifluoromethoxy)quinolin-4-amine 89 ^\\ N > ? °\ / ° Y T Y Y T 3-((3,4-dimethoxyphenyl)sulfonyl)-4-(1H-1,2,4-triazol-1 -yl) -6 -(trifluoromethoxy)quinoline 90 L 7Ho. 0 Y Y Y Y X IT    ^^^OCF3 N-(4-methylpiperazin-l -yl)-6-(trifluoromethoxy)-3-((4-(trifluoromethoxy)phenyl)sulfonyl)quinol in-4-amine 91 ¢01 N > ? °\ / ° W T^„, 4-( 1H-1,2,4-triazol-1 -yl)-6-(trifluoromethoxy)-3-((4-(trifluoromethoxy)phenyl)sulfonyl)quinol ine 92 J cp / o 3-((4-butoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (trifluoromethoxy)quinolin-4-amine 93 o 0~0-p° 0' o 3-((4-butoxyphenyl)sulfonyl)-4-(lH-1,2,4-triazol-1 -yl)-6- (trifluoromethoxy)quinoline 94 p ..0 O0 /      Zj o' 3-((4-methoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6-nitroquinolin-4-amine Ex. Structure Name 95 .OH Hl|l o o T T J Y Jl 2-((3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)amino)ethan-1 -ol 96 ? °\ / ° TT J T J ^CT^^IT 3-((3,4-dimethoxyphenyl)sulfonyl)-6,7-dimethoxy-4-( 1H-1,2,4-triazol-1 -yl)quinoline 97 rP / --\ Z     / )—H   | / / \0 0'° o 3-((4-methoxyphenyl)sulfonyl)-6-nitro-4- (1H-1,2,4-triazol-1 -yl)quinoline 98 ^\\ N. > ? °x / ° nc^CoT1 2-(3-((4-methoxyphenyl)sulfonyl)-4-(lH-1,2,4-triazol-1 -yl)quinolin-6- yl) acetonitrile 99 L ^N. Tv NC"'O 2-(3-((4-methoxyphenyl)sulfonyl)-4-((4-methylpiperazin-1 -yl)amino)quinolin-6-yl) acetonitrile 100 F3C0^^ / L^SYz^ T T J T X N,N-diethyl-2-(4-(3-((4- ethylphenyl)sulfonyl)-6- (trifluoromethoxy)quinolin-4-yl)-l,4-diazepan-1 -yl)ethan-1 -amine Ex. Structure Name ^"O N,N-diethyl-2-(( 1-(3-((4- 101 A ethylphenyl)sulfonyl)-6- k 4 0 (trifluoromethoxy)quinolin-4- F3CO^x Y Till yl)piperidin-4-yl)oxy)ethan-1 -amine OH A 0 l'-(3-((4-ethylphenyl)sulfonyl)-6- 102 f3co^ II A Ar      ii A (trifluoromethoxy)quinolin-4-yl)-[ 1,4'-bipiperidin]-4-ol H j [i 103 kJ N,N-diethyl-1-(3 -((4-ethylphenyl)sulfonyl)-6- F3COx / Y 7 0..0 ^XX Y Y Y ? (trifluoromethoxy)quinolin-4-yl)piperidin-4-amine hr   x^X / HO—i 5-((3-((4-ethylphenyl)sulfonyl)-6- 104 f3cox / T T J T X (trifluoromethoxy)quinolin-4-yl) amino)pentan-1 -ol N 3-((4-ethylphenyl)sulfonyl)-N-(piperidin- 105 F3co^ / x AX / x l-yl)-6-(trifluoromethoxy)quinolin-4- Y Y Y Jl amine Ex. Structure Name 106 uT n O / / I -\ zo 3-((4-ethylphenyl)sulfonyl)-N-(pyridin-4-ylmethyl)-6-(trifluoromethoxy)quinolin-4-amine 107 ^0 0 F3C0^^XxA s Y Y Y Y Jl 3-((4-ethylphenyl)sulfonyl)-N-(pyridin-4-yl)-6-(trifluoromethoxy)quinolin-4-amine 108 o 7 0..0 Y Y Y Y JL 3-((4-ethylphenyl)sulfonyl)-4-(lH-pyrrol-l-yl)-6-(trifluoromethoxy)quinoline 109 nD Y Y Y Y JL 3-((4-ethylphenyl)sulfonyl)-4-(lH-pyrazol-l-yl)-6-(trifluoromethoxy)quinoline 110 n-a ? °\ / ° w x 3-((4-ethylphenyl)sulfonyl)-4-( 1H-1,2,3 -triazol- l-yl)-6- (trifluoromethoxy)quinoline 111 HO |H°xz° Y Y Y Y 4-((3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)amino)butan-l -ol Ex. Structure Name 112 YY- n 7 0 0 FaCO^^x^Ys Y Y Y Y Ji 4-(lH-benzo[d][l,2,3]triazol-l-yl)-3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinoline 113 OH 0 F / O^ / xXj^Y^ Y Y Y Y ? IT l'-(3-((4-methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-[ 1,4'-bipiperidin]-4-ol 114 c 3. .0 °2 n                s Y Y Y Y 4-([l,4'-bipiperidin]-l'-yl)-3-((4-methoxyphenyl)sulfonyl)-6-nitroquinoline 115 2 w-CD^O x° 0' o \ 2-(4-( [ 1,4'-bipiperidin] -l'-yl)-3-((4-methoxyphenyl)sulfonyl)quinolin-6-yl) acetonitrile 116 / \ o o ,0 v3" o^ 4-( [ 1,4'-bipiperidin] -1 '-yl)-6-butoxy-3-((3,4- dimethoxyphenyl)sulfonyl)quinoline Ex. Structure Name 117 7 °x / ° IT Y Y J] 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl- 1 H-imidazol-1 -yl)-6-(trifluoromethoxy)quinoline 118 h ? °\ / ° wu 3-((4-ethylphenyl)sulfonyl)-4-(lH-imidazol-l-yl)-6-(trifluoromethoxy)quinoline 119 6 7 °x / ° 4-([l,4'-bipiperidin]-l’-yl)-3-((4-butoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinoline 120 0 Y Y Y Y Ji ^^X'OCF3 4-([l ,4'-bipiperidin]-1 '-yl)-6- (trifluoromethoxy)-3-((4- (trifluoromethoxy)phenyl)sulfonyl)quinol ine 121 0.., / s^^YYs^^°\ Y Y Y Y Y IT 4-( [ 1,4'-bipiperidin] -1 ’-yl)-3-((3,4-dimethoxyphenyl)sulfonyl)-6-(methylthio)quinoline 122 / \ o o / \ / \ \   2—\   z—\ °\ / ° 4-( [ 1,4'-bipiperidin] -1 ’-yl)-3-((3,4-dimethoxyphenyl)sulfonyl)-6,7 -dimethoxyquinoline Ex. Structure Name 123 V- 6-butoxy-3-((3,4- dimethoxyphenyl)sulfonyl)-N,N-diethylquinolin-4-amine 124 ? °x / ° Y Y Y YA N,N-dibutyl-3-((3,4- dimethoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-amine 125 N—N 7 0 O y y Y YA 3-((4-ethylphenyl)sulfonyl)-4-(lH-tetrazol-l-yl)-6-(trifluoromethoxy)quinoline 126 n O / =( / -° O O 0 r N-(3 -((4-ethylphenyl)sulfonyl) -6-(trifluoromethoxy)quinolin-4-yl)morpholin-4-amine 127 0 H0 J ? °x / ° F<c0 Y Y Y YA 4-(4-ethylphenyl)-1-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol 128 o / =° O 5 AzYAA >—'—< ethyl 4-(4-(4-ethylphenyl)-4-hydroxypiperidin-1 -yl) -3 -((4-ethylphenyl)sulfonyl)quinoline-6-carboxylate Ex. Structure Name 129 0 hoU" ? °\z° Y T Y TO 4-(4-ethylphenyl)-1-(3-((4-methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol 130 OH 0 1 ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4-hydroxy-[ 1,4’-bipiperidin] -1’- yl)quinoline-6-carboxylate 131 Yo X 10v° ethyl 4-(4-(2-(diethylamino)ethyl)-l,4-diazepan-l-yl)-3-((4- ethylphenyl)sulfonyl)quinoline-6- carboxylate 132 A X^V ^lXTXX ethyl 4-(4-(2- (diethylamino)ethoxy)piperidin-1 -yl)-3 -((4-ethylphenyl)sulfonyl)quinoline-6-carboxylate 133 n H 1 o \____. o=\ o < ethyl 4-( 1 H-benzo[d] [ 1,2,3] triazol-1 -yl)-3-((4-ethylphenyl)sulfonyl)quinoline-6-carboxylate Ex. Structure Name 134 n 1 JLV lXT YY ethyl 3-((4-ethylphenyl)sulfonyl)-4-(lH-imidazol-1 -yl)quinoline-6-carboxylate 135 o / =° Rx Y ethyl 3-((4-ethylphenyl)sulfonyl)-4-(3-hydroxypiperidin-1 -yl)quinoline-6 -carboxylate 136 0 X V ^°XXXXXX ethyl 4-([l,4'-bipiperidin]-r-yl)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate 137 I I v ^YYd YY ethyl 4-(3-hydroxypiperidin-l-yl)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate 138 OH 0 X ^°V° iCo XX ethyl 4-(4-hydroxy- [ 1,4'-bipiperidin] -1'-yl)-3-((4- methoxyphenyl)sulfonyl)quinoline-6-carboxylate 139 o ^=° VyXj 0' o \ ethyl 4-(4-(2-(diethylamino)ethyl)-l,4-diazepan-l-yl)-3-((4- methoxyphenyl)sulfonyl)quinoline-6- carboxylate Ex. Structure Name 140 1 Xi ■ n JO ethyl 4-(4-(2- (diethylamino)ethoxy)piperidin-1 -yl)-3 -((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate 141 N-j <3 X Xv iQo TH ethyl 4-(lH-imidazol-l-yl)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate 142 N— " \\ / / N I 1V cXT VI ethyl 4-( 1 H-benzo[d] [ 1,2,3] triazol-1 -yl)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate 143 0 0 H 11 J 11 4-([l,4’-bipiperidin]-r-yl)-3-((4-methoxyphenyl)sulfonyl)-N-methylquinoline-6-carboxamide 144 \ N—\ a XY xTX 1X1 ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(4-methyl-l,4-diazepan-l-yl)quinoline-6-carboxylate 145 xo 0 h°X 7 °\ / ° XT J [T JL l-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-4-(4-methoxyphenyl)piperidin-4-ol Ex. Structure Name 146 u HO J 7 0..0 Y Y J T JL l-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-4-(3-methoxyphenyl)piperidin-4-ol 147 o 1. M h° J 7 0 0 T Y Y YA 4-(benzo[d] [ 1,3]dioxol-5-yl)-l -(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol 148 o / =° zw zYvj ° x° r ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4- hydroxy-4-(4-methoxyphenyl)piperidin- 1 -yl)quinoline-6-carboxylate 149 YJ hoY 2       7 °x / ° °ATYY YY ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4- hydroxy-4-(3-methoxyphenyl)piperidin- 1 -yl)quinoline-6-carboxylate 150 M hoJ Y Y Y Y Y X—^0^ 4-(3-methoxyphenyl)-l-(3-((4-methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol Ex. Structure Name 151 \___ / o 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)-6-(trifluoromethoxy)quinoline 152 OH d c-0- XX J LA — N    — 0 — l'-(3-((4-butoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-[ 1,4'-bipiperidin]-4-ol 153 \n H    / )-H    )-H    )—O / /  \__ /  \__ / I A o / ° l'-(3-((3,4-dimethoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)- [ 1,4'-bipiperidin]-4-ol 154 \ Q, / s mm / LL XT T XT 3-((3,4-dimethoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)-6- (methylthio)quinoline 155 i XT XTO ethyl 4-(dibutylamino)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate 156 > o / =° mA Am A o 0' ' o \ ethyl 4-(bis(2-hydroxyethyl)amino)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate Ex. Structure Name 157 o 2=0 O x° 0' ethyl 4-([ 1,4’-bipiperidin]-1 ’-yl)-3-((4-butoxyphenyl)sulfonyl)quinoline-6-carboxylate 158 \--X °        1 0^,0 0 uu IX ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxylate 159 0 9-TTY YJ bT 4-([l,4’-bipiperidin]-r-yl)-3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinoline 160 \r—\ 9- IT Y Y 1 1 / 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)-6-(methylthio)quinoline 161 OH 0 8    T».,» / - Az^XX / ^ N    ^^ 0    \ ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-hydroxy-[ 1,4’-bipiperidin] -1’- yl)quinoline-6-carboxylate 162 OH 0 9-T Y Y Y ? l’-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)- [ 1,4’ -bipiperidin]-4-ol Ex. Structure Name 163 -K +Y Y Y T Y 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)-6-(methylsulfinyl)quinoline 164 '0 Ok / °       1 0. a 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)-6-(methylsulfonyl)quinoline 165 \ N—\ X XY N,N-diethyl-3-((4-methoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxamide 166 \ N^. ''''I          9         7 °\ / ° ..                A H UY UU N            0 N-(2-(diethylamino)ethyl)-3-((4-methoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxamide 167 ^o O—on + \ 4-([l,4'-bipiperidin]-l’-yl)-3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinoline 168 OH 0 XXx N         O — l'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin]-4-ol Ex. Structure Name 169 0 6 x TXT TX 4-([l,4'-bipiperidin]-l’-yl)-3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfonyl)quinoline 170 OH i "Co XX N         0— l'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfonyl)quinolin-4-yl)- [ 1,4'-bipiperidin]-4-ol 171 \ O ..0 -yy-yy yy o=\ o < ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)piperidin-1 -yl)quinoline-6-carboxylate 172 6 N U        ? °s z° 0 uu XX ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)piperidin-1 -yl)quinoline-6-carboxylate 173 o A ^°V° lYj Xl ethyl 4-(4-(azepan-1 -yl)piperidin-1 -yl)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate Ex. Structure Name 174 X ^°v° ethyl 4-(3-hydroxy- [ 1,4’-bipiperidin] -1’-yl)-3-((4- methoxyphenyl)sulfonyl)quinoline-6-carboxylate 175 > o / =° W     g ZW zvJ zlJ x° 0' o \ ethyl 4-(4-(hydroxymethyl)-[l ,4’- bipiperidin]-l’-yl)-3-((4- methoxyphenyl)sulfonyl)quinoline-6-carboxylate 176 o 0 N          0  — ethyl 4-(4-(azepan-1 -yl)piperidin-1 -yl)-3-((4-butoxyphenyl)sulfonyl)quinoline-6-carboxylate 177 / x^oh o   ^—1 n ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(3-hydroxy-[ 1,4’-bipiperidin] -1’- yl)quinoline-6-carboxylate 178 fi o < ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(hydroxymethyl)-[ 1,4’-bipiperidin] -1’-yl)quinoline-6-carboxylate 179 N—\ 8 J v° uj Vl ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(4-(2-(piperidin-l -yl)ethyl)-l ,4-diazepan- 1 -yl)quinoline-6-carboxylate Ex. Structure Name 180 N X aV ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(4-(2-(pyrrolidin-l -yl)ethyl) -1,4-diazepan-1 -yl)quinoline-6-carboxylate 181 N"^ fl          1 <\,o ° OCu 0, / ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(2-(piperidin-1 -yl)ethyl)-1,4-diazepan-1 -yl)quinoline-6-carboxylate 182 ^~-r? N-'X 0      '“-N o n ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(2-(pyrrolidin-1 -yl)ethyl)-1,4-diazepan-1 -yl)quinoline-6-carboxylate 183 X ,N 1 Iv lXT XI ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(1H-1,2,4-triazol-1 -yl)quinoline-6-carboxylate 184 / / N ^An A A °V° ^XXXXl ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(1H-1,2,3-triazol-1 -yl)quinoline-6-carboxylate 185 N—N A   A 0V° ethyl 3-((4-methoxyphenyl)sulfonyl)-4- (1 H-tetrazol-1 -yl)quinoline-6-carboxylate Ex. Structure Name 186 N—N fl          1 <\,0 uu 0.. N             0 ethyl 3-((4-butoxyphenyl)sulfonyl)-4- (1 H-tetrazol-1 -yl)quinoline-6-carboxylate 187 8 ^0 0 o 4-(3-((4-butoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)thiomorpholine 188 < ZN I IV ^°00j l\T ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1H-1,2,4-triazol-1 -yl)quinoline-6-carboxylate 189 N—A X X Y lYo XX ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1H-1,2,3-triazol-1 -yl)quinoline-6-carboxylate 190 < N I Iv xYLX ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1H-1,2,4-triazol-1 -yl)quinoline-6-carboxylate 191 / o \=o O Co CX Of 0 o ethyl 3-((4-butoxyphenyl)sulfonyl)-4- thiomorpholinoquinoline-6-carboxylate 192 \ N—\ 1 n          i oxzo A / v WV 00 H LX. J LX. 3-((4-butoxyphenyl)sulfonyl)-N-isopropyl-4-(4-methyl-1,4-diazepan-1 - yl)quinoline-6-carboxamide Ex. Structure Name 193 \ 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)-N -((4R,5S,6R)-2,4,5 -trihydroxy-6 -(hydroxymethyl)tetrahydro-2H-pyran-3-yl)quinoline-6-carboxamide 194 i V- 0 iYj YY l\T ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1 H-imidazol-1 -yl)quinoline-6-carboxylate 195 o’ 6 1  1 V lTT Y1 ethyl 3-((4-butoxyphenyl)sulfonyl)-4-( 1 -oxidothiomorpholino)quinoline-6-carboxylate 196 o \=o O rynf cY 0' o ethyl 3-((4-butoxyphenyl)sulfonyl)-4- (1,1 -dioxidothiomorpholino)quinoline-6 -carboxylate 197 o Z1—O \\ / / \___ / ' x° 0' o 4-(3-((4-butoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4- yl)thiomorpholine 1-oxide 198 Ox / ,° 0 7 °x / ° FgCO^^x^LY^^x Y Y Y Y IT  \tTZW 4-(3-((4-butoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4- yl)thiomorpholine 1,1-dioxide 199 \ N^\ X X°v° jlXj T1 3-((4-butoxyphenyl)sulfonyl)-N,N-diethyl-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxamide Ex. Structure Name 200 \ o S ox / o H IL J J L A 3-((4-butoxyphenyl)sulfonyl)-N-(2-hydroxyethyl)-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxamide 201 A ^V° ^Ln iCo Li /   / / ^N^   / / g-^ / ^ / 4-([l,4'-bipiperidin]-l'-yl)-3-((4-butoxyphenyl)sulfonyl)-N,N -diethylquinoline-6-carboxamide 202 0 n       f °\z° ho.   A   A A z / n A^A^A" "t A H W LX / / / / N    AA^^q^AA A. 4-([l,4'-bipiperidin]-l'-yl)-3-((4-butoxyphenyl)sulfonyl)-N-(2-hydroxyethyl)quinoline-6-carboxamide 203 0 H       ? °\z° / / A^A>t^ N ii A^A ii A H LX J LX / / / / a^ N    A^^O a^ a 4-([l,4'-bipiperidin]-l'-yl)-3-((4-butoxyphenyl)sulfonyl)-N-ethylquinoline-6-carboxamide 204 o “   J     1 ^AA / nAAAy "v^A ho^A^ h H      \ H JL OH   ------ 4-( 1 H-imidazol-1 -yl)-3-((4- methoxyphenyl)sulfonyl)-N-((4R, 5 S, 6R) -2,4,5-trihydroxy-6- (hydroxymethyl)tetrahydro-2H-pyran-3-yl)quinoline-6-carboxamide 205 " \\ / / Ns o °h 8 I h°—AtnaVY VA hA / h 1! A J  II A ^- OH / / / N /    / ^^0^ 4-(lH-benzo[d][l,2,3]triazol-l-yl)-3-((4-methoxyphenyl)sulfonyl)-N-((4R, 5 S, 6R) -2,4,5-trihydroxy-6- (hydroxymethyl)tetrahydro-2H-pyran-3-yl)quinoline-6-carboxamide Ex. Structure Name 206 \ YY (Z> 0' 3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)-4-(4-(2-(piperidin-1 - yl) ethyl) -1,4-diazepan-1 -yl)quinoline 207 N-^x 9- Y Y Y Y J [T   Xs^q^X / X^ 3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)-4-(4-(2-(pyrrolidin-1 -yl) ethyl) -1,4-diazepan-1 -yl)quinoline 208 \ + <zi—O uy                 O 0'    ' l'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin]-3-ol 209 f A°v° x+YVj Yi 00V X^cXz^ 3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(piperidin-1 -yl) ethyl) -1,4-diazepan-1 -yl)quinoline 210 N-^x ? A°v° / +tyy vi Xs^N-^ xXqX / x 3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(pyrrolidin-1 -yl) ethyl) -1,4-diazepan-1 -yl)quinoline 211 \ N—\ 0 H   0°xz° ° UJ ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-methyl-1,4-diazepan-1 -yl)piperidin-1 -yl)quinoline-6-carboxylate Ex. Structure Name 212 0 N A^A 0 uJ N            0 ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-morpholinopiperidin-l-yl)quinoline-6-carboxylate 213 •r 0 / x A A A 0 CO A ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-fluorophenyl)piperazin-1 -yl)quinoline-6-carboxylate 214 . .0 o C°A o ( ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-(2 -hydroxy ethyl)piperazin-1 -yl)piperidin-1 -yl)quinoline-6-carboxylate 215 ..0 A o < ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-phenyl-[ 1,4'-bipiperidin] -1 '-yl)quinoline-6-carboxylate 216 ..0 o < ethyl 4-([l,4':r,4"-terpiperidin]-l"-yl)-3-((4-butoxyphenyl)sulfonyl)quinoline-6-carboxylate Ex. Structure Name 217 .0 o ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-thiomorpholinopiperidin-1 -yl)quinoline-6-carboxylate 218 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)-6- (methylthio)quinoline 219 o ..0 4-([l,4'-bipiperidin]-l’-yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline 220 o ,.0 o—+ \ 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)-6- (methylsulfinyl)quinoline 221 0 XXX O / x^x / x / 4-([l,4'-bipiperidin]-l'-yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 222 / \.oh ^hT 6 '’W'V l'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)- [ 1,4'-bipiperidin]-3-ol Ex. Structure Name 223 OH 0 l'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)- [ 1,4'-bipiperidin]-4-ol 224 \ + ^-O , o l'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin]-4-ol 225 o p° / qp zCp '--\ zo 0' o \ ethyl 3-((4-methoxyphenyl)sulfonyl)-4-((4-methylpiperazin-1 - yl)amino)quinoline-6-carboxylate 226 <Z>            / 0 O / X x° 0° o 3-((4-methoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6-(methylthio)quinolin-4-amine 227 hP — O , / 0 o / X x° <0 o 3-((4-methoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (methylsulfinyl)quinolin-4-amine 228 L .N^ 0..0     nHq o ¥ T T ¥ 7l 3-((4-methoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (methylsulfonyl)quinolin-4-amine Ex. Structure Name 229 0 2. Y Y Y Y Jl 4-( 1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)piperidin-4-yl)morpholine 230 \ IZ) 5> — \ / ° — — 0' 2-(4-(1-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1 -ol 231 0 5 0. Y Y Y Y JI 4-([l,4':r,4"-terpiperidin]-l"-yl)-3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinoline 232 =,0 .----< o ,----,      ,----, °' \---- V K / \ / —\ 2—\ 2—\ Z l'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-4-phenyl-[ 1,4'-bipiperidin] -4-ol 233 0 0 6 ? °\ / ° Y Y Y Y X 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-(4-fluorophenyl)piperazin-1 -yl)piperidin-1 -yl) -6 -(methylthio)quinoline Ex. Structure Name 234 J’ 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-methyl-1,4-diazepan-1 -yl)piperidin-1 -yl)-6-(methylthio)quinoline 235 \ + O — \ / ° — — 4-( 1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)piperidin-4-yl)morpholine 236 \ +   O V / V7 VJ 2-(4-(1-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1 -ol 237 ._____.          ._____.          ._____. oz \_____. /  \   /  \   /  \ \   2—\   2—\   2—\   2 1 O—<z> + \ 4-([l,4':r,4"-terpiperidin]-l"-yl)-3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinoline 238 \ + GO—O w"hO“OtO 0' l'-(3-((4-butoxyphenyl)sulfonyl)-6- (methylsulfinyl)quinolin-4-yl)-4-phenyl-[ 1,4'-bipiperidin] -4-ol Ex. Structure Name 239 \ + 0' 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-(4-fluorophenyl)piperazin-1 -yl)piperidin-1 -yl) -6 -(methylsulfinyl)quinoline 240 OH 6 ?       ? 0 0 +ITJ (l'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)methanol 241 \ N—< o X-Jxxx CCJC 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-methyl-1,4-diazepan-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline 242 Tn y a o N,N-diethyl-2-(4-((4-(4-methyl-1,4-diazepan-l-yl)-6-(methylthio)quinolin-3-yl)sulfonyl)phenoxy)ethan-1 -amine 243 y CO _____.        .____. oz \ . / \   /  \ co    2--(    2--a    z CO \ 4-( 1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)piperidin-4-yl)thiomorpholine - 128 - 249 248 247 246 245 244 Ex. \ 0 0' o <         O &  ’ o 6 6 7 °x / ° UU \ + on —O ! / / \ / \__ / — \ / ° — — & o / ° w 71-0 , ¥ 0' 0^ Structure 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-methyl-1,4-diazepan-1 -yl)piperidin-1 -yl) -6 -(methylthio)quinoline 3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)-4-(4-(2-(piperidin-1 -yl) ethyl) -1,4-diazepan-1 -yl)quinoline l'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)- [ 1,4'-bipiperidin]-3-ol 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)piperidin-1 -yl) -6-(methylthio)quinoline 4-( 1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)piperidin-4-yl)thiomorpholine ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(1 -oxidothiomorpholino)piperidin-1 -yl)quinoline-6-carboxylate Name WO 2021 / 076886                                                 PCT / US2020 / 055979 Ex. Structure Name 250 <O o, O 0° o 2-(4-(1-(3-((4- (heptyloxy)phenyl)sulfonyl)-6- (methylthio)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1 -ol 251 4>00 0' o 4-([l,4’:r,4"-terpiperidin]-l"-yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline 252 6 "'ayu.™ 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-methylpiperazin-1 -yl)-6-(methylthio)quinoline 253 6 N XX / 3^ N          q '-y' \X 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)piperidin-1 -yl) -6-(methylsulfinyl)quinoline 254 \ y-O , hx>Q 0° S o l’-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4’-bipiperidin]-3-ol 255 \ + o & / C / > 0* o 3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(piperidin-1 -yl) ethyl) -1,4-diazepan-1 -yl)quinoline - 130 - WO 2021 / 076886                                                 PCT / US2020 / 055979 Ex. Structure Name 263 J o—+ \ l'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-4-phenyl-[ 1,4’-bipiperidin] -4-ol 264 6 N 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiper azin-1 -yl)piperidin-1 -yl) -6 -(methylsulfinyl)quinoline 265 / X^OH l’-(3-((4-(decyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4’-bipiperidin]-3-ol 266 N—X 3-((4-(decyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(piperidin-1 -yl) ethyl) -1,4-diazepan-1 -yl)quinoline 267 '0 °"             n 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(4-methyl-1,4-diazepan-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline 268 H0'XX^ 0 N 2-(4-(1-(3-((4- (decyloxy)phenyl) sulfonyl)-6 - (methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1 -ol - 132 - WO 2021 / 076886                                                 PCT / US2020 / 055979 Ex. Structure Name 275 0^0, Q, oxx_ 4-(4-(( 1 -benzylpiperidin-4-yl)methyl)piperazin-1 -yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline 276 Q 3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(pyrrolidin-1 -yl)ethyl)piperazin-1 -yl)quinoline 277 \-o 0' o 4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 278 rv^ ■ 0 S XV° XuXlzx / w 4-(4-(1 -benzylpyrrolidin-3 -yl)piperazin-l-yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 279 OX - 0 0       N n n 'WX_ 4-(4-(( 1 -benzylpiperidin-4-yl)methyl)piperazin-1 -yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 280 |X^OmPEG 0 N 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-(2-mPEGoxyethyl)piperazin-1 -yl)piperidin-1 -yl) -6 -(methylsulfinyl)quinoline Ex. Structure Name 281 J \ 3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)-4-(4-(2-(piperidin-1 -yl)ethyl)piperazin-1 -yl)quinoline 282 \ + <z>—O fix° 0' o 3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(piperidin-1 -yl)ethyl)piperazin-1 -yl)quinoline 283 0 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(l-ethylpiperidin-4-yl)piperazin-l-yl)-6-(methylsulfinyl)quinoline 284 0 N 2-(4-(1-(3-((4-((3,7- dimethyloctyl)oxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1 -ol 285 6 0 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4’-bipiperidin] -l’-yl)-6-(methylsulfinyl)quinoline 286 0 N 0 4-( 1 ’-(3-((4-(decyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)- [ 1,4’-bipiperidin] -4-yl)morpholine Ex. Structure Name 287 \ 0 0 °"             n 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(4-methyl-1,4-diazepan-1 -yl)- [ 1,4’-bipiperidin]-l’-yl)-6- (methylsulfinyl)quinoline 288 6 1 "-(3 -((4-(decyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4’:r,4"-terpiperidin] -3 -ol 289 X-o -¾ X >< > 0' o 4-([l,4':r,4"-terpiperidin]-l"-yl)-3-((4-((3,7- dimethyloctyl)oxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 290 0 0 4-([l,4':r,4"-terpiperidin]-l"-yl)-3-((4-(decyloxy) -3 -fluorophenyl) sulfonyl) -6 -(methylsulfinyl)quinoline 291 HO'X^ 0 N 2-(4-(1 -(3-((4-(decyloxy)-3- fluorophenyl)sulfonyl) -6- (methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1 -ol 292 0 2-(4-(l’-(3-((4- (decyloxy)phenyl) sulfonyl)-6 - (methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)piperazin-1 -yl)ethan-1 -ol Ex. Structure Name 293 0 1 H .o.       A. II 1 J o H n IT N,N-diethyl-6,7 -dimethoxy-3 -((4-methoxyphenyl)sulfonyl)quinolin-4-amine 294 0 1 H .o.       A. >i Xr      " ti X II 1 J o H   n IT   X^o^ N-ethyl-N-isopropyl-6,7-dimethoxy-3 -((4-methoxyphenyl)sulfonyl)quinolin-4-amine 295 N 1 H A. X, x< xxiiXf x, JU J J 0 U A Xd^^^^IT N,N-dibutyl-6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinolin-4-amine 296 X^x, 0 1 II ^o.            .s. Y Y xxii y x JI J J o [|l Nl-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)-N1 ,N2,N2-triethylethane-1,2-diamine 297 \ o 0 0=^=0 n w '      o o \ / Nl-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)- N2,N2-diethylethane-l ,2-diamine 298 /   ^NH 0 1 H XXT°Ti Nl-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)-N3 ,N3 -diethylpropane-1,3 -diamine Ex. Structure Name 299 \ o 0 O=o9=O / —z     O O Nl-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)- N4,N4-diethylbutane-1,4-diamine 300 \ o 0 0=09=0 2--X     /   \ (    ' O    O \ \ / N3-(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinolin-4-yl)-N1 ,N 1 -diethylbutane-1,3 -diamine 301 \ o 0 0 = 09 = 0 < ” ft o o \ / 2-(4-(6,7-dimethoxy-3 -((4- methoxyphenyl)sulfonyl)quinolin-4-yl)piperazin-1 -yl)ethan-1 -ol 302 0 N 0 1 H .0.      / 0 .s. X Ti            11 T Y A Jl J 01A 3-(4-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)piperazin-l -yl)-N,N-diethylpropan-1 - amine 303 o \ >Y. 0=09=0 O 1 -(6,7 -dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)piperidin-4-ol 304 / \ o o A O=(Z)=O 0 o \ (1-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)piperidin-3 -yl)methanol Ex. Structure Name 305 HO V. 1 II 1 -(6,7 -dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)pyrrolidin-3-ol 306 ' A 1ST 0 1 II TYj7 YX 6,7-dimethoxy-3 -((4-methoxyphenyl)sulfonyl)-4-(( 1S ,4S)-5 -methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)quinoline 307 \ / / ° N—V o. 1                >1 / 0.     ^k / S. YXXXlI 4-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)-N,N-dimethyl-l ,4-diazepane-l -carboxamide 308 / \ o o '1 < >? 0=1 / 1=0 0 o \ 1 -(6,7 -dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)- 4-phenylpiperidin-4-ol 309 °<^°\ 0 0 ca>x methyl 4-(1-(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinolin-4- yl)piperidin-4-yl)benzoate Ex. Structure Name 310 H 0 0 1 H .o.      A .s. X Ti              11 T JI J J 0 [1 J 4-( 1 -(6,7-dimethoxy-3 -((4- methoxyphenyl)sulfonyl)quinolin-4- yl)piperidin-4-yl) -N-methylbenzamide 311 0 1 II XXj8YX 6,7-dimethoxy-4-(4-(4- methoxyphenyl)piperidin-1 -yl)-3-((4-methoxyphenyl)sulfonyl)quinoline 312 Q o I ii .0.       / k .S. VXjPXI 6,7-dimethoxy-3 -((4-methoxyphenyl)sulfonyl)-4-(4-(4-(pyrrolidin-1 -ylmethyl)phenyl)piperidin-l-yl)quinoline 313 o XNX 0 1 II / 0.     A. YJCJoYJi N         0^ 6,7-dimethoxy-3 -((4-methoxyphenyl)sulfonyl)-4-(3-phenylpyrrolidin-1 -yl)quinoline 314 ° XNX 0 1 II YJo°Vl N x 4-(3-(benzo[d][l,3]dioxol-5- yl)pyrrolidin-l-yl)-6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinoline Ex. Structure Name 315 \ o 0 0=^=0 o o \ / 6,7-dimethoxy-3 -((4-methoxyphenyl)sulfonyl)-4-(4-phenylpiperazin-1 -yl)quinoline 316 ¢ ^l\T   0 1          H XL ii                        11    ii II   1   J 0  [1 1 IT 6,7-dimethoxy-4-(4-(4-methoxyphenyl)piperazin-1 -yl)-3-((4-methoxyphenyl)sulfonyl)quinoline 317 0 N 0 1 H YXY°7n ethyl 4-(4-(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinolin-4-yl)piperazin-1 -yl)benzoate 318 0^ ¢ o N N   0 1          H 7i                        ||   ii II 1 J o H n 4-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)-l-(4-methoxyphenyl)piperazin-2-one Ex. Structure Name 319 O=V1 = O b’ '—'            o o \ / N-cyclohexyl-4-(4-(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinolin-4-yl)piperazin-1 -yl)benzamide 320 0 0. 1 II / k YYY oYk 4-( [ 1,4’-bipiperidin] -1 ’-yl)-6,7 -dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinoline 321 ¢. 1              II / 0.           _S. Il                           11    Tl        J JI J J 0 |l  A 1-(1 -(6,7-dimethoxy-3 -((4- methoxyphenyl)sulfonyl)quinolin-4- yl)piperidin-4-yl)pyrrolidin-2-one 322 / \ o o O = cn=O 0 o \ (1-(1-(6,7-dimethoxy-3 -((4-methoxyphenyl)sulfonyl)quinolin-4-yl)piperidin-4-yl)pyrrolidin-2-yl)methanol 323 / \ o o       o J o O=c^=O O \ 2-(4-(6,7-dimethoxy-3 -((4- methoxyphenyl)sulfonyl)quinolin-4-yl)-1,4-diazepan-1 -yl)ethan-1 -ol 324 / \ o o y<jj 0 o \ 7-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)-1 -isobutyldecahydropyrido[4,3- e][l,4]oxazepine Ex. Structure Name 325 OH 0 1 II .o.       A. ,s. TXT 1 -((4-(6,7-dimethoxy-3 -((4- methoxyphenyl)sulfonyl)quinolin-4-yl)- 1,4-diazepan-1 -yl)methyl)cyclopentan-1 -ol 326 N 0 1 II XXJ°X1 6,7-dimethoxy-3 -((4- methoxyphenyl)sulfonyl)-4-(4-(oxetan-3-yl)-1,4-diazepan-l -yl)quinoline 327 Cl N^\ N--\ '—N 0 1 II YXTST1 IT 6-chloro-2-(4-(6,7 -dimethoxy-3 -((4-methoxyphenyl)sulfonyl)quinolin-4-yl)-1,4-diazepan-1 -yl)benzo[d] thiazole 328 0 \A N 0 1 H / k 7i                  II 7f II J J o 11 J 1 -(6,7 -dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)-4-methyl-l ,4-diazepan-5-one 329 CD     O ^Ul^j 0—^—0 O\ 6,7-dimethoxy-3 -((4-methoxyphenyl)sulfonyl)-4-(4-(tetrahydro-2H-thiopyran-4-yl)-1,4-diazepan- 1 -yl)quinoline Ex. Structure Name 330 0 ii _ O=S-^ 0 1 H ^x A. 11 1 J 0 |l IT 4-(4-(6,7-dimethoxy-3 -((4- methoxyphenyl)sulfonyl)quinolin-4-yl)-1,4-diazepan-1 -yl)tetrahydro-2H-thiopyran 1,1-dioxide 331 0 0            0 II                              1 II \ X xx x<x N Ti ^T        " ti 1         J 0 IL JI x / x N    X / Xg^ 4-([l,4’-bipiperidin]-l’-yl)-3-((4-methoxyphenyl)sulfonyl)-N,N -dimethylquinoline-6-carboxamide 332 0            0 II                                1 II X / X N >< Xf x< II >< 1 L JL J 0 IL JL 3-((4-methoxyphenyl)sulfonyl)-N,N-dimethyl-4-(4-(2-oxopyrrolidin-l-yl)piperidin-1 -yl)quinoline-6-carboxamid 333 / _-N N-^\ ° / 1 0       NZ 0 II                                  1                II x   ^x N Ti                  H Ti 1 I J ° I Jx 4-(4-(2-(dimethylamino)-2-oxoethyl)-1,4-diazepan- l-yl)-3-((4-methoxyphenyl)sulfonyl)-N,N -dimethylquinoline-6-carboxamide 334 0 0           0 II                              1 II x x^x ^<x N     Ti xp         II Ti H   IL J^ J 0 IL JL 4-([l,4'-bipiperidin]-l’-yl)-3-((4-methoxyphenyl)sulfonyl)-N-methylquinoline-6-carboxamide 335 \'"'''X. 0       NZ 0 II                        1 H X Jk N 7|                    II Ti H IL JL J 01JL 3-((4-methoxyphenyl)sulfonyl)-N-methyl-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxamide Ex. Structure Name 336 NX o            o Il                            l ii \         A. ,s. N     T                 II  Ti H   IL JI J 0 II J 4-(4-(2-(hydroxymethyl)pyrrolidin-1 -yl)piperidin-l -yl)-3 -((4-methoxyphenyl)sulfonyl)-N-methylquinoline-6-carboxamide 337 J     °        0 \ .N.      41      A. .5.. H 11J^ J 0 11J^ 4-( [ 1,4'-bipiperidin] -1 '-yl)-N-(2-(diethylamino)ethyl) -3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxamide 338 3 0           0 N-(2-(diethylamino)ethyl)-4-( 1 -isobutyloctahydropyrido[4,3-e][l,4]oxazepin-7(5H)-yl)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxamide 339 \ + co—O Jo o -' 4' o 2-(4-(1-(3-((4- (dodecyloxy)phenyl)sulfonyl) -6- (methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1 -ol 340 \ + co—O J.ooc-0'       ' o 2-(4-(l’-(3-((4- (dodecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)piperazin-1 -yl)ethan-1 -ol Ex. Structure Name 341 o O—co + \ 3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-l -yl)-[ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfinyl)quinoline 342 \ co—O 0' o 4-([l,4':r,4"-terpiperidin]-l"-yl)-3-((4-(dodecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline 343 o . -p O—co \ 1 "-(3 -((4-(dodecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4':r,4"-terpiperidin]-3-ol 344 o O—ui + \ 2-(4-(1 -(6-(methylsulfinyl)-3-((4-(tetradecyloxy)phenyl)sulfonyl)quinolin- 4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-l-ol 345 o O—to + \ 2-(4-(l'-(6-(methylsulfinyl)-3-((4-(tetradecyloxy)phenyl)sulfonyl)quinolin-4-yl)- [ 1,4'-bipiperidin] -4-yl)piperazin-1 -yl)ethan-l-ol Ex. Structure Name 346 o ,0 o o g o—+ \ 4-(4-(4-methylpiperazin-1 -yl)- [ 1,4’-bipiperidin]-l’-yl)-6-(methylsulfinyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinoline 347 o p Q —in \ 4-( [ 1,4’: 1 ’,4"-terpiperidin] -1 "-yl)-6-(methyl(X1-oxidanyl)-X3-sulfanyl)-3-((4-(tetradecyloxy)phenyl)sulfonyl)quinoline 348 o O Q — tn \ 1 "-(6-(methyllX1 -oxidanyl)- X3-sulfanyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinolin-4-yl)-[l,4’:r,4"-terpiperidin]-3-ol 349 ¢. 1 II Tl                               11 II [1 J J o [| 1 1-(1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)piperidin-4-yl)pyrrolidin-2-one 350 Ho^y-\ NX ¢, 1 II / S.      Jx .s. Ti ^1 ^1 11 Ti O J° LX / x — N    — 0 (1-(1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)piperidin-4-yl)pyrrolidin-2-yl)methanol 351 HO^___ XN--X '—N 0 2-(4-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-1,4-diazepan-l-yl)ethan-l-ol Ex. Structure Name 352 0 7-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-1 -isobutyldecahydropyrido[4,3-e][l,4]oxazepine 353 F3) HN 0A*° 0. 1 II / k xxdci / x^ 4-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-N-(2,2,2-trifluoroethyl)-l ,4-diazepane-l -sulfonamide 354 OH —X. '—hl 0 1 II _s.       A. YYj °Yk l-((4-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-1,4-diazepan-1 -yl)methyl)cyclopentan-1 -ol 355 0—| N-"\ N 0 1 II TtT SY1 VzA'0 / X / ^x 3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)-4-(4-(oxetan-3-yl)-l,4-diazepan-1 -yl)quinoline 356 Cl ^S N*^x N 0 1 II ^k YYy°Xl 2-(4-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-1,4-diazepan-l-yl)-6-chlorobenzo[d]thiazole 357 0 \A —N 0 1 H YYj kd l-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-4-methyl-1,4-diazepan-5-one Ex. Structure Name 358 N   0 1          H / k ii                ii>i 11 J J 0 II J 3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)-4-(4-(tetrahydro-2H-thiopyran-4-yl)-1,4-diazepan-1 -yl)quinoline 359 0 XN'^\ '—N   0 1          H _s.        .X ,s. 7f            n  ti J J o HI l\T 4-(4-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-1,4-diazepan- 1 -yl)tetrahydro-2H-thiopyran 1,1 -dioxide 360 0     ^NH 0 II                                    1 II \ X N       Tl              tT 11 II H IL JL J 0 IL JI 3-((4-methoxyphenyl)sulfonyl)-N-methyl-4-(methylamino)quinoline-6-carboxamide 361 ^o 0 O=oo=0 00-3 tn \ 1-(1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)piperidin-4-yl)pyrrolidin-2-one 362 \ + tn—O Sw rf- O -n 2-(4-(1 -(3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl) -6- (methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethanol 363 \ + cn—O ^0^00 O     -n 4-([l,4’:r,4"-terpiperidin]-l"-yl)-3-((4-(dodecyloxy)-3 -fluorophenyl) sulfonyl) -6-(methylsulfinyl)quinoline Ex. Structure Name 364 \ + Ln—Q Ln'                            O &    1 O     -n l"-(3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl) -6-(methylsulfinyl)quinolin-4-yl)-[l,4':r,4"-terpiperidin] -3 -ol 365 U-    O O—LO + \ 2-(4-(1 -(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethanol 366 u- O ..0 o—+ \ 4-([l,4':r,4"-terpiperidin]-l"-yl)-3-((3- fluoro-4-(tetradecyloxy)phenyl)sulfonyl)- 6-(methylsulfinyl)quinoline 367 u-     O .      .0 O                                .LO 1 O-Ll + \ l"-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4':r,4"-terpiperidin] -3 -ol 368 \ + in—O । $ O     -n 2-(4-(l’-(3-((4-(dodecyloxy)-3-fluorophenyl)sulfonyl) -6-(methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)piperazin-1 -yl)ethanol 369 u- O fi 1 O-<n + \ 2-(4-(l’-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)piperazin-1 -yl)ethanol - 150 - WO 2021 / 076886                                                 PCT / US2020 / 055979 Ex. Structure Name 375 o J 1 O—tn + \ l”-(6-(methylsulfinyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinolin-4-yl)-[ 1,4’: l’,4"-terpiperidin]-4-ol 376 HO' / ^ 0 N ?             0 XX J XX k. — N    — 2-(4-(1-(3-((4- (hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethanol 377 o O—to + 4-([l,4’:r,4"-terpiperidin]-l"-yl)-3-((4-(hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline 378 0 J XXX XXM l"-(3-((4- (hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinolin-4-yl)-[l,4’:r,4"-terpiperidin] -3 -ol 379 XN-"\ 0           0 II                        1 H \ N      7i                    11 Ti 1 I J ° I JI 3-((4-methoxyphenyl)sulfonyl)-N,N-dimethyl-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxamide Ex. Structure Name 380 0s o Ox / __7Z— I                \   / 1        / O—to + 2-(4-(1 -(6-(methylsulfinyl)-3-((4-(undecyloxy)phenyl)sulfonyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethanol 381 0 6 ?    ^T^Ox / ° XX X XX h. 4-( [ 1,4': 1 ’,4"-terpiperidin] -1 "-yl)-6- (methylsulfinyl)-3-((4- (undecyloxy)phenyl)sulfonyl)quinoline 382 Xo—O 0' o l"-(6-(methylsulfinyl)-3-((4- (undecyloxy)phenyl)sulfonyl)quinolin-4-yl) - [ 1,4': 1 ',4"-terpiperidin]-4-ol 383 0s o .         ,.0 o             V &-O<00 1 Q-to + l"-(6-(methylsulfinyl)-3-((4- (undecyloxy)phenyl)sulfonyl)quinolin-4-yl) - [ 1,4': 1 ',4"-terpiperidin]-3-ol Ex. Structure Name 384 o '--H O ,0 1 O—tn + 2-(4-((4-( [ 1,4': l',4"-terpiperidin] -1 "-yl)-6-(methylsulfinyl)quinolin-3 - yl) sulfonyl)phenoxy) -N,N-diethylethanamine 385 OH b 0 XX j XX h 2-(4-(l’-(3-((4- (hexadecyloxy)phenyl)sulfonyl) -6- (methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)piperazin-1 -yl)ethanol 386 ■bz>—Q । 0' o =0 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-l -yl)-[ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfinyl)quinoline Ex. Structure Name 387 0 0 J LX m 2-(4-(l’-(3-((3-fluoro-4-(hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinolin-4-yl)-[l,4’-bipiperidin] -4-yl)piperazin-1 -yl)ethanol 388 U- O .,0 1 O-co + 3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4’-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 389 U-     O .         ..0 O                               .CO 1 O—<O + l"-(3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinolin-4-yl)-[l,4':r,4"-terpiperidin] -3 -ol 390 \ + co-o । & O     -n .0 4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((3-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline Ex. Structure Name 391 0 6 ?       7 °s / ° +T T J T T w 3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin] - l'-yl)-6- (methylsulfinyl)quinoline 392 \z>—O I 0' O -n 3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methyl-1,4-diazepan-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfinyl)quinoline 393 z>—O I x° 0' O -n 4-( l'-(3-((3 -fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)morpholine 394 O I O   m 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline Ex. Structure Name 395 6 ?■                    f +Ta j Ta h ' '13 3-((2-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4’-bipiperidin] -l’-yl)-6-(methylsulfinyl)quinoline 396 1 0 0 ?             0 +TA J TA h N            °A 1                       13 F 3-((3,5 -difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)- [ 1,4’-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 397 0 0 x3txv TAnT TAqH 13 3-((2,3-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)- [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline Ex. Structure Name 398 1 0 ?   ^O\ / ° +XXX XX h 17 4-(4-(4-methylpiperazin-1 -yl)- [ 1,4’-bipiperidin]-l’-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline 399 6 6 ?       1 ^ / ° +XX X XX h N     — O\ 17 3-((3-fluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)- [ 1,4’-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 400 +X—o X \—X \—X \—X \s> \\ / / \ / \ / \__ / x° 0' O     -n 4-( l'-(3-((3 -fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin]-4-yl)thiomorpholine Ex. Structure Name 401 0 0 13 l-(4-(l'-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinolin-4-yl)-[l,4'- bipiperidin] -4-yl)piperazin-1 -yl)ethanone 402 6 0 0 Ta j xx h 13 3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfonyl)quinoline 403 0H N 0 / S\ZwLzSX^x XXJ XXh, 11 (S)-l"-(3-((4- (dodecyloxy)phenyl)sulfonyl)-6-((S)-methylsulfinyl)quinolin-4-yl)-[l,4':r,4"-terpiperidin] -3 -ol Ex. Structure Name N A (S)-l"-(3-((4- 404 AA A (dodecyloxy )phenyl)sulfonyl) -6 -((R) -methylsulfinyl)quinolin-4-yl)-[l,4':l',4"- 0 । Ar Ar h terpiperidin] -3 -ol ^oAk 11 ^l\A A (r).1"-(3-((4- 405 AA A (dodecyloxy)phenyl)sulfonyl)-6-((S)- methylsulfinyl)quinolin-4-yl)-[l,4':r,4"- + U7-HlO / 1 A / ) zx / AYa 1 7    7 H terpiperidin] -3 -ol ^A IL ^oAk 11 X\>0H ^lA A (r).1"-(3-((4- 406 ^A A (dodecyloxy )phenyl)sulfonyl) -6 -((R) -methylsulfinyl)quinolin-4-yl)-[l,4':r,4"- 0 ! ¥(^0 । Ar Ar h terpiperidin] -3 -ol ^A ^0Ak 11 HO^^ 0 N A (R)-2-(4-( l'-(3-((4-(dodecyloxy)-3- 407 0 fluorophenyl)sulfonyl) -6- (methylsulfinyl)quinolin-4-yl)-[l,4'- 0’ I tt Ar h .F bipiperidin] -4-yl)piperazin-1 -yl)ethanol H             J |l kAx 11 Ex. Structure Name 408 0 .  d 5             1 0. .0 / $                     F +T T J IT 11 (S)-2-(4-(l'-(3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl) -6- (methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)piperazin-1 -yl)ethanol 409 HO^^| 0 0 . 0 t            i o. / ° +lXT lX 13 (R)-2-(4-( 0-(3-((3 -fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)piperazin-1 -yl)ethanol 410 HO^^| 0 0 . 0 =            1 o. .0 .S.         A.               F 11;Tin 13 (S)-2-(4-(l'-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinolin-4-yl)-[l,4'-bipiperidin] -4-yl)piperazin-1 -yl)ethanol Ex. Structure Name 411 £ U-     O o—+ 3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl)-4-(4-(4- ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline 412 + CH —O %xm>: CO O    -n £ 3-((4-(dodecyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)quinoline 413 +\i—o \ & O     -n £ 3-((4-(dodecyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(methylsulfinyl)quinoline Ex. Structure Name 414 +\n—O co O    -n £ 4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((3-fluoro-4-(hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline 415 U-     O o—+ 3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfinyl)quinoline 416 u.     O o—to + 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4- (hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline Ex. Structure Name 417 +\o—Q 2   \-Z.   \— Z.   \-Z.   \z-- \\ / / \ / \ / \__ / cz> O    -n / / 3-((4-(dodecyloxy)-2,3- difluorophenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 418 LI-      O CO / \ / \ / \ / —    —\  —\ —\ O—to + 3-((4-(dodecyloxy)-2,3- difluorophenyl)sulfonyl)-4-(4-(4- ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline 419 +\n—O tr 0-0-0-( ' \^° co F° O     -n / / 3-((4-(dodecyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)quinoline Ex. Structure Name 420 LI-      O CO / \ / \ / \ / — Z\ / ——\   —\ O—to + 3-((4-(dodecyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 -yl) -6 -(methylsulfinyl)quinoline 421 LI-      O (Z) / \ / \ / \ / — Z\   —\ / Z—\ / Z —\ O—<-o + 3-((2,3-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline 422 £ LI-      O (Z) O—to + 3-((2,3-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfinyl)quinoline Ex. Structure Name 423 £ LI-      O CO / \ / \ / \ / — Z\ / ——\   —\ O—to + 3-((2,3-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl) -6 - (methylsulfinyl)quinoline 424 LI-      O (Z) / \ / \ / \ O—to + 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)- [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 425 LI-      O (Z) / \ / \ / \ / — Z\   —\ / Z—\ / Z —\ O—to + 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline Ex. Structure Name 426 LI-      O CO O—to + 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfinyl)quinoline 427 LI-      O CO / \ / \ / \ / — Z\   / —Z\ / Z—\ / Z —\ O—to + 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 - y 1) - 6 -(methylsulfinyl)quinoline 428 h\o—O Z  \—              Z — \\ / / \ / \ / \___ / x  \^° co ^x° O     -n 3-((4-(dodecyloxy)-3,5- difluorophenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)- [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline Ex. Structure Name 429 U-     O (Z) / \ / \ / \ / —   yz — / Z — / Z — / Z O—<-o + 3-((4-(dodecyloxy)-3,5- difluorophenyl)sulfonyl)-4-(4-(4- ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline 430 O ' \ / / ° (Z) ^-F° O -n £ 3-((4-(dodecyloxy)-3,5-difluorophenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)quinoline 431 +\n — O Z \— \—    Z — / Z / / / \ / \__ / \ / ' \^° (Z) ^-F° O     -n £ 3-((4-(dodecyloxy)-3,5-difluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(methylsulfinyl)quinoline Ex. Structure Name 432 +\o — O 2   \-Z.   \— Z.   \-Z.   \Z / / / \ / \ / \__ / CO O     -n 3-((3,5 -difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline 433 / / LI-      O CO O—to + 3-((3,5 -difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'- bipiperidin]-l'-yl)-6-(methylsulfinyl)quinoline 434 / / LL     O CO / \ / \ / \ / —    / —    —\   —\ O—to + 3-((3,5 -difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 - y 1) - 6 -(methylsulfinyl)quinoline Ex. Structure Name 435 +\o —O Z  \— Z  \-Z.  \-Z  \z- / / \ / \ / \__ / CO ^-F° O     -n / / 3-((3,5 -difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 436 / / LI-      O CO / \ / \ / \ / — Z\   —\ / Z—\ / Z—\ O—to + 3-((3,5 -difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline 437 +\ / i—o ' X^0 co O     -n 3-((3,5 -difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'- bipiperidin]-l'-yl)-6-(methylsulfinyl)quinoline Ex. Structure Name 438 +V>—o 2  \ Z.   \—Z.   \Z— /  \Z / / / \ / \__ / \ / ' \ / ° (Z) O     -n 3-((3,5 -difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl) -6 - (methylsulfinyl)quinoline 439 +\n — O 2   \— Z.   \ Z.   \— Z.   \z- \\ / / \ / \ / \__ / (Z> o 3-((4-(dodecyloxy)-2- fluorophenyl)sulfonyl)-4-(4-(4- methylpiperazin-1 -yl)- [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 440 — O 2   \— Z.   \— Z.   \— Z.   Z- / / \ / \ / \__ / x \ / / ° (Z) o 3-((4-(dodecyloxy)-2- fluorophenyl)sulfonyl)-4-(4-(4- ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline Ex. Structure Name 441 0 N 0 °' ! / V / SC / V *YTj YY « 3-((4-(dodecyloxy)-2-fluorophenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)quinoline 442 Y o CO / \ / \ / \ / —   / —    —\  —\ O—to + 3-((4-(dodecyloxy)-2-fluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(methylsulfinyl)quinoline 443 h\o—O z  \—   \— ~z.  \—    z — / / \ / \ / \__ / ' \ Y1 < / =^° o 4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((2-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline Ex. Structure Name 444 £ o CO O—to + 3-((2-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin] - l'-yl)-6- (methylsulfinyl)quinoline 445 o CO / \ / \ / \ / — Z\   / —Z\ / Z—\ / Z —\ O—to + 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((2-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 446 +\o—Q 2  \\z — \\ / / \ / \ / \__ / ' \^° to o 3-((2-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)- [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline Ex. Structure Name 447 o CO / \ / \ / \ / —    —\  —\   —\ O—to + 4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((2-fluoro-4-(hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline 448 o (Z) O—to + 3-((2-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfinyl)quinoline 449 £ o (Z) / \ / \ / \ / — Z\   / —Z\   —\ / Z—\ O—to + 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((2-fluoro-4-(hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline Ex. Structure Name 450 +\n —O O    -n 4-([l,4':r,4"-terpiperidin]-l"-yl)-3-((4-(dodecyloxy)-2,3- difluorophenyl)sulfonyl)-6-(methylsulfinyl)quinoline 451 +\o — O 2   \-Z.   \-Z.   \— Z.   \Z- / / / \ / \ / \__ / ' \^° co 0= o 3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 452 0 0 ¢1.0 *YYj Y1 w 3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfinyl)quinoline Ex. Structure Name 453 o .0 / \ / \ / \ / — —\ —\ —\ o—+ 4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinoline 454 +\z>—o tr O-O-OX ' \ / / ° co 0= o 4-(4-(4-isopropylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinoline 455 0C o (Z) / \ / \ / \ —Z   Z—(   Z—(   Z—C  Z + (R)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline Ex. Structure Name 456 + \n. iO 2  \\— z  \-Z   Z- / \ / \ / \__ / ' \ / / ° co 0° o =0 (S)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4 bipiperidin]-l'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline 457 +\n^O 2  \— Z  \-Z  \— Z  \Z- / \\   / / \   / \   / \__ / ' \^° co 0 o (R)-4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline 458 -i\n. iO 2  \ Z  \— Z  \ Z  \Z / / /  \ / \ / \ / x \ / / ° co 0 o =0 (S)-4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline Ex. Structure Name 459 3? o cn r\ /  \   /  \   /  \ □ ►tn + (R)-4-(4-(4-cyclopropylpiperazin-1 -yl)-[1,4'-bipiperidin]-r-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline 460 iO Z \\z <^1 / / \ / \ / \__ / ' \ / / ° ( / ) 0° o £ (S)-4-(4-(4-cyclopropylpiperazin-1 -yl)-[1,4'-bipiperidin]-r-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline 461 +^-0! \--( O \\\ 0° o =0 3-((4-(icosyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-l -yl) - [ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfinyl)quinoline Ex. Structure Name 462 O Z   \\-Z^ \-Z.   \z- / \\ / / \ / \ / \__ / ' \ / / ° cz> 0'° 0 =0 4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((4-(icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 463 Z   \-Z.   \-Z.   \— Z.   \Z- / / / \ / \ / \__ / ' \ / / ° (Z> 0 0 / / (R)-4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((4- (icosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline 464 +\n- lO Z   \-Z.   \— Z.   \-Z.   \z- \\   / / \   / \   / \__ / ' \ / / ° cz> 0 0 =0 (S)-4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((4- (icosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline Ex. Structure Name 465 0 0 0jj Y0 w 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-l -yl)-[ 1,4'-bipiperidin] - l'-yl)-6- (methylsulfinyl)quinoline 466 +\o—Q 2  \Z — w / / \ / \ / \__ / ' \ / / ° cz> 0 0 £ 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 467 +\o-*O 2   \---Z.   \---Z.   \— Z.   \Z-- / / /   \   / \   / \__ / x \ / ° co 0 0 ,2 (R)-3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)quinoline Ex. Structure Name 468 + cn- iO 2  \\\Z — w / / \ / \ / \__ / ' \ / / ° cz> 0° 0 / / (S)-3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin] - l'-yl)-6-(methylsulfinyl)quinoline 469 / / U-     O °%P / \ / \ / \ / — Z\ / Z—\ / Z—\ / Z—\ / Z + (R)-3-((4-(dodecyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline 470 / ° U-    O (Z) / \ / \ / \ / — Z\   / Z—\   / Z—\ / Z—\ / Z 01 + (S)-3-((4-(dodecyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1'-yl) -6 -(methylsulfinyl)quinoline Ex. Structure Name 471 z' \\-Z^ \-Z^ \Z- / / / \ / \ / \__ / >-----'          A------!          '------1 0'° O   n / / (R)-4-(4-(4-ethylpiperazin-1 -yl) - [ 1,4'-bipiperidin]-l'-yl)-3-((3-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 472 +    IO I Z \\Z / / / \ / \ / \__ / '---\ ZO '---      '---      '--- PT O    -n / / (S)-4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((3-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 473 / / o <Z) + (R)-3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)quinoline Ex. Structure Name 474 +^ / ). io (Z> 0 o (S)-3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl) - [ 1,4’-bipiperidin]-l’-yl)-6-(methylsulfinyl)quinoline 475 / ><O I Z \—Z \—Z \—Z  \z- / / \ / \ / \__ / Yf 0° O     -n £ (R)-3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)- [ 1,4’-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline 476 r>- lO I 2  \—Z \—Z \—Z  \z- / / \ / \ / \__ / 0'° O    -n =0 (S)-3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)- [ 1,4'-bipiperidin] -l'-yl)-6-(methylsulfinyl)quinoline Ex. Structure Name 477 1 .N. 0 'XXJ XXoa 17 (R)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4’-bipiperidin]-l'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline 478 + CO. lO z \—z. \—z. \—z.   z— / / \ / \ / \__ / x° 0' o (S)-4-(4-(4-methylpiperazin-1 -yl) - [ 1,4’-bipiperidin]-l’-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline 479 0 11 (R)-4-([ 1,4’: l',4"-terpiperidin] -1 "-yl)-3 -((4-(dodecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline Ex. Structure Name 480 + ( / >■ iO ^0=00 0° o & (S)-4-([ 1,4': l',4"-terpiperidin] -1 ”-yl)-3 -((4-(dodecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline 481 1 0 0, 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-l -yl)-[ 1,4'-bipiperidin]-l'-yl)-6- (methylthio)quinoline 482 1 0 0 d V i %*0 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-l -yl)-[ 1,4'-bipiperidin]-l'-yl)-6- (methylsulfonyl)quinoline Ex. Structure Name 483 o .0 / \ / \ / \ / — / ——\ —\ o—+ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(icosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline 484 0a o (Z) / \ / \ / \ / —    / ——\   —\ o—+ 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 - y 1) - 6 - (methylsulfinyl)quinoline 485 0= o ».0 <z> / \ / \ / \ / — / ——\ —\ o**^ + (R)-4-(4-(4-(l-ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-3 -((4-(icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline Ex. Structure Name 486 o .0 / \ / \ / \ / — / ——\ —\ Qi '< / 1 + (S)-4-(4-(4-(l-ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-3 -((4- (icosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline 487 o (Z) / \ / \ / \ / —    / ——\   —\ o*^ + (R)-3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl) -6 -(methylsulfinyl)quinoline 488 + iz>- iO 2 \\Z / \z \\ / / \ / \__ / \ / ' \ / / ° cn 0"° o =0 (S)-3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 - y 1) - 6 -(methylsulfinyl)quinoline Ex. Structure Name 489 + GH—Q 2  \\— Z  \-Z.  \Z- / / / \ / \ / \__ / GO 0° o 4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-6-(methylsulfinyl)-3-((4- (tetracosyloxy)phenyl)sulfonyl)quinoline 490 i5 o .0 GO / \ / \ / \ / ¾ / — / — —\ —\ O—go + 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl) -6 -(methylsulfinyl) -3 -((4- (tetracosyloxy)phenyl)sulfonyl)quinoline 491 +\o—O 2   \ Z.   \ Z.   \ Z.   \Z / / / \ / \ / \__ / ' \ / / ° GO 0 o 4-(4-(4-ethylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((4- (hexacosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline Ex. Structure Name 492 o -.0 cn / \ / \ / \ / — / — —\ —\ O—+ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(hexacosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline 493 +\o—Q Z \— ~Z.   \-~Z.   \-J.   \Z — / / \   /   \   /   \__ / ' \ / / ° cn / / o =0 3-((4-(icosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)-4-(4-(4-propylpiperazin-1 -yl)- [ 1,4'-bipiperidin] -1 '-yl)quinoline 494 0’ o ..0 Ln / \ / \ / \ O—Ln + 4-(4-(4-butylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((4-(icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline Ex. Structure Name 495 £ o ..0 CO / \ / \ / \ __z^— O—co + 3-((4-(docosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)-4-(4-(4-propylpiperazin-1 -yl) - [ 1,4'-bipiperidin] -1 '-yl)quinoline 496 h\o—O S—\\ / / \ / \ / \__ / ' \ / / ° cn / / o »0 4-(4-(4-butylpiperazin-1 -yl)- [ 1,4'-bipiperidin]-l'-yl)-3-((4-(docosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 497 \o 2   \\— -z.   \-Z.    Z-- / / \ / \ / \__ / x   \ / / ° co 0 o 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-l -yl)-[ 1,4'-bipiperidin]-l'-yl)-6- (methylthio)quinoline Ex. Structure Name 498 £ o (Z) / \ / \ / \ —Z   Z—(   Z—(   Z—C  Z °\ / ^(Z) oz \ 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-l -yl)-[ 1,4'-bipiperidin] - l'-yl)-6- (methylsulfonyl)quinoline 499 \n 2               Z- /  z— / / / \ / \__ / \ / ' \ / / ° co 0 o .0 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(hexadecyloxy)phenyl)sulfonyl) -6-(methylthio)quinoline 500 Z7-Q ! Z \\Z- /  \z- / / \ / \__ / \ / ' x / / ° cz> 0 o 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline Ex. Structure Name 501 £ o .0 / \ / \ / \ / — / — —\ —\ O\ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(hexadecyloxy)phenyl)sulfonyl) -6-methoxyquinoline 502 W0 n o Q7OOO7 GO 0° o £ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(hexadecyloxy)phenyl)sulfonyl) -6-(trifluoromethoxy)quinoline 503 \o 2  \Z- /  z— / \\ / 7 \ /   \__ / \ / ' \ / / ° GO 0° O     -n =0 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4- (hexadecyloxy)phenyl)sulfonyl) -6-(methylthio)quinoline Ex. Structure Name 504 £ U-    O / \ / \ / \ / —   / — —\ —\ 1 o—< / + 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4- (hexadecyloxy)phenyl)sulfonyl) -6-(methylsulfinyl)quinoline 505 LI-      O (Z) / \ / \ / \ / —    / ——\ —\ O\ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4-(hexadecyloxy)phenyl)sulfonyl) -6-methoxyquinoline 506 UJ1"1 n \ o co 0"° O -n £ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4- (hexadecyloxy)phenyl)sulfonyl) -6-(trifluoromethoxy)quinoline Ex. Structure Name 507 2  \Z- /  Z- / \\ / / \ / \__ / \ / ' \ / / ° cz> 0'° 0 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl) -6 -(methylthio) -3-((4-(octadecyloxy)phenyl)sulfonyl)quinoline 508 Q 0 f JJYl. w 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl) -6 -(methylsulfinyl) -3 -((4- (octadecyloxy)phenyl)sulfonyl)quinoline 509 ¥ 0 ¥ un / \ / \ / \ / —   / ——\  —\ O\ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl) -6 -methoxy-3 -((4-(octadecyloxy)phenyl)sulfonyl)quinoline Ex. Structure Name 510 0“ o o \ o LL? 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(octadecyloxy)phenyl)sulfonyl)-6-(trifluoromethoxy)quinoline 511 0“ LI-      O (Z) / \ / \ / \ / —    / ——\   —\ (Z) 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4-(octadecyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline 512 Z7-O ! 2 \\Z / \Z / \\ / 7   \ /   \__ /   \   / ' \ / / ° cz> 0° O     -n .0 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4-(octadecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline Ex. Structure Name 513 € U-    O / \ / \ / \ / —   / —    —\   —\ O\ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4-(octadecyloxy)phenyl)sulfonyl)-6-methoxyquinoline 514 £ u-    o KKK^-o o 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4-(octadecyloxy)phenyl)sulfonyl)-6-methoxyquinoline 515 o .0 / \ / \ / \ / — / — —\ —\ un 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(icosyloxy)phenyl)sulfonyl)-6- (methylthio)quinoline Ex. Structure Name 516 o .0 / \ / \ / \ / — / — —\ —\ 1 o—<X+ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(icosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline 517 0’ o (Z) / \ / \ / \ / —   / ——\   —\ O\ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(icosyloxy)phenyl)sulfonyl)-6- methoxyquinoline 518 UJ1"1 n \ o ^OO<D^ co 0"° o 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((4-(icosyloxy)phenyl)sulfonyl)-6- (trifluoromethoxy)quinoline Ex. Structure Name 519 2  \Z- /  Z- / \\   / / \ / \__ / \ / '    \ / / ° cz> 0 O     -n / / 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4- (icosyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline 520 / / LI-      O (Z) / \ / \ / \ / —   / ——\  —\ 10—<X+ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4- (icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 521 / / LI-      O / \ / \ / \ / r^ / —    / —    —\   —\ O\ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4-(icosyloxy)phenyl)sulfonyl)-6- methoxyquinoline Ex. Structure Name 522 UJ11 n \ o co 0'° O -n £ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin- 1-yl)-3-((3 -fluoro-4-(icosyloxy)phenyl)sulfonyl)-6- (trifluoromethoxy)quinoline 523 £ o (Z) / \ / \ / \ / —    / ——\   —\ CO 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl) -6 - (methylthio)quinoline 524 Z7-O ! 2  \\Z / \Z / \\ / 7   \ /   \__ /   \   / ' \ / / ° co 0 o =0 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 - y 1) - 6 - (methylsulfinyl)quinoline Ex. Structure Name 525 o .0 / \ / \ / \ / — / — —\ —\ O\ 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl) -6 -methoxy quinoline 526 W0 n o Q7OOO7 GO 0° o 0 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 - y 1) - 6 - (trifluoromethoxy)quinoline 527 \o 2  \Z- /  z— / \\ / 7 \ /   \__ / \ / ' \ / / ° GO 0' O     -n =0 3-((4-(docosyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(methylthio)quinoline Ex. Structure Name 528 2 \z— / z \\ / / \ / \__ / \ / ' \ / / ° co 0“ O     -n =0 3-((4-(docosyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 -yl) -6 -(methylsulfinyl)quinoline 529 / / LI-      O (Z) / \ / \ / \ / —   / ——\ —\ O\ 3-((4-(docosyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 -yl) -6 -methoxy quinoline 530 UJ1"1 n \ O co 0"° O -n 3-((4-(docosyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(trifluoromethoxy)quinoline Ex. Structure Name 531 Q 0 6 ? °X / ° .0.                            _F F3C XXCX XX m F 3 -((4-(docosyloxy) -3,5-difluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 -yl) -6 -(trifluoromethoxy)quinoline 532 (J?1 n \ O \ & co _ O    -n 3-((4-(docosyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(trifluoromethoxy)quinoline 533 0 I F3C XXj lX m 21 3-((4-(docosyloxy)-2-fluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(trifluoromethoxy)quinoline Ex. Structure Name 534 Q 0 d ? Ox / ° .CL            2s'       _F F3C XXj XX m F 3-((3,5 -difluoro-4-(icosyloxy)phenyl)sulfonyl)-4-(4-(4-( 1 -ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 -yl) -6 -(trifluoromethoxy)quinoline 535 (J?1 n \ O \ & co _ O    -n £ 3-((2,3-difluoro-4-(icosyloxy)phenyl)sulfonyl)-4-(4-(4-( 1 -ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(trifluoromethoxy)quinoline 536 n O o 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((2-fluoro-4-(icosyloxy)phenyl)sulfonyl)-6-(trifluoromethoxy)quinoline Ex. Structure Name 537 Q 0 d ? Ox / ° .CL            2s'       _F F3C XXj XX m F 3-((3,5 -difluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 -yl) -6 - (trifluoromethoxy)quinoline 538 (J?1 n \ O %OC-<3^ CO 0*0 O   n £ 3-((2,3-difluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 - y 1) - 6 - (trifluoromethoxy)quinoline 539 n O ■^-ao-c-7 ^*o o £ 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((2-fluoro-4-(octadecyloxy)phenyl)sulfonyl)-6-(trifluoromethoxy)quinoline Ex. Structure Name 540 Q 0 6 ? Ox / ° .CL            2s'       _F F3C XXj XX m F 3-((3,5 -difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 -yl) -6 - (trifluoromethoxy)quinoline 541 (J?1 n \ O \ co O   n 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 - y 1) - 6 - (trifluoromethoxy)quinoline 542 n \ O o 4-(4-(4-( 1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3 -((2-fluoro-4-(hexadecyloxy)phenyl)sulfonyl) -6-(trifluoromethoxy)quinoline Ex. Structure Name 543 n \ O -n      co o £ 3-((2,6-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 -yl) -6 - (trifluoromethoxy)quinoline 544 o o \ o cn 3-((2,6-difluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 - y 1) - 6 - (trifluoromethoxy)quinoline 545 o o o cn 3-((2,6-difluoro-4-(icosyloxy)phenyl)sulfonyl)-4-(4-(4-( 1 -ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(trifluoromethoxy)quinoline Ex. Structure Name 546 n \ O Qs-OC-C--7 -n      GO o £ 3-((4-(docosyloxy)-2,6-difluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 -yl) -6 -(trifluoromethoxy)quinoline 547 Q |O„O 1 F3C XXCX lX m Y^O<^ F 3-((2,5-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 - y 1) - 6 - (trifluoromethoxy)quinoline 548 0 Xo 1 A.      A. F3C XXlX lX m F 3-((2,5-difluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 - y 1) - 6 -(trifluoromethoxy)quinoline Ex. Structure Name 549 u?1 n o cn o £ 3-((2,5-difluoro-4-(icosyloxy)phenyl)sulfonyl)-4-(4-(4-( 1 -ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 -yl) -6 -(trifluoromethoxy)quinoline 550 Q 0 0 . ? 0N / 0  1 A.     A. F3C XXj Yjl m F 3-((4-(docosyloxy)-2,5-difluorophenyl)sulfonyl)-4-(4-(4-(l-ethylpiperidin-4-yl)piper azin-1 -yl)piperidin-1 - y 1) - 6 -(trifluoromethoxy)quinoline

[0216] In certain embodiments, provided is a salt of a compound of this disclosure. In certain embodiments, the salt is salt of a compound of this disclosure formed with hydrochloric acid, hydrochloric acid, phosphoric acid, methanesulfonic acid (mesylate salt), malic acid, malonic acid, maleic acid, fumaric acid, tartaric acid, citric acid, acetic acid, or oxalic acid. In certain embodiments, the salt is a salt of a compound of this disclosure formed with methanesulfonic acid (mesylate salt). In certain embodiments, the salt is a salt of a compound of this disclosure formed with oxalic acid. In any of these embodiments, the salt is a salt of a compound of this disclosure formed with oxalic acid dihydrate. In any of these embodiments, the salt is a tris(oxalic acid dihydrate) salt. 3. Methods

[0217] The methods described herein may be applied to cell populations in vivo or ex vivo. “In vivo” means within a living individual, as within an animal or human. In this context, the methods described herein may be used therapeutically in an individual. “Ex vivo” means outside of a living individual. Examples of ex vivo cell populations include in vitro cell cultures and biological samples including fluid or tissue samples obtained from individuals. Such samples may be obtained by methods well known in the art. Exemplary biological fluid samples include blood, cerebrospinal fluid, urine and saliva. In this context, the compounds and compositions described herein may be used for a variety of purposes, including therapeutic and experimental purposes. For example, the compounds and compositions described herein may be used ex vivo to determine the optimal schedule and / or dosing of administration of a compound of the present disclosure for a given indication, cell type, individual, and other parameters. Information gleaned from such use may be used for experimental purposes or in the clinic to set protocols for in vivo treatment. Other ex vivo uses for which the compounds and compositions described herein may be suited are described below or will become apparent to those skilled in the art.

[0218] The present disclosure provides compounds and compositions for treating pathogenic blood vessel disorders such as diabetic retinopathy, age-related macular degeneration (AMD), retinopathy of prematurity, or cancer. The treatment can be through killing tumor blood vessels. In some embodiments, a tumor patient that can be suitably treated by the present technology expresses a plexin domain-containing protein (e.g., PLXDC1 or PLXDC2). The expression may be on a tumor blood epithelial cell.

[0219] As noted, the present technology not only can inhibit growth of new tumor blood vessels, but can also kill existing tumor blood vessels, thereby treating the tumor. In some embodiments, therefore, a tumor patient that can benefit from the present treatment is one that has a tumor that has undergone tumor angiogenesis. In some embodiments, the tumor comprises a vascularized tumor. In some embodiments, the tumor being treat has a diameter that is greater than about 0.1, 0.2, 0.3, 0.4, 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 7, 8, 9 or 10 cm (or any derivable range therein). In some embodiments, the tumor already contains tumor blood vessels.

[0220] In some embodiments, the tumor does not have a known tumor surface marker as target for immunotherapy. In some embodiments, the tumor does not contain a mutant gene that serves as a target for tumor therapy. In some embodiments, the therapy of the present disclosure does not include inducing antibody-dependent cell-mediated cytotoxicity (ADCC). In some embodiments, a therapeutic agent of the present disclosure does not induce ADCC.

[0221] In some embodiments, the patient suffers from a cancer such as, polycythemia ver a, lymphomas (e.g., Hodgkin's disease and non-Hodgkin's disease), multiple myeloma, Waldenstrom's macroglobulinemia, heavy chain disease, and solid tumors including, but not limited to, sarcomas and carcinomas such as fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyo sarcoma, colon carcinoma, pancreatic cancer, breast cancer, thyroid cancer, endometrial cancer, melanoma, prostate cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilm's tumor, cervical cancer, testicular tumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, menangioma, melanoma, neuroblastoma and retinoblastoma.

[0222] In some embodiments, the compounds and compositions described herein may be used to treat any cancerous or pre-cancerous tumor, such as a solid tumor. Cancers that may be treated by compounds and compositions provided herein include, but are not limited to, cancer cells from the bladder, blood, bone, bone marrow, brain, breast, colon, esophagus, gastrointestine, gum, head, kidney, liver, lung, nasopharynx, neck, ovary, prostate, skin, stomach, testis, tongue, or uterus. In addition, the cancer may specifically be of the following histological type, though it is not limited to these: neoplasm, malignant; carcinoma; carcinoma, undifferentiated; giant and spindle cell carcinoma; small cell carcinoma; papillary carcinoma; squamous cell carcinoma; lymphoepithelial carcinoma; basal cell carcinoma; pilomatrix carcinoma; transitional cell carcinoma; papillary transitional cell carcinoma; adenocarcinoma; gastrinoma, malignant; cholangiocarcinoma; hepatocellular carcinoma; combined hepatocellular carcinoma and cholangiocarcinoma; trabecular adenocarcinoma; adenoid cystic carcinoma; adenocarcinoma in adenomatous polyp; adenocarcinoma, familial polyposis coli; solid carcinoma; carcinoid tumor, malignant; branchiolo-alveolar adenocarcinoma; papillary adenocarcinoma; chromophobe carcinoma; acidophil carcinoma; oxyphilic adenocarcinoma; basophil carcinoma; clear cell adenocarcinoma; granular cell carcinoma; follicular adenocarcinoma; papillary and follicular adenocarcinoma; nonencapsulating sclerosing carcinoma; adrenal cortical carcinoma; endometrioid carcinoma; skin appendage carcinoma; apocrine adenocarcinoma; sebaceous adenocarcinoma; ceruminous adenocarcinoma; mucoepidermoid carcinoma; cystadenocarcinoma; papillary cystadenocarcinoma; papillary serous cystadenocarcinoma; mucinous cystadenocarcinoma; mucinous adenocarcinoma; signet ring cell carcinoma; infiltrating duct carcinoma; medullary carcinoma; lobular carcinoma; inflammatory carcinoma; mammary paget's disease; acinar cell carcinoma; adenosquamous carcinoma; adenocarcinoma w / squamous metaplasia; malignant thymoma; malignant ovarian stromal tumor; malignant thecoma; malignant granulosa cell tumor; and malignant roblastoma; sertoli cell carcinoma; malignant leydig cell tumor; malignant lipid cell tumor; malignant paraganglioma; malignant extra-mammary paraganglioma; pheochromocytoma; glomangiosarcoma; malignant melanoma; amelanotic melanoma; superficial spreading melanoma; malignant melanoma in giant pigmented nevus; epithelioid cell melanoma; malignant blue nevus; sarcoma; fibrosarcoma; malignant fibrous histiocytoma; myxosarcoma; liposarcoma; leiomyosarcoma; rhabdomyosarcoma; embryonal rhabdomyosarcoma; alveolar rhabdomyosarcoma; stromal sarcoma; malignant mixed tumor; mullerian mixed tumor; nephroblastoma; hepatoblastoma; carcinosarcoma; malignant mesenchymoma; malignant brenner tumor; malignant phyllodes tumor; synovial sarcoma; malignant mesothelioma; dysgerminoma; embryonal carcinoma; malignant teratoma; malignant struma ovarii; choriocarcinoma; malignant mesonephroma; hemangiosarcoma; malignant hemangioendothelioma; kaposi's sarcoma; malignant hemangiopericytoma; lymphangiosarcoma; osteosarcoma; juxtacortical osteosarcoma; chondrosarcoma; malignant chondroblastoma; mesenchymal chondrosarcoma; giant cell tumor of bone; ewing's sarcoma; malignant odontogenic tumor; ameloblastic odontosarcoma; malignant ameloblastoma; ameloblastic fibrosarcoma; malignant pinealoma; chordoma; malignant glioma; ependymoma; astrocytoma; protoplasmic astrocytoma; fibrillary astrocytoma; astroblastoma; glioblastoma; oligodendroglioma; oligodendroblastoma; primitive neuroectodermal; cerebellar sarcoma; ganglioneuroblastoma; neuroblastoma; retinoblastoma; olfactory neurogenic tumor; malignant meningioma; neurofibrosarcoma; malignant neurilemmoma; malignant granular cell tumor; malignant lymphoma; Hodgkin's disease; Hodgkin's lymphoma; paragranuloma; small lymphocytic malignant lymphoma; diffuse large cell malignant lymphoma; follicular malignant lymphoma; mycosis fungoides; other specified non-Hodgkin's lymphomas; malignant histiocytosis; multiple myeloma; mast cell sarcoma or immunoproliferative small intestinal disease.

[0223] In some embodiments, the subject has cancer, optionally comprising a solid tumor. An agent disclosed herein may be administered locally to the tumor. In some embodiments, the tumor is an adenocarcinoma, an adrenal tumor, an anal tumor, a bile duct tumor, a bladder tumor, a bone tumor, a blood born tumor, a brain / CNS tumor, a breast tumor, a cervical tumor, a colorectal tumor, an endometrial tumor, an esophageal tumor, an Ewing tumor, an eye tumor, a gallbladder tumor, a gastrointestinal, a kidney tumor, a laryngeal or hypopharyngreal tumor, a liver tumor, a lung tumor, a mesothelioma tumor, a multiple myeloma tumor, a muscle tumor, a nasopharyngeal tumor, a neuroblastoma, an oral tumor, an osteosarcoma, an ovarian tumor, a pancreatic tumor, a penile tumor, a pituitary tumor, a primary tumor, a prostate tumor, a retinoblastoma, a Rhabdomyosarcoma, a salivary gland tumor, a soft tissue sarcoma, a melanoma, a metastatic tumor, a basal cell carcinoma, a Merkel cell tumor, a testicular tumor, a thymus tumor, a thyroid tumor, a uterine tumor, a vaginal tumor, a vulvar tumor, or a Wilms tumor. In some embodiments, a compound and / or composition described herein may be administered parenterally, at or near the site of a tumor, or distant from the site of the tumor.

[0224] Actual dosage levels of the active ingredients in the pharmaceutical compositions may be varied so as to obtain an amount of the active ingredient which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient.

[0225] The selected dosage level will depend upon a variety of factors including the activity of the particular agent employed, the route of administration, the time of administration, the rate of excretion or metabolism of the particular compound being employed, the duration of the treatment, other drugs, compounds and / or materials used in combination with the particular compound employed, the age, sex, weight, condition, general health and prior medical history of the patient being treated, and like factors well known in the medical arts.

[0226] A physician or veterinarian having ordinary skill in the art can readily determine and prescribe the effective amount of the pharmaceutical composition required. For example, the physician or veterinarian could prescribe and / or administer doses of the compounds employed in the pharmaceutical composition at levels lower than that required in order to achieve the desired therapeutic effect and gradually increase the dosage until the desired effect is achieved.

[0227] The administration of one or more compounds as described herein may result in at least a 10% decrease (e.g., at least 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90% or even 100% decrease in one or more symptoms of a disease or condition, such as a decrease in tumor size.

[0228] Compounds described herein can be used in methods for agonizing Pigment-Epithelium-Derived Factor (PEDF) receptors. Compounds described herein can also be used in methods for inhibiting angiogenesis.

[0229] The PEDF receptors have been identified as two homologous membrane proteins called plexin domain containing 1 (PLXDC1) and plexin domain containing 2 (PLXDC2). They belong to a new type of cell-surface receptors and are the only proteins that are known to confer cell-surface binding to PEDF and to transduce PEDF signal into the target cells. Consistent with the ability of PEDF to suppress pathogenic angiogenesis in blinding diseases and in cancer without affecting healthy blood vessels, the PEDF receptors are highly expressed in pathogenic blood vessels in many diseases, including tumor blood vessels and diabetic retinopathy. The PEDF receptors are not detected in healthy blood vessels. One of the PEDF receptors (TEM7, PLXDC1) was well studied in the past as a tumor endothelial marker that is enriched in tumor blood vessels of diverse types of human cancer including colon, liver, lung, breast, pancreatic, brain, bladder, ovarian, kidney, esophagus, gastric and endometrial cancer and Kaposi sarcoma, liposarcoma and synovial sarcoma. In blinding diseases, PEDF receptor TEM7 (PLXDC1) is highly expressed in pathogenic blood vessels of diabetic retinopathy, retinal occlusive vascular disease, retinopathy of prematurity, and choroidal neovascularization (pathogenic angiogenesis in AMD). This is consistent with the role of PEDF in suppressing pathogenic angiogenesis in these diseases without affecting healthy blood vessels.

[0230] The compounds and methods described herein can therefore be used in treating disease mediated by PEDF receptors or associated with angiogenesis, such as cancer, retinal occlusive vascular disease, retinopathy of prematurity, diabetic retinopathy, and age-related macular degeneration.

[0231] In certain embodiments, provided herein are methods for agonizing Pigment-Epithelium-Derived Factor (PEDF) receptors in a patient in need thereof comprising administering to said patient a therapeutically effective amount of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof.

[0232] In certain embodiments, provided herein are methods for inhibiting angiogenesis in a patient in need thereof comprising administering to said patient a therapeutically effective amount of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof. In certain embodiments, the angiogenesis is pathogenic angiogenesis.

[0233] Also provided herein are methods for treating a disease or disorder mediated by PEDF receptors in a patient in need thereof comprising administering to said patient a therapeutically effective amount of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof.

[0234] Also provided herein are methods for treating a disease or disorder associated with angiogenesis in a patient in need thereof comprising administering to said patient a therapeutically effective amount of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof.

[0235] Also provided herein are methods for treating a disease or disorder selected from a cancer, retinal occlusive vascular disease, retinopathy of prematurity, diabetic retinopathy, and age-related macular degeneration comprising administering to said patient a therapeutically effective amount of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof. In certain embodiments, the cancer is selected from colon, liver, lung, breast, pancreatic, brain, bladder, ovarian, kidney, esophagus, gastric and endometrial cancer and Kaposi sarcoma, liposarcoma and synovial sarcoma. In certain embodiments, the disease is a blinding disease. In certain embodiments, the disease is diabetic retinopathy, retinal occlusive vascular disease, retinopathy of prematurity, or choroidal neovascularization (pathogenic angiogenesis in AMD).

[0236] In certain embodiments, provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in a method for agonizing Pigment-Epithelium-Derived Factor (PEDF) receptors in a patient in need thereof comprising administering to said patient a therapeutically effective amount of the compound, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof.

[0237] In certain embodiments, provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in a method for inhibiting angiogenesis in a patient in need thereof comprising administering to said patient a therapeutically effective amount of the compound, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof. In certain embodiments, the angiogenesis is pathogenic angiogenesis.

[0238] Also provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in a method for treating a disease or disorder mediated by PEDF receptors in a patient in need thereof comprising administering to said patient a therapeutically effective amount of the compound, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof.

[0239] Also provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in a method for treating a disease or disorder associated with angiogenesis in a patient in need thereof comprising administering to said patient a therapeutically effective amount of the compound, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof.

[0240] Also provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in a method for treating a disease or disorder selected from a cancer, retinal occlusive vascular disease, retinopathy of prematurity, diabetic retinopathy, and age-related macular degeneration comprising administering to said patient a therapeutically effective amount of the compound, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof. In certain embodiments, the cancer is selected from colon, liver, lung, breast, pancreatic, brain, bladder, ovarian, kidney, esophagus, gastric and endometrial cancer and Kaposi sarcoma, liposarcoma and synovial sarcoma. In certain embodiments, the disease is a blinding disease. In certain embodiments, the disease is diabetic retinopathy, retinal occlusive vascular disease, retinopathy of prematurity, or choroidal neovascularization (pathogenic angiogenesis in AMD).

[0241] In certain embodiments, provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in the manufacture of a medicament for agonizing PigmentEpithelium-Derived Factor (PEDF) receptors in a patient in need thereof.

[0242] In certain embodiments, provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in the manufacture of a medicament for inhibiting angiogenesis in a patient in need thereof. In certain embodiments, the angiogenesis is pathogenic angiogenesis.

[0243] Also provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in the manufacture of a medicament for treating a disease or disorder mediated by PEDF receptors in a patient in need thereof.

[0244] Also provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in the manufacture of a medicament for treating a disease or disorder associated with angiogenesis in a patient in need thereof.

[0245] Also provided herein is use of a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in the manufacture of a medicament for treating a disease or disorder selected from a cancer, retinal occlusive vascular disease, retinopathy of prematurity, diabetic retinopathy, and age-related macular degeneration. In certain embodiments, the cancer is selected from colon, liver, lung, breast, pancreatic, brain, bladder, ovarian, kidney, esophagus, gastric and endometrial cancer and Kaposi sarcoma, liposarcoma and synovial sarcoma. In certain embodiments, the disease is a blinding disease. In certain embodiments, the disease is diabetic retinopathy, retinal occlusive vascular disease, retinopathy of prematurity, or choroidal neovascularization (pathogenic angiogenesis in AMD). 4. Kits

[0246] Provided herein are also kits that include a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, and suitable packaging. In certain embodiments, a kit further includes instructions for use. In one aspect, a kit includes a compound of the disclosure, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, and a label and / or instructions for use of the compounds in the treatment of the indications, including the diseases or conditions, described herein.

[0247] Provided herein are also articles of manufacture that include a compound described herein or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof in a suitable container. The container may be a vial, jar, ampoule, preloaded syringe and intravenous bag. 5. Pharmaceutical Compositions and Modes of Administration

[0248] Compounds provided herein are usually administered in the form of pharmaceutical compositions. Thus, provided herein are also pharmaceutical compositions that contain one or more of the compounds described herein or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof (collectively and individually, the “active ingredient”) and one or more pharmaceutically acceptable vehicles selected from carriers, adjuvants and excipients. Suitable pharmaceutically acceptable vehicles may include, for example, inert solid diluents and fillers, diluents, including sterile aqueous solution and various organic solvents, permeation enhancers, solubilizers and adjuvants. Such compositions are prepared in a manner well known in the pharmaceutical art. See, e.g., Remington’s Pharmaceutical Sciences, Mace Publishing Co., Philadelphia, Pa. 17th Ed. (1985); and Modern Pharmaceutics, Marcel Dekker, Inc. 3rd Ed. (G.S. Banker & C.T. Rhodes, Eds.). About 0.1 % to about 90 % of the total weight of the composition may be the active ingredient.

[0249] The therapeutic agents of the disclosure may be administered by the same route of administration or by different routes of administration. In some embodiments, the cancer therapy is administered intravenously, intramuscularly, subcutaneously, topically, orally, transdermally, intraperitoneally, intraorbitally, by implantation, by inhalation, intrathecally, intraventricularly, or intranasally. In some embodiments, the antibiotic is administered intravenously, intramuscularly, subcutaneously, topically, orally, transdermally, intraperitoneally, intraorbitally, by implantation, by inhalation, intrathecally, intraventricularly, or intranasally. The appropriate dosage may be determined based on the type of disease to be treated, severity and course of the disease, the clinical condition of the individual, the individual's clinical history and response to the treatment, and the discretion of the attending physician.

[0250] One mode for administration is parenteral, for example, by injection. The forms in which the pharmaceutical compositions described herein may be incorporated for administration by injection include, for example, aqueous or oil suspensions, or emulsions, with sesame oil, corn oil, cottonseed oil, or peanut oil, as well as elixirs, mannitol, dextrose, or a sterile aqueous solution, and similar pharmaceutical vehicles.

[0251] Oral administration may be another route for administration of the compounds described herein. Administration may be via, for example, capsule or enteric coated tablets. In making the pharmaceutical compositions that include at least one compound described herein or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, the active ingredient is usually diluted by an excipient and / or enclosed within such a carrier that can be in the form of a capsule, sachet, paper or other container. When the excipient serves as a diluent, it can be in the form of a solid, semi-solid, or liquid material, which acts as a vehicle, carrier or medium for the active ingredient. Thus, the compositions can be in the form of tablets, pills, powders, lozenges, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, aerosols (as a solid or in a liquid medium), ointments containing, for example, up to 10% by weight of the active compound, soft and hard gelatin capsules, sterile injectable solutions, and sterile packaged powders.

[0252] Some examples of suitable excipients include, e.g., lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, calcium phosphate, alginates, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, sterile water, syrup and methyl cellulose. The formulations can additionally include lubricating agents such as talc, magnesium stearate and mineral oil; wetting agents; emulsifying and suspending agents; preserving agents such as methyl and propylhydroxy-benzoates; sweetening agents; and flavoring agents.

[0253] The compositions that include at least one compound described herein or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof can be formulated so as to provide quick, sustained or delayed release of the active ingredient after administration to the subject by employing procedures known in the art. Controlled release drug delivery systems for oral administration include osmotic pump systems and dissolutional systems containing polymer-coated reservoirs or drug-polymer matrix formulations. Another formulation for use in the methods disclosed herein employ transdermal delivery devices (“patches”). Such transdermal patches may be used to provide continuous or discontinuous infusion of the compounds described herein in controlled amounts. The construction and use of transdermal patches for the delivery of pharmaceutical agents is well known in the art. Such patches may be constructed for continuous, pulsatile, or on demand delivery of pharmaceutical agents.

[0254] For preparing solid compositions such as tablets, the active ingredient may be mixed with a pharmaceutical excipient to form a solid preformulation composition containing a homogeneous mixture of a compound described herein or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof. When referring to these preformulation compositions as homogeneous, the active ingredient may be dispersed evenly throughout the composition so that the composition may be readily subdivided into equally effective unit dosage forms such as tablets, pills and capsules.

[0255] The tablets or pills of the compounds described herein may be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action, or to protect from the acid conditions of the stomach. For example, the tablet or pill can include an inner dosage and an outer dosage component, the latter being in the form of an envelope over the former. The two components can be separated by an enteric layer that serves to resist disintegration in the stomach and permit the inner component to pass intact into the duodenum or to be delayed in release. A variety of materials can be used for such enteric layers or coatings, such materials including a number of polymeric acids and mixtures of polymeric acids with such materials as shellac, cetyl alcohol and cellulose acetate.

[0256] Compositions for inhalation or insufflation may include solutions and suspensions in pharmaceutically acceptable, aqueous or organic solvents, or mixtures thereof, and powders. The liquid or solid compositions may contain suitable pharmaceutically acceptable excipients as described herein. In some embodiments, the compositions are administered by the oral route, or by the nasal respiratory route for rapid delivery to blood / blood vessels via the lungs, for local and / or systemic effect. In other embodiments, compositions in pharmaceutically acceptable solvents may be nebulized by use of inert gases. Nebulized solutions may be inhaled directly from the nebulizing device or the nebulizing device may be attached to a facemask tent, or intermittent positive pressure breathing machine. Solution, suspension, or powder compositions may be administered, preferably orally or nasally, from devices that deliver the formulation in an appropriate manner. 6. Dosing

[0257] The specific dose level of a compound of the present application for any particular subject will depend upon a variety of factors including the activity of the specific compound employed, the age, body weight, general health, sex, diet, time of administration, route of administration, and rate of excretion, drug combination and the severity of the particular disease in the subject undergoing therapy.

[0258] The treatments may include various “unit doses.” Unit dose is defined as containing a predetermined-quantity of the therapeutic composition. The quantity to be administered, and the particular route and formulation, is within the skill of determination of those in the clinical arts. A unit dose need not be administered as a single injection but may comprise continuous infusion over a set period of time. In some embodiments, a unit dose comprises a single administrable dose.

[0259] The quantity to be administered, both according to number of treatments and unit dose, depends on the treatment effect desired. An effective dose is understood to refer to an amount necessary to achieve a particular effect. In the practice in certain embodiments, it is contemplated that doses in the range from 10 mg / kg to 200 mg / kg can affect the protective capability of these agents. Thus, it is contemplated that doses include doses of about 0.1, 0.5, 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195, and 200, 300, 400, 500, 1000 pg / kg, mg / kg, pg / day, or mg / day or any range derivable therein. Furthermore, such doses can be administered at multiple times during a day, and / or on multiple days, weeks, or months.

[0260] In certain embodiments, the effective dose of the pharmaceutical composition is one which can provide a blood level of about 1 pM to 150 pM. In another embodiment, the effective dose provides a blood level of about 4 pM to 100 pM.; or about 1 pM to 100 pM; or about 1 pM to 50 pM; or about 1 pM to 40 pM; or about 1 pM to 30 pM; or about 1 pM to 20 pM; or about 1 pM to 10 pM; or about 10 pM to 150 pM; or about 10 pM to 100 pM; or about 10 pM to 50 pM; or about 25 pM to 150 pM; or about 25 pM to 100 pM; or about 25 pM to 50 pM; or about 50 pM to 150 pM; or about 50 pM to 100 pM (or any range derivable therein). In other embodiments, the dose can provide the following blood level of the agent that results from a therapeutic agent being administered to a subject: about, at least about, or at most about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, or 100 pM or any range derivable therein. In certain embodiments, the therapeutic agent that is administered to a subject is metabolized in the body to a metabolized therapeutic agent, in which case the blood levels may refer to the amount of that agent. Alternatively, to the extent the therapeutic agent is not metabolized by a subject, the blood levels discussed herein may refer to the unmetabolized therapeutic agent.

[0261] For example, a dosage may be expressed as a number of milligrams of a compound described herein per kilogram of the subject’s body weight (mg / kg). Dosages of between about 0.1 and 150 mg / kg may be appropriate. In some embodiments, about 0.1 and 100 mg / kg may be appropriate. In other embodiments a dosage of between 0.5 and 60 mg / kg may be appropriate. In some embodiments, a dosage of from about 0.0001 to about 100 mg per kg of body weight per day, from about 0.001 to about 50 mg of compound per kg of body weight, or from about 0.01 to about 10 mg of compound per kg of body weight may be appropriate. Normalizing according to the subject’s body weight is particularly useful when adjusting dosages between subjects of widely disparate size, such as occurs when using the drug in both children and adult humans or when converting an effective dosage in a non-human subject such as dog to a dosage suitable for a human subject. 7. ...

Claims

1. A method for treating a pathogenic blood vessel-related disorder in a subject in need thereof,comprising administering to the subject an effective amount of a compound of Formula (I):(I)or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof;whereinn is 0, 1, 2, 3 or 4;R1 is selected from optionally substituted amino, optionally substituted aryl, optionally substituted cycloalkyl, optionally substituted heterocyclyl, and optionally substituted heteroaryl;R2 is selected from H, halo, alkyl, alkenyl, alkynyl, -OH, alkoxy, alkenoxy, alkynoxy, -CN, -NO2, alkylthio, sulfoxido, sulfonyl, and amino;R5, R7 and R8 are each independently selected from H, halo, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, and amido;R6 is selected from H, halo, alkyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester,-CN, -NO2, amino, amido, sulfinamido, sulfonamido, optionally substituted heterocyclyl, optionally substituted heteroaryl, poly(ethylene glycol), and methoxypoly(ethylene glycol), orR6 and R7 together with atoms to which they are attached form an optionally substituted cycloalkyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl; andeach R9 is independently selected from halo, alkyl, -OH, alkoxy, -CN, and amino.

2. A method of inhibiting angiogenesis in a subject in need thereof, comprising administering tothe subject an effective amount of a compound of Formula (I):(I),or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof;wherein2020365108   27 Aug 2026n is 0, 1, 2, 3 or 4;R1 is selected from optionally substituted amino, optionally substituted aryl, optionally substituted cycloalkyl, optionally substituted heterocyclyl, and optionally substituted heteroaryl;R2 is selected from H, halo, alkyl, alkenyl, alkynyl, -OH, alkoxy, alkenoxy, alkynoxy, -CN, -NO2, alkylthio, sulfoxido, sulfonyl, and amino;R5, R7 and R8 are each independently selected from H, halo, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, and amido;R6 is selected from H, halo, alkyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester,-CN, -NO2, amino, amido, sulfinamido, sulfonamido, optionally substituted heterocyclyl, optionally substituted heteroaryl, poly(ethylene glycol), and methoxypoly(ethylene glycol), orR6 and R7 together with atoms to which they are attached form an optionally substituted cycloalkyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl; andeach R9 is independently selected from halo, alkyl, -OH, alkoxy, -CN, and amino.

3. The method of claim 1 or claim 2, whereinn is 0, 1, 2, 3 or 4;R1 is selected from optionally substituted amino, optionally substituted aryl, optionally substituted cycloalkyl, optionally substituted heterocyclyl, and optionally substituted heteroaryl;R2 is selected from halo, alkyl, alkenyl, alkynyl, alkoxy, alkenoxy, alkynoxy, -CN, and -NO2;R5, R7 and R8 are each independently selected from H, halo, alkyl, alkenyl, hydroxy, and alkoxy;R6 is selected from halo, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -NO2, -CN, amino, and amido; andeach R9 is independently selected from halo, hydroxy, and alkoxy;optionally whereinn is 0 or 1;R1 is selected from optionally substituted amino, optionally substituted heterocyclyl, and optionally substituted heteroaryl;R2 is selected from alkyl, alkoxy, alkenoxy, alkynoxy, -CN, and -NO2;R5, R7 and R8 are each independently selected from H and alkoxy;R6 is selected from halo, alkyl, alkoxy, sulfoxido, sulfonyl, carboxy, ester, -NO2 and amido; and each R9 is independently halo or alkoxy.

4. The method of claim 2 or claim 3, wherein the angiogenesis is pathogenic angiogenesis;optionally wherein treating comprises increasing necrosis of pathogenic blood vessels; and / or2020365108   27 Aug 2026optionally wherein the subject has a disease or disorder selected from cancer, retinal occlusive vascular disease, retinopathy of prematurity, diabetic retinopathy, and age-related macular degeneration;optionally wherein the subject has cancer;optionally wherein the cancer is selected from the group consisting of colon cancer, breast cancer, prostate cancer, lung cancer, liver cancer, pancreatic cancer, ovarian cancer, bladder cancer, kidney cancer, esophageal cancer, cervical cancer, endometrial cancer, melanoma, brain cancer, glioma, neuroblastoma, osteosarcoma, chondrosarcoma, gastric carcinoma, mesothelioma, Kaposi sarcoma, liposarcoma, synovial sarcoma, or Wilm’s tumor; and / oroptionally wherein the subject has retinal occlusive vascular disease or retinopathy of prematurity; and / oroptionally wherein the subject has diabetic retinopathy; and / oroptionally wherein the subject has age-related macular degeneration.

5. A compound of Formula (I):r8                                (I),or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof;whereinn is 0, 1, 2, 3 or 4;R1 is an optionally substituted heterocyclyl;R2 is selected from H, halo, alkyl, alkenyl, alkynyl, -OH, alkoxy, C2-40alkenoxy, C2-40alkynoxy, -CN, -NO2, alkylthio, sulfoxido, sulfonyl, and amino;R5, R7 and R8 are each independently selected from H, halo, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, and amido;R6 is selected from H, halo, alkyl, hydroxy, alkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester, -CN, -NO2, amino, amido, sulfinamido, sulfonamido, heterocyclyl, heteroaryl, poly(ethylene glycol), and methoxypoly(ethylene glycol), orR6 and R7 together with atoms to which they are attached form a cycloalkyl, heterocyclyl, aryl, or heteroaryl; andeach R9 is independently selected from halo, alkyl, -OH, alkoxy, -CN, and amino; wherein the compound has at least one of the following:2020365108   27 Aug 20261) R2 is selected from C2-30alkyl, -OH, C1-40alkoxy, C2-40alkenoxy, C2-40alkynoxy, -NO2, alkylthio, sulfoxido, sulfonyl, and amino, wherea) when R2 is ethyl, then R6 is not methyl or methoxy, and / orb) when R2 is methoxy, then R6 is not halo, C1-2 alkyl or C1-2 alkoxy;2) R1 is an optionally substituted bridged heterocyclyl, optionally substituted fused heterocyclyl, or a substituted cycloheptyl;3) R1 is heterocyclyl substituted with one halo, amino, hydroxy, alkoxy, -CN, -NO2, alkyl, carboxy, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, optionally substituted cycloalkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, poly(ethylene glycol), or methoxypoly(ethylene glycol),where if the substituent is alkyl, the alkyl is further substituted with one substituent selected from halo, amino, alkoxy, -CN, -NO2, carboxy, ester, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, cycloalkyl, heterocyclyl, poly(ethylene glycol), methoxypoly(ethylene glycol), pyrrolidinyl and piperidinyl; or the alkyl is substituted with at least one -OR31, wherein R31 is poly(ethylene glycol) or methoxypoly(ethylene glycol); or4) R6 is alkyl substituted with at least one substituent selected from halo, amino, hydroxy, alkoxy, cycloalkoxy, heterocycloalkoxy, aryloxy, heteroaryloxy, poly(ethylene glycol)-oxy, methoxypoly(ethylene glycol)-oxy, -CN, -NO2, oxo, amido, carboxy, ester, alkylthio, sulfoxido, sulfonyl, sulfinamido, sulfonamido, heterocyclyl, cycloalkyl, aryl, heteroaryl, poly(ethylene glycol) and methoxypoly(ethylene glycol).

6. The compound of claim 5, wherein n is 0, 1 or 2; and / orwherein when R2 is C1-6 alkyl, R6 is not C1-6 alkyl or C1-6 alkoxy.

7. The compound of claim 5 or claim 6, wherein:a)      R1 is an optionally substituted heterocyclyl, such as an optionally substituted 5- to 9membered heterocyclyl, an optionally substituted 5- to 7-membered heterocyclyl, or an optionally substituted 5- to 6-membered heterocyclyl;b)      R1 is heterocyclyl substituted with at least one substituent selected from oxo, -OH, -OR28, -N(R28)2, alkyl, aryl, and heterocyclyl,the alkyl is substituted with at least one substituent selected from -N(R31)2, -S(O)0-2NR31R31, -C(O)N(R31)2, heterocyclyl, cycloalkyl, pyrrolidinyl and piperidinyl; orthe alkyl is substituted with at least one -OR31a, wherein R31a is poly(ethylene glycol) or methoxypoly(ethylene glycol); andeach R28 and R31 are independently H or alkyl;2020365108   27 Aug 2026c)      R1 is heterocyclyl substituted with a second heterocyclyl; andthe second heterocyclyl is unsubstituted or substituted with one or more substituents selected from -OH, -C(O)Oalkyl, -C(O)NHalkyl, alkyl, aryl, and heterocyclyl; andwherein the alkyl and heterocyclyl are each unsubstituted or substituted with one or moresubstituents selected from -OH, alkyl and aryl;d)      R1 isorwherein each s and t is independently 0, 1, 2 or 3, provided that the sum of s and t is 1, 2, 3, or 4;R20 is selected from alkyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl; andR20a is H, NH2, or OH;e)      R1 is heterocyclyl, optionally substituted with a sugar moiety;f)      R1 is selected from the group consisting of-321 -3 H- 322 -2020365108   27 Aug 2026g)      R1 is selected from the group consisting ofJXIXT\J     .JXrxJXr     WW     AM /     j\AA /            jWV         WW          AAA / och3 odd oocHs Loh Loh Loh YOh 0 00 o, and; orh)     R1 is selected from the group consisting ofWW  WW ww  ww     ww    ww   ww      ww   ww ww ww2020365108   27 Aug 2026and8.     The compound of any one of claims 5-7, wherein:a)      R2 is selected from C1-6 alkyl, -NO2, -OR18, and CN, and R18 is selected from C1-16 alkyl;b)     R2 is selected from -CH3, -CH2CH3, -CN, -NO2, and -OR18, and R18 is C1-16 alkyl; or2020365108   27 Aug 2026c)      R2 is -O(CH2)mCH3, wherein m is an integer selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11 12, 13, 14, and 15.

9. The compound of any one of claims 5-8, whereina)      R6 is selected from halo, alkyl, -OR17, -S(O)0-2R16, -C(O)OR15, -NO2, and -C(O)NR15R15;R15 is selected from H, methyl, ethyl, iPr, -CH2CH2NEt2, and -CH2CH2OH;R16 is methyl; andR17 is selected from methyl, trifluoromethyl and butyl;b)      R6 is halo, alkoxy, or alkyl;c)     R6 is -CH2CN, -OCF3, or NO2;d)     R6 is -SCH3, -SOCH3, or -SO2CH3;e)     R6 is -C(O)OCH3, or -C(O)OCH2CH3;f)      R6 is -C(O)NR15R15, one R15 is a sugar moiety, and the other R15 is H;g)     R6 is -C(O)NR15R15, and each R15 is independently selected from H, alkyl,heterocyclyl andh)     R6 is selected from the group consisting of10. The compound of any one of claims 5-9, wherein R5, R7, and R8 are each H; and / or wherein n is 1 or 2 and each R9 is independently halo.

11. The compound of any one of claims 5-10, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof wherein the compound is of Formula (II), Formula (III), or Formula (IV):2020365108   27 Aug 2026(II),(III), or(IV).

12. A compound of Formula (V):r8                          (V),or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof,whereineach of s, t, u, and v is independently 0, 1, 2, or 3, provided that the sum of s and t is 1, 2, 3 or 4, and the sum of u and v is 1, 2, 3 or 4;w is 0, 1, 2, or 3;Z1 is C or N,when Z1 is C, R20a is selected from H, halo, oxo, -NH2, -OH, -CN, -NO2, -OR28, -NHR28, -N(R28)2, -C(O)R28, -C(O)OR28, -C(O)OH, -OC(O)R28, -S(O)0-2R28, -NHS(O)0-2R28, -S(O)0-2NHR28, -NHS(O)0-2NHR28, -C(O)NH2, -C(O)NHR28, -C(O)N(R28)2, -NHC(O)R28, -OC(O)NHR28, - 326 -2020365108   27 Aug 2026-NHC(O)OR28, -OC(O)N(R28)2, -NR32C(O)NH2, -NR32C(O)NHR28, -NR32C(O)N(R28)2, poly(ethylene glycol), methoxypoly(ethylene glycol), C1-30 alkyl optionally substituted with OH or -C(O)OH, and C1-30 heteroalkyl optionally substituted with OH or -C(O)OH, wherein R32 is H or C1-4 alkyl, and R28 is C1-4 alkyl;when Z1 is N, R20a is absent;Z2 is C or N;Z3 is CH2, CHR25, CR25R25, NR25, O, or S(O)0-2 and R25 is selected from H and alkyl; andeach of n, R2, R5, R6, R7, R8, and R9 are as defined in claim 1.

13. A compound of Formula (XII):or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof;wherein:R1 is optionally substituted                  ;each of s, t, u, v, p and q is independently 0, 1, 2, or 3, provided that the sum of s and t is 1, 2, 3 or 4, the sum of u and v is 1, 2, 3 or 4, and the sum of p and q is 1, 2, 3 or 4;y is 0 or 1;z is 0 or 1;provided that y and z are not both 0;Z1 is C or N;when Z1 is C, R20a is H, halo, hydroxy, alkyl, or hydroxyalkyl;when Z1 is N, R20a is absent;Z2 is CH or N;Z3 is C or N;2020365108   27 Aug 2026when Z3 is C, R20b is H, halo, hydroxy, alkyl, or hydroxyalkyl;when Z3 is N, R20b is absent;Z4 is CH or N;Z5 is CH2, CHR25, CR25R25, C(=O), NR25, O, or S(O)0-2;each R25 is independently H, halo, alkyl or hydroxyalkyl;R211 is C2-40 alkyl, C2-40 alkenyl, or C2-40 alkynyl;R6 is H, halo, alkyl, haloalkyl, hydroxy, alkoxy, haloalkoxy, alkylthio, sulfoxido, sulfonyl, carboxy, ester,-CN, -NO2, amino, amido, sulfinamido, or sulfonamido; andR91 and R92 are independently selected from H and halo.

14. The compound of claim 13, wherein R211 is C5-30 alkyl;optionally wherein R211 is C10-25 alkyl; and / orwherein R91 and R92 are independently selected from H and F.

15. The compound of claim 13 or claim 14, wherein:a)      R6 is hydroxy, alkoxy,haloalkoxy, alkylthio, sulfoxido, or sulfonyl;b)      R6 is sulfoxido; orc)      R6 is methylsulfoxido.

16. The compound of any one of claims 13-15, wherein each heterocyclyl in R1 is independently and optionally further substituted with halo, hydroxy, alkyl, hydroxyalkyl, or oxo;optionally wherein R1 is selected from the group consisting ofch32020365108   27 Aug 2026optionally wherein R1 is selected from the group consisting of. and17. A compound selected from the group consisting of:366H3CNN         N No i 0 o 0 0vTVW2020365108   27 Aug 20263863873902020365108   27 Aug 20263943954612020365108   27 Aug 20264654662020365108   27 Aug 2026530542and2020365108   27 Aug 2026or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof.

18. A compound, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof, selected from the group consisting of:Structure Name 1 A 3-((4-ethylphenyl)sulfonyl)-4-(4- F3co 1 j lx methylpiperazin-1 -yl)-6-(trifluoromethoxy)quinoline F3C0^- 0 ? °\ / ° aVyi 3-((4-ethylphenyl)sulfonyl)-4-(piperidin- 1-yl)-6-(trifluoromethoxy)quinoline 0 4-(3-((4-ethylphenyl)sulfonyl)-6- F3CO |l \ . 1 / ? °\ / ° J J 1A (trifluoromethoxy)quinolm-4-yl)morpholine 3-((4-ethylphenyl)sulfonyl)-4-(4- ? °\ / ° methylpiperidin-1 -yl)-6- f3co s A^x (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name HO'Y 0 ? °\ / ° f3coxx^yysy^ Y Y Y Y 1 2-(4-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)piperazin-1 -yl)ethan-1 -ol 6 I1 ox / o f3c0^ Y Y Y Y Y 3-((4-ethylphenyl)sulfonyl)-4-(4-ethylpiperazin-1 -yl)-6-(trifluoromethoxy)quinoline 'i' ox o F3CO\^^Y^ , Y Y Y Y Y 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6- (trifluoromethoxy)quinoline OH 6 ? °\ / ° f5cova^YY Y Y Y Y Y 1-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolm-4-yl)piperidin-4-ol 0^0^ / 0 ? °\ z° Y Y J Y Y ethyl 4-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolm-4- yl)piperazine-1 -carboxylate (r’ 0 1 w 'Xijrci..... 3-((4-ethylphenyl)sulfonyl)-4-(4-(4-fluorophenyl)piperazin-1 -yl)-6-(trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name 0 °-" F3CO^    S TT J T JL 4-([1,4'-bipiperidin]-1'-yl)-3-((4- ethylphenyl)sulfonyl)-6- (trifluoromethoxy)quinoline 0 Ugh ? °\ / ° f3co^^.^3,s<^ TTJ TT 1-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-4-phenylpiperidin-4-ol Q 0 ? °\ / ° FaCO^^S^A^^st^Sj. T T T IjT 3-((4-ethylphenyl)sulfonyl)-4-(4-phenylpiperazin-1 -yl)-6-(trifluoromethoxy)quinoline s<. IT T IT 3-((4-ethylphenyl)sulfonyl)-4-(pyrrolidin- 1-yl)-6-(trifluoromethoxy)quinoline 6 ? °\ / ° F^CO^ / ^sx^TTT-^ TT J T1 1-(3-((4-ethylphenyl)sulfonyl)-6- methoxyquinolin-4-yl)piperidin-4-ol I LU n O M    ° 2v / \ / / °         / ° ethyl 4-(3-((4-ethylphenyl)sulfonyl)-6-methoxyquinolin-4-yl)piperazine-1 -carboxylate2020365108   27 Aug 2026Structure Name 0 3-((4-ethylphenyl)sulfonyl)-4-(4-(4- 0 fluorophenyl)piperazin-1 -yl)-6- h3co methoxyquinoline JI J L JL N-cyclohexyl-3-((4- H3CO [1 w — \ / ° un r ethylphenyl)sulfonyl)-6- methoxyquinolin-4-amine F. n 3-((4-ethylphenyl)sulfonyl)-N-(4- h3co II ?h °\ / ° Y Y Y 1 fluorophenyl)-6-methoxyquinolin-4-amine H3CO 0 ? °\ / ° ^Xj^xx^5^^^ 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4- (4-methylpiperazin-1 -yl)quinoline H3CO ¥ 3\ / ° Y Y Y I 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4-(piperidin-1 -yl)quinoline H3CO If C°^ ? °x / 0 Y Y Y 1 'x / ^N^ 4-(3-((4-ethylphenyl)sulfonyl)-6-methoxyquinolin-4-yl)morpholine H3CO Q ? °x / ° ^Y^JsY^ 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4- (4-methylpiperidin-1 -yl)quinoline 1 j 11 ,12020365108   27 Aug 2026Structure Name uF o — \ / ° — 3-((4-ethylphenyl)sulfonyl)-4-(4- ethylpiperazin-1 -yl)-6-methoxyquinoline ^x o c / 1 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4-(pyrrolidin-1 -yl)quinoline I o — \ / ° — — IS) 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4- (4-phenylpiperazin-1 -yl)quinoline 0 P,. T T J TO 4-([1,4'-bipiperidm]-1'-yl)-3-((4- ethylphenyl)sulfonyl)-6-methoxyquinoline i o CyCDp^O M / z° co p° 1-(3-((4-ethylphenyl)sulfonyl)-6-methoxyquinolin-4-yl)-4-phenylpiperidin-4-ol J CO oz \___, g x1 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline2020365108   27 Aug 2026Structure Name J o nT 3-((4-ethylphenyl)sulfonyl)-4-(4-isopropylpiperazin-1 -yl)-6-methoxyquinoline 9- Y Y Y Y I '''■-''^''N'^    \z"\ / 4-(azepan-1 -yl)-3-((4-ethylphenyl)sulfonyl)-6-methoxyquinoline / \ —2 —\ 3-((4-ethylphenyl)sulfonyl)-6-methyl-4-(4-methylpiperazin-1 -yl)quinoline / / Y / /  V— / x° _^° 3-((4-ethylphenyl)sulfonyl)-6-methyl-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline d 7 0. .0 Y Y Y Y "1 1-(3-((4-ethylphenyl)sulfonyl)-6-methylquinolin-4-yl)piperidin-4-ol 0 9° Y Y Y Y JL 4-([1,4'-bipiperidin]-1'-yl)-3-((4- ethylphenyl)sulfonyl)-6-methylquinoline2020365108   27 Aug 2026Structure Name 3-((4-ethylphenyl)sulfonyl)-6-methyl-4-(piperidin-1 -yl)quinoline 6 I1 0    0 Fx / ^XX^ IT J |O 3-((4-ethylphenyl)sulfonyl)-6-fluoro-4-(4-methylpiperazin-1 -yl)quinoline ox^~^ / ( / ) oz \___, / —\ /    z—<z   z V 'C ll. 3-((4-ethylphenyl)sulfonyl)-6-fluoro-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline 6 ? °\ / ° Fx^ / ^Jx^S^^^ IT J Y 1 1-(3-((4-ethylphenyl)sulfonyl)-6- fluoroqumolm-4-yl)piperidm-4-ol Tl €Y° / ^7° 4-([1,4'-bipiperidin]-1'-yl)-3-((4- ethylphenyl)sulfonyl)-6-fluoroquinoline °x^~^ Ys u_ 3-((4-ethylphenyl)sulfonyl)-6-fluoro-4-(piperidin-1 -yl)quinoline2020365108   27 Aug 2026Structure Name 0 HO F3CO 7 0 0 Y Y Y JL 2-(4-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-1,4-diazepan-1 -yl)acetic acid F3CO 0 / ^YYsY^ I I H 1 4-([1,4'-bipiperidin]-1'-yl)-3-((4- methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinoline J      H |<  ^^0^ F3CO L 5 ? °\z° -^YYsY^ Y Y Y X 1-(3-((4-methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol CN A F3CO 9 9 H 1 4-(4-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperazin-1 -yl)benzonitrile J H F3C0 Q i ? °\ / ° / ^AYsY^ 3-((4-ethylphenyl)sulfonyl)-4-(4-(pyrrolidin-1 -yl)piperidin-1 -yl)-6-(trifluoromethoxy)quinoline J [1 \x\ / 2020365108   27 Aug 2026Structure Name C)  \— /  \— / o ethyl 1 -(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4- yl)piperidine-4-carboxylate "6 ? °\ / ° FaCO. / ^.J^ I T J 11 X^  X / xX (1 -(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)piperidin-4-yl)methanol o ? °\ / ° FaXxxAPP / ^ T T J IA x'R X / V N-benzyl-3-((4-ethylphenyl)sulfonyl)-N-methyl-6-(trifluoromethoxy)qumolm-4-amine / ° / RP R« in 3-((4-ethylphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (trifluoromethoxy)qumolm-4-amme / / ^ < N I1 ox / o '“OpiX 3-((4-ethylphenyl)sulfonyl)-4-( 1H-1,2,4-triazol-1 -yl)-6- (trifluoromethoxy)quinoline °x / ° ? °\ / ° FaCO^^Pi^RC^^ 'X'-X 8-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)-1,4-dioxa-8-azaspiro[4.5]decane2020365108   27 Aug 2026Structure Name Y Y Y |O X / \Z 1-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)piperidine-4-carboxylic acid 0 Q., Y Y Y Y JX 4-((4-([1,4'-bipiperidm]-r-yl)-6- (trifluoromethoxy)quinolin-3 -yl)sulfonyl)benzonitrile 0 J^V nc^TXj VX 2-(4-([1,4'-bipiperidin]-1'-yl)-3-((4- ethylphenyl)sulfonyl)quinolin-6-yl)acetonitrile O \) ,.0 T\ rx^y^y o 4-([1,4'-bipiperidin]-1'-yl)-3-((3,4- dimethoxyphenyl)sulfonyl)-6- (trifluoromethoxy)quinoline XN^X^ °\ / ° Y Y Y Y Y 3-((3,4-dimethoxyphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6- (trifluoromethoxy)quinoline □J1^ C / \ O' o o \ / 1-(3-((3,4-dimethoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4- yl)piperidin-4-ol2020365108   27 Aug 2026Structure Name 0 CL U J II \- / ^N02 4-([1,4'-bipiperidin]-1'-yl)-3-((4- nitrophenyl)sulfonyl)-6- (trifluoromethoxy)quinoline XN^\^ ox / o CC0\ / xJxJ S Xis, Y Y Y Y JI ^''-'''^NO-, 4-(4-methyl- 1,4-diazepan-1 -yl)-3-((4-nitrophenyl)sulfonyl)-6-(trifluoromethoxy)quinoline OH 6 ? °\ / ° Il J II nO2 1-(3-((4-nitrophenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol o / ° o QX ( / / / ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4-hydroxypiperidin-1 -yl)quinoline-6-carboxylate Xn^j^ H ^1 0x / 0 / \ A / ^XX / ^ 0 VXJ V1 ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline-6-carboxylate > o Y° \—o '—' —' ethyl 4-([1,4'-bipiperidin]-1'-yl)-3-((4-ethylphenyl)sulfonyl)quinoline-6-carboxylate2020365108   27 Aug 2026Structure Name OH A 3-((4-ethylphenyl)sulfonyl)-4-(4- ?              0 hydroxypiperidin-1 -yl)quinoline-6- .0 '(Z> x o X carboxylic acid 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl- 9     7 a a 1,4-diazepan-1 -yl)quinoline-6-carboxylic AY acid 0 1 4-([1,4'-bipiperidin]-1'-yl)-3-((4- ethylphenyl)sulfonyl)qumolme-6- l^I°vA carboxylic acid YY ^i1 ^0  0 3-((3,4-dimethoxyphenyl)sulfonyl)-N,N- diethyl-6-(trifluoromethoxy)quinolin-4- Y Y Y IT amine X""       x0x HO. / \ |H°x / ° 2-((3-((3,4-dimethoxyphenyl)sulfonyl)-6- ^TYVAA (trifluoromethoxy)quinolin-4- kANJ VA0 / yl)amino)ethan-1 -ol 1-(3-((3,4-dimethoxyphenyl)sulfonyl)-6- ? °\ / ° (trifluoromethoxy)quinolin-4- F,COX / >. / A ^S<      ,.

0. ¥ T Y IT yl)piperidin-3-ol [ 3-((3,4-dimethoxyphenyl)sulfonyl)-N,N- o. .0 F3C0\ / 5x Yx / Sx / <X z°X dipropyl-6-(trifluoromethoxy)quinolin-4- Y Y Y Y Y amine2020365108   27 Aug 2026Structure Name o s .0 o O )= / x / o ■ ^ro 2,2'-((3-((3,4-dimethoxyphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4- yl)azanediyl)bis(ethan-1 -ol) uT"1 Y o o \ / N,N-dibutyl-3-((3,4- dimethoxyphenyl)sulfonyl)-6- (trifluoromethoxy)quinolin-4-amine 6 7 °\ / ° 02N X^vAx / S V^X 1 T J 11 X / X / 1-(3-((4-ethylphenyl)sulfonyl)-6-mtroquinolm-4-yl)piperidm-4-ol 7 °x / ° °2Nx / X / xJ T T J T 1 \ / \N^  x / \ / 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6-nitroquinoline 0 ¢0 °2N           S0z<X Y T T TO 4-([1,4'-bipiperidin]-1'-yl)-3-((4- ethylphenyl)sulfonyl)-6-nitroquinoline rO ^oC K ( o N,N-diethyl-3-((4-ethylphenyl)sulfonyl)- 6-nitroquinolin-4-amine2020365108   27 Aug 2026Structure Name ? °\ / ° s Cx'Xx, IJL J 11 3-((4-ethylphenyl)sulfonyl)-6-methoxy-4- (1H-1,2,4-triazol-1 -yl)quinoline N / 0        N n n .....’’a^o....... ethyl 3-((4-ethylphenyl)sulfonyl)-4-( 1H- 1,2,4-triazol-1 -yl)quinoline-6-carboxylate ? °\ / ° FaCO^x^xPp s( / x iX J 1A N,N-diethyl-3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-amme OH °\ / ° FaCO^ / x / kJ S Cx^x 1x1 J 1x1 1-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)piperidin-3-ol ^'N^'i L ^Nx lV / 0 HaCO^xx^^dpSp^xx IT J 1x1 ^xx^N^  x / v 3-((4-ethylphenyl)sulfonyl)-6-methoxy-N-(4-methylpiperazin-1 -yl)quinolin-4-amine oz \___, 1- / % dp / o=\ o (. ethyl 3-((4-ethylphenyl)sulfonyl)-4-((4-methylpiperazin-1 -yl)amino)quinoline-6-carboxylate \ o dpi dp / o 3-((4-methoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (trifluoromethoxy)quinolin-4-amine2020365108   27 Aug 2026Structure Name r-N / T w N. / 3-((4-methoxyphenyl)sulfonyl)-4-( 1H- ? °\ / ° 1,2,4-triazol-1 -yl)-6- (trifluoromethoxy)quinoline ? °\ / ° N,N-dibutyl-3-((4-ethylphenyl)sulfonyl)- I I 1 T 1 6-(trifluoromethoxy)quinolin-4-amine XN^ L N 3-((3,4-dimethoxyphenyl)sulfonyl)-N-(4- ^0 0 F,CO^          )st      .0, methylpiperazin-1 -yl)-6- T T T T T (trifluoromethoxy)quinolin-4-amine ^\\ Nx / 3-((3,4-dimethoxyphenyl)sulfonyl)-4- ? °\ / ° FqCO^           ^sC (1H-1,2,4-triazol-1 -yl)-6- 1                                                                                                                                   1 (trifluoromethoxy)quinoline N-(4-methylpiperazin-1 -yl)-6- L ?H0. / 0 (trifluoromethoxy)-3 -((4- FsCOx^^^L^ s 11 11    11 1 (trifluoromethoxy)phenyl)sulfonyl)quinol N^   \^^OCF3 in-4-amine nF^ 4-(1H-1,2,4-triazol-1 -yl)-6- ^00 (trifluoromethoxy)-3 -((4- FjCOx / ^^X^^t' / ^ T T T T X (trifluoromethoxy)phenyl)sulfonyl)quinol <^K'OCF3 ine 3-((4-butoxyphenyl)sulfonyl)-N-(4- F3C0'^^X^^s'X^ methylpiperazin-1 -yl)-6- UJ U / ^\ (trifluoromethoxy)quinolin-4-amine2020365108   27 Aug 2026Structure Name F\\ N > 3-((4-butoxyphenyl)sulfonyl)-4-( 1H- F3C0^^ 1,2,4-triazol-1 -yl)-6- I vU (trifluoromethoxy)quinoline N 3-((4-methoxyphenyl)sulfonyl)-N-(4- °2Nx / "iHoxzo A X methylpiperazin-1 -yl)-6-nitroquinolin-4- Y Y 1 / amine OH 2-((3-((4-ethylphenyl)sulfonyl)-6- f3cox^ v¥ x° «• (trifluoromethoxy)quinolin-4-yl)amino)ethan-1 -ol N, 2 3-((3,4-dimethoxyphenyl)sulfonyl)-6,7- 1 ? °\ / ° Y Y 1 / °\ dimethoxy-4-( 1H-1,2,4-triazol-1 -yl)quinoline °2N\ / Y A N > ? °\ / ° ^xOsA^ 1 T T 3-((4-methoxyphenyl)sulfonyl)-6-nitro-4-(1H-1,2,4-triazol-1 -yl)quinoline A NX y 2-(3-((4-methoxyphenyl)sulfonyl)-4-( 1H- ? °\ / ° 1,2,4-triazol-1 -yl)quinolin-6-yl)acetonitrile ^N' N 2-(3-((4-methoxyphenyl)sulfonyl)-4-((4- yH0 0 / AAsA^ methylpiperazin-1 -yl)amino)quinolin-6- Y Y ¥ yl)acetonitrile2020365108   27 Aug 2026Structure Name N^X N,N-diethyl-2-(4-(3-((4- ) N ~  ~ ethylphenyl)sulfonyl)-6- F3COx / 1 °X z° (trifluoromethoxy)quinolin-4-yl)-1,4- [f Y Y Y "1 ■ / V  \ / 'X diazepan-1 -yl)ethan-1 -amine •A) A N,N-diethyl-2-((1-(3-((4- ethylphenyl)sulfonyl)-6- (trifluoromethoxy)quinolin-4- F3CO^ / Y YYX A J 1A XxXX yl)piperidin-4-yl)oxy)ethan-1 -amine OH A 0 A 1'-(3-((4-ethylphenyl)sulfonyl)-6- (trifluoromethoxy)quinolin-4-yl)-[1,4‘- kA bipiperidin]-4-ol f3co^z II AY / x A    h A Ax Xxxx kJ A N,N-diethyl-1-(3-((4- ethylphenyl)sulfonyl)-6- F3CO^ / T A A ? °X z° AzsA Y Y Y Y (trifluoromethoxy)quinolin-4-yl)piperidin-4-amine XX A Axz HO—y ^0^ / 0 5-((3-((4-ethylphenyl)sulfonyl)-6- (trifluoromethoxy)quinolin-4- F3CO^, xYAsYxx Y J Y JL xXN /  X^XxX yl)amino)pentan-1 -ol N 3-((4-ethylphenyl)sulfonyl)-N-(piperidin- F3CO^ / AhA / O ^x A X / =x 1-yl)-6-(trifluoromethoxy)quinolin-4- Y Y Y X amine \XXX2020365108   27 Aug 2026Structure Name o 3-((4-ethylphenyl)sulfonyl)-N-(pyridin-4-ylmethyl)-6-(trifluoromethoxy)quinolin-4-amine A '™0 0 IT J I 1 A^ |A   '-^'''^ 3-((4-ethylphenyl)sulfonyl)-N-(pyridin-4-yl)-6-(trifluoromethoxy)qumolm-4-amme Q -.^A>A 1 T J T 1 Av AA / 3-((4-ethylphenyl)sulfonyl)-4-(1H-pyrrol- 1-yl)-6-(trifluoromethoxy)quinoline nD ? A / ° wa  xAsAx T T J ]O Av 3-((4-ethylphenyl)sulfonyl)-4-( 1H-pyrazol-1-yl)-6-(trifluoromethoxy)quinoline na N^Z I1 °\ / ° '"Ara.,. 3-((4-ethylphenyl)sulfonyl)-4-( 1H-1,2,3-triazol-1 -yl)-6- (trifluoromethoxy)quinoline HO |H°x / ° F3C0\^^AxAS^x<^ 1A J 1A N^  \A\ / 4-((3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolm-4-yl)amino)butan-1 -ol / / AN vC> ? °\ / ° U J 1A AA^ N^ AAA 4-(1H-benzo[d] [ 1,2,3]triazol-1 -yl)-3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name o XFXX^X y O\ 1'-(3-((4-methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)-[1,4‘-bipiperidin]-4-ol 0 3 O 02N       5 Y% ¥ Y Y Y X 4-([1,4'-bipiperidin]-1'-yl)-3-((4- methoxyphenyl)sulfonyl)-6-nitroquinoline \ o 45 c'Xp 2 2-(4-([ 1,4'-bipiperidin]-1'-yl)-3-((4- methoxyphenyl)sulfonyl)quinolin-6-yl)acetonitrile / \ o o .0 Y o 4-([1,4'-bipiperidin]-1'-yl)-6-butoxy-3-((3,4- dimethoxyphenyl)sulfonyl)quinoline Y ? °\ / ° 3-((4-ethylphenyl)sulfonyl)-4-(4-methyl-1H-imidazol-1 -yl)-6-(trifluoromethoxy)quinoline ,x a>u. 3-((4-ethylphenyl)sulfonyl)-4-( 1H-imidazol-1 -yl)-6- (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name J ocm g 4-([1,4'-bipiperidin]-1'-yl)-3-((4- butoxyphenyl)sulfonyl)-6- (trifluoromethoxy)quinoline m o = 0 o Q 4-([1,4'-bipiperidin]-1'-yl)-6-(trifluoromethoxy)-3 -((4-(trifluoromethoxy)phenyl)sulfonyl)quinol ine 0 7 0. 0 / s           s       ° \ Y Y Y Y Y 4-([1,4'-bipiperidin]-1'-yl)-3-((3,4- dimethoxyphenyl)sulfonyl)-6-(methylthio)quinoline 0 7 0. 0 / Ox / ^YY^Y^v^X Y Y Y Y Y 4-([1,4'-bipiperidin]-1'-yl)-3-((3,4-dimethoxyphenyl)sulfonyl)-6,7-dimethoxyquinoline / \ o o IZ1 __\ oz^ o 6-butoxy-3-((3,4- dimethoxyphenyl)sulfonyl)-N,N-diethylquinolin-4-amine 7 °\ / ° / s \^^YYs0 \ Y Y Y Y Y N,N-dibutyl-3-((3,4- dimethoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-amine2020365108   27 Aug 2026Structure Name N — N H " V „N ? °\ / ° 3-((4-ethylphenyl)sulfonyl)-4-( 1H-tetrazol-1-yl)-6-(trifluoromethoxy)quinoline q / ~^i I |V,O LLj Ll N-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)morpholin-4-amine 0 H0 r ? °\ / ° I T J T1 4-(4-ethylphenyl)-1 -(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)piperidin-4-ol 0 Ho / f °        1 Ox / O 0 cXj Y1 ethyl 4-(4-(4-ethylphenyl)-4-hydroxypiperidin-1 -yl)-3-((4- ethylphenyl)sulfonyl)quinoline-6-carboxylate 0 H°u ? °x / ° T T J T 1 4-(4-ethylphenyl)-1 -(3-((4-methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol2020365108   27 Aug 2026Structure Name OH '0 A LU A. ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4-hydroxy-[1,4'-bipiperidin]-1‘- yl)quinoline-6-carboxylate °        7     / 0 J-L / 1 ^sC uj IL ethyl 4-(4-(2-(diethylamino)ethyl)-1,4- diazepan-1 -yl)-3-((4- ethylphenyl)sulfonyl)qumolme-6-carboxylate 'xL 0    [^^0  0 ■■’ouo...... ethyl 4-(4-(2- (diethylamino)ethoxy)piperidin-1 -yl)-3-((4-ethylphenyl)sulfonyl)quinoline-6-carboxylate N^ / I Iv ^° LU T1 ethyl 4-(1H-benzo [d] [ 1,2,3]triazol-1 -yl)-3-((4-ethylphenyl)sulfonyl)quinoline-6-carboxylate H H        1 tU° A xx A A uu A ethyl 3-((4-ethylphenyl)sulfonyl)-4-( 1H-imidazol-1 -yl)quinoline-6-carboxylate H0^ / \ H         1 0x / 0 A A X / ¾. °CXT Ti ethyl 3-((4-ethylphenyl)sulfonyl)-4-(3-hydroxypiperidin-1 -yl)quinoline-6-carboxylate2020365108   27 Aug 2026Structure Name 0 0              0 ......-Wo. ethyl 4-([1,4'-bipiperidin]-1'-yl)-3-((4-methoxyphenyl)sulfonyl)qumolme-6-carboxylate H         1 °x / ° 0 iQj TX ethyl 4-(3-hydroxypiperidin-1 -yl)-3-((4-methoxyphenyl)sulfonyl)qumolme-6-carboxylate OH ¢) 0   ^Oxzo J-L uj U, N             0 ethyl 4-(4-hydroxy-[1,4'-bipiperidin]-1'- yl)-3-((4- methoxyphenyl)sulfonyl)quinoline-6-carboxylate 4b ° ? 0 0 0 uj T1 ethyl 4-(4-(2-(diethylamino)ethyl)-1,4-diazepan-1 -yl)-3-((4- methoxyphenyl)sulfonyl)quinoline-6-carboxylate 0 0   ^Ox / o / L uj n. ethyl 4-(4-(2- (diethylamino)ethoxy)piperidin-1 -yl)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate "3 0        N o o ........^eo. ethyl 4-(1H-imidazol-1 -yl)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate2020365108   27 Aug 2026Structure Name < yJ 0        N o n .........wo...... ethyl 4-(1H-benzo [d] [ 1,2,3]triazol-1 -yl)-3-((4-methoxyphenyl)sulfonyl)qumolme-6-carboxylate 0 0              n -Wo, 4-([1,4'-bipiperidin]-1'-yl)-3-((4-methoxyphenyl)sulfonyl) -N -methylquinoline-6-carboxamide \ o o OA (\jry ° \ o ( ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline-6-carboxylate X0 0 Hod ? °\ / ° F;COxAvzoJSt z<x I T J 11 ir   x / o / 1-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)-4-(4-methoxyphenyl)piperidin-4-ol / °\Ws u Hod ? °\ / ° F3c°, / xJ^^ IT J 1X 1-(3-((4-ethylphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)-4-(3-methoxyphenyl)piperidin-4-ol2020365108   27 Aug 2026Structure Name J ° o o 4-(benzo[d][1,3]dioxol-5-yl)-1-(3-((4- ethylphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol 'o 0 HO J 1 Iv ^°lu 11 ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4- hydroxy-4-(4-methoxyphenyl)piperidin- 1 -yl)quinoline-6-carboxylate hoT 0     nY n '"......ri".....:>..... ethyl 3-((4-ethylphenyl)sulfonyl)-4-(4- hydroxy-4-(3-methoxyphenyl)piperidin- 1 -yl)quinoline-6-carboxylate Yx / y H0J ? °\ / ° F3C0-.. U J 1A 4-(3-methoxyphenyl)-1-(3-((4-methoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)piperidin-4-ol 8 y} zCz v ) --\ o ^~~~~^ c" o 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6-(trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name 8 M C • o o 1'-(3-((4-butoxyphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)-[1,4‘-bipiperidin]-4-ol OH 0 'i, Y Y Y IT 1'-(3-((3,4-dimethoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-[1,4‘-bipiperidin]-4-ol o 7 0 0 / s -x^^vYsY5     ° \ Y Y Y Y Y 3-((3,4-dimethoxyphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6- (methylthio)quinoline H Jk / k J'st 0 ilIj T1 ethyl 4-(dibutylamino)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate HO       OH H         1 °x / 0 °^XY YY ethyl 4-(bis(2-hydroxyethyl)amino)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxylate ^o ,- ■Y o ( ethyl 4-([1,4'-bipiperidin]-1'-yl)-3-((4-butoxyphenyl)sulfonyl)quinoline-6-carboxylate2020365108   27 Aug 2026Structure Name H         °\ / ° Jk x^x A AC ixxxi^ ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline-6-carboxylate c ¢. ■ / 5 X / Uj: S LA J LA xx ^N          0 x 4-([1,4'-bipiperidin]-1'-yl)-3-((4- butoxyphenyl)sulfonyl)-6-(methylthio)quinoline \ _ N-^\ ox / o LA J LA 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6-(methylthio)quinoline OH 6 L\zo / x A / x A > t / x 0 AU O x. / N  \^VVX ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-hydroxy-[1,4'-bipiperidm]-r- yl)quinoline-6-carboxylate ^o .O / / / / °" A 1 / \ / \ / / O-(   2-(   2—C   2 A 1'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-[1,4'-bipiperidin]-4-ol \ + in —O A o 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name \ / z° A- / o O --\ zo (ZY 0' o 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6-(methylsulfonyl)quinoline \ o ,p / —c / \__, 0x2 / zs__ / y_ / o=\ z—< c N,N-diethyl-3-((4- methoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxamide \ U      |0v / 0 A / x1X XV V V V x X H UU VC X / n   XX X N-(2-(diethylamino)ethyl)-3-((4-methoxyphenyl)sulfonyl)-4-(4-methyl-1,4-diazepan-1 -yl)quinoline-6-carboxamide ^o (Z) -x o—+ \ 4-([1,4'-bipiperidin]-1'-yl)-3-((4- butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinoline \ + cz>—O o Z    / )--Z    )--Z    )—O \\   / /   \   /   \   / X V / o 1'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4'-bipiperidin]-4-ol x __ / 2d ---\ ,O --- --- V o 4-([1,4'-bipiperidin]-1'-yl)-3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfonyl)quinoline2020365108   27 Aug 2026Structure Name OH 0 j 0. / °      I 0..0 TX J XI 1'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfonyl)quinolin-4-yl)-[ 1,4'-bipiperidin]-4-ol 0 N H 0<\ / O 0 LXT YX ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)piperidin-1 -yl)quinoline-6-carboxylate ^o . J A o ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)piperidin-1 -yl)quinoline-6-carboxylate o ° O°x / 0 A / kAX / ^ 0 UJ H / ethyl 4-(4-(azepan-1 -yl)piperidin-1 -yl)-3-((4-methoxyphenyl)sulfonyl)qumolme-6-carboxylate °H 0              o ...... ethyl 4-(3-hydroxy-[1,4'-bipiperidin]-1'- yl)-3-((4- methoxyphenyl)sulfonyl)quinoline-6-carboxylate I ^v0 ^Axt tx ethyl 4-(4-(hydroxymethyl)-[ 1,4'- bipiperidin]- 1'-yl)-3-((4- methoxyphenyl)sulfonyl)quinoline-6-carboxylate2020365108   27 Aug 2026Structure Name 0 0   ^oxzo N          0     \ ethyl 4-(4-(azepan-1 -yl)piperidin-1 -yl)-3-((4-butoxyphenyl)sulfonyl)qumolme-6-carboxylate xx\x0H S          0 zo ^AxVxi ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(3-hydroxy-[1,4'-bipiperidm]-r- yl)quinoline-6-carboxylate - 0   ^oxzo Jk / k 2^sC IXT XI ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(hydroxymethyl)-[ 1,4'-bipiperidin] -1'-yl)quinoline-6-carboxylate -N^ JX. ......'Wr.„ ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(4-(2-(piperidin-1 -yl)ethyl)- 1,4-diazepan- 1 -yl)quinoline-6-carboxylate N^ 0 ^N o n ......’ceo...... ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(4-(2-(pyrrolidin-1 -yl)ethyl)-1,4-diazepan-1 -yl)quinoline-6-carboxylate N-^X H         °\ / ° ^Ayx xi xx ^N         0 ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(2-(piperidin-1 -yl)ethyl)- 1,4-diazepan-1 -yl)quinoline-6-carboxylate2020365108   27 Aug 2026Structure Name N-"\ H            0  0 ^oAccVxx ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(2-(pyrrolidin-1 -yl)ethyl)-1,4-diazepan-1 -yl)quinoline-6-carboxylate < N 0        N o n ■'V^ ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(1H-1,2,4-triazol-1 -yl)quinoline-6-carboxylate / —N 0       N o o ..... ethyl 3-((4-methoxyphenyl)sulfonyl)-4-(1H-1,2,3-triazol-1 -yl)quinoline-6-carboxylate N —N H " < N 0        N n n ........^t'iX ethyl 3-((4-methoxyphenyl)sulfonyl)-4- (1H-tetrazol-1 -yl)quinoline-6-carboxylate N—N "n °       N 0xz0 N              0 ethyl 3-((4-butoxyphenyl)sulfonyl)-4- (1H-tetrazol-1 -yl)quinoline-6-carboxylate ^o X' (Z) --¾ o 4-(3-((4-butoxyphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)thiomorpholine / / ^ < N H         1 0.,0 0 iCo Xl ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1H-1,2,4-triazol-1 -yl)quinoline-6-carboxylate2020365108   27 Aug 2026Structure Name H         1 °xZ° kk      J. N            0 ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1H-1,2,3-triazol-1 -yl)quinoline-6-carboxylate X < N 0        N 0 O ■Tayo,.......... ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1H-1,2,4-triazol-1 -yl)quinoline-6-carboxylate ^o ,O °A / \ zO z—e z o o=( o ( ethyl 3-((4-butoxyphenyl)sulfonyl)-4- thiomorpholinoquinoline-6-carboxylate \ N"\ 1    0             0 0 X Jk X X H 1 A J u X 3-((4-butoxyphenyl)sulfonyl)-N-isopropyl-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline-6-carboxamide h H0        H        7 ° / ° h°^<5h MO 3-((4-butoxyphenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-N-((4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)quinoline-6-carboxamide B H         1 0.,0 0 aXT XX ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1H-imidazol-1 -yl)quinoline-6-carboxylate i X JX X\ Xc 0 lxTX-^. ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1 -oxidothiomorpholino)quinoline-6-carboxylate2020365108   27 Aug 2026Structure Name o 2=0 o TATA-0 MXo ( / / 0' o ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(1,1 -dioxidothiomorpholmo)qumolme-6-carboxylate 0 0 7 °\ / ° IT T T T 4-(3-((4-butoxyphenyl)sulfonyl)-6-(trifluoromethoxy)qumolm-4-yl)thiomorpholine 1 -oxide Ox / ,° 0 7 °\ / ° F3C0..,^Xx / T^Sx 1 y j 1 a 4-(3-((4-butoxyphenyl)sulfonyl)-6-(trifluoromethoxy)quinolin-4-yl)thiomorpholine 1,1 -dioxide \ N^ H     TOx / O A^T / X j ext Ti N^  O / Oo / X / X 3-((4-butoxyphenyl)sulfonyl)-N,N-diethyl-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline-6-carboxamide o 2=o vxCj O o 3-((4-butoxyphenyl)sulfonyl)-N-(2-hydroxyethyl)-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline-6-carboxamide o '—z \=° o — \ / ° — — <x o 4-([1,4'-bipiperidin]-1'-yl)-3-((4- butoxyphenyl)sulfonyl) -N,N -diethylquinoline-6-carboxamide o 2=0 (A vjTCD^O A O' o 4-([1,4'-bipiperidin]-1'-yl)-3-((4-butoxyphenyl)sulfonyl)-N-(2-hydroxyethyl)quinoline-6-carboxamide2020365108   27 Aug 2026Structure Name J / =o — \ / ° — — o' o 4-([1,4'-bipiperidin]-1'-yl)-3-((4- butoxyphenyl)sulfonyl)-N- ethylquinoline-6-carboxamide A OH     9       ? °\ / ° o. <    k    A Y HoAyr-AAAv >AA HO^A\ H II A       II A, 4-(1H-imidazol-1-yl)-3-((4- methoxyphenyl)sulfonyl) -N-((4R,5S,6R)-2,4,5-trihydroxy-6- (hydroxymethyl)tetrahydro-2H-pyran-3-yl)quinoline-6-carboxamide < yJ OH      H         ? 0  0 o^ A / \ A A / \ hoYA-^n^A^Y hAa h II A J II J OH 4-(1H-benzo[d] [ 1,2,3]triazol-1 -yl)-3-((4-methoxyphenyl)sulfonyl) -N-((4R,5S,6R)-2,4,5-trihydroxy-6- (hydroxymethyl)tetrahydro-2H-pyran-3-yl)quinoline-6-carboxamide o A' uy O' 3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)-4-(4-(2-(piperidin-1 -yl)ethyl)- 1,4-diazepan-1 -yl)quinoline \ fA >A O' 3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)-4-(4-(2-(pyrrolidin-1 -yl)ethyl)- 1,4-diazepan-1 -yl)quinoline \ + (zi — O (z> /                    O O"    ' o 1'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4'-bipiperidin]-3-ol2020365108   27 Aug 2026Structure Name •Vo O O' 3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(piperidin-1 -yl)ethyl)- 1,4-diazepan-1 -yl)quinoline N-^ °’         ox / o A A > t +Tj j Yj 3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(pyrrolidin-1 -yl)ethyl)- 1,4-diazepan-1 -yl)quinoline > o o o ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-methyl- 1,4-diazepan-1 -yl)piperidin-1 -yl)quinoline-6-carboxylate > UI o' o ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-morpholinopiperidin-1 -yl)quinoline-6-carboxylate ) o / =o y)    _ — \ / ° — — o' o ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-fluorophenyl)piperazin-1 -yl)quinoline-6-carboxylate o o ( ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-(2-hydroxyethyl)piperazin-1 - yl)piperidin-1 -yl)quinoline-6-carboxylate2020365108   27 Aug 2026Structure Name 0 °   ^Oxzo X \ / N         0 ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-phenyl-[1,4'-bipiperidin]-1'-yl)quinoline-6-carboxylate > J’ x^cycyo - o ethyl 4-([ 1,4':1',4"-terpiperidin]-1"-yl)-3-((4-butoxyphenyl)sulfonyl)qumolme-6-carboxylate ^o . / 5 o < ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-thiomorpholinopiperidin-1 -yl)quinoline-6-carboxylate \ N^\ o. a xs y^zU 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6-(methylthio)quinoline J \ 4-([1,4'-bipiperidin]-r-yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline o X' .cm o—+ \ 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-methyl- 1,4-diazepan-1 -yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name o .: OCy o—+ \ 4-([1,4'-bipiperidin]-1'-yl)-3-((4- (heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 6 ? °\ / ° XXXXX / ^ 1'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-[1,4‘-bipiperidin]-3-ol OH . .!.. / S\x^XpXSX^P> XX X XX 1'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-[1,4‘-bipiperidin]-4-ol \ + ^-O , —\ / ° — — V o 1'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4‘-bipiperidin]-4-ol \ o P’ oz \___, dp / °^\ o < ethyl 3-((4-methoxyphenyl)sulfonyl)-4-((4-methylpiperazin-1 - yl)amino)quinoline-6-carboxylate X" / Q o 2 / )--H X X 1 V3 p’ o 3-((4-methoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6-(methylthio)quinolin-4-amine2020365108   27 Aug 2026Structure Name .P I 2\ 2 dp / 1 o — 3-((4-methoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (methylsulfmyl)qumolm-4-amme 0_NX <0 0 d 0x / s             s Y Y Y Y J 3-((4-methoxyphenyl)sulfonyl)-N-(4-methylpiperazin-1 -yl)-6- (methylsulfonyl)quinolin-4-amine \ cf -; - d' o 4-(1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolm-4-yl)piperidm-4-yl)morpholine H0^^ 0 J ? °\ / ° TX J Tl / ^ 2-(4-(1-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolm-4-yl)piperidm-4-yl)piperazin-1 -yl)ethan-1 -ol Y 0. W >O 0' o 4-([1,4':1',4"-terpiperidin]-1"-yl)-3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinoline \ '0 H; ZM zvJ zYdj '—^o '—'   '—1 o '—' KT> u o 1'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-4-phenyl-[1,4'-bipiperidin]-4-ol2020365108   27 Aug 2026Structure Name 'r C 6 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-(4-fluorophenyl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylthio)quinoline zjxy OC "O \ 0 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4- 6 methyl- 1,4-diazepan-1 -yl)piperidin-1 -yl)- oo ? °\ z° H T 1 H 1 6-(methylthio)quinoline L C N c 4-(1 -(3-((4-butoxyphenyl)sulfonyl)-6- 6 (methylsulfmyl)qumolm-4-yl)piperidm-4- 0 1 A o yl)morpholine HO^^ Q 2-(4-(1-(3-((4-butoxyphenyl)sulfonyl)-6- A (methylsulfmyl)qumolm-4-yl)piperidm-4- 0 1 s + CC 7 0. .0 ^OASA^ Ti jT jT h j yl)piperazin-1 -yl)ethan-1 -ol LA L L,C 0 A 1 T T T 1 4-([1,4':r,4"-terpiperidm]-1"-yl)-3-((4- butoxyphenyl)sulfonyl)-6- 0 ' + (methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name ~L°h ?        7 °\ / ° *11J II 1'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfinyl)qumolm-4-yl)-4-phenyl-[1,4'-bipiperidin]-4-ol \ + tn —O ^■o-oo- 0’ o 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-(4-fluorophenyl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylsulfmyl)qumolme \ + tn—O o (1'-(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)-[1,4‘-bipiperidin]-4-yl)methanol ^o O-tn + \ 3-((4-butoxyphenyl)sulfonyl)-4-(4-(4-methyl- 1,4-diazepan-1 -yl)piperidin-1 -yl)-6-(methylsulfmyl)qumolme W O:' o o N,N-diethyl-2-(4-((4-(4-methyl-1,4- diazepan-1 -yl)-6-(methylthio)quinolin-3- yl)sulfonyl)phenoxy)ethan-1 -amine2020365108   27 Aug 2026Structure Name c TXJ 4-(1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)qumolm-4-yl)piperidm-4-yl)thiomorpholine o’ 6 9         o o XX X. Xt °CrxO ethyl 3-((4-butoxyphenyl)sulfonyl)-4-(4-(1 -oxidothiomorpholino)piperidin-1 -yl)quinoline-6-carboxylate \ + tn —O <1 . d' o 4-(1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)piperidm-4-yl)thiomorpholine Y ■d.._. cnz ' o 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)piperidin-1 -yl)-6-(methylthio)quinoline Y XoQ in o 0° ■ o 1'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)qumolm-4-yl)-[1,4‘-bipiperidin]-3-ol CZn^ N—\ ^X °\ / ° / 5        s X"^ 0 J XX 3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)-4-(4-(2-(piperidin-1 -yl)ethyl)- 1,4-diazepan-1 -yl)quinoline2020365108   27 Aug 2026Structure Name \ 0 6 ? 0K z0 XX J Li 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-methyl- 1,4-diazepan-1 -yl)piperidin-1 -yl)-6-(methylthio)quinoline 8 - o, o 0'°      ‘ o 2-(4-(1-(3-((4- (heptyloxy)phenyl)sulfonyl)-6-(methylthio)qumolm-4-yl)piperidm-4-yl)piperazin-1 -yl)ethan-1 -ol ¢000 " 0 4-([1,4':1',4"-terpiperidin]-1"-yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline 6 ? °x z° / / z / Z.Zz XX X XX , / / z^ 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-methylpiperazin-1 -yl)-6-(methylthio)quinoline \ y-O 1 Ozz ._• ' 0 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline \ y-O , X>Q ( / /                 O 0 1'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)-[1,4'-bipiperidin]-3-ol2020365108   27 Aug 2026Structure Name x—\ N—x °’ <\ / ° xx> 3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(piperidin-1 -yl)ethyl)- 1,4-diazepan-1 -yl)quinoline o .0 ■ ’ 0 ° \ 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-methyl- 1,4-diazepan-1 -yl)piperidin-1 -yl)-6-(methylsulfmyl)qumolme o , .o                             <s> O — m + \ 2-(4-(1-(3-((4- (heptyloxy)phenyl)sulfonyl)-6- (methylsulfmyl)qumolm-4-yl)piperidm-4-yl)piperazin-1 -yl)ethan-1 -ol \ + iz-O । C:- ■- ■-" o 4-([1,4':1',4"-terpiperidin]-1"-yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline \ + iz>-O । ■ : ’ -■ o 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-methylpiperazin-1 -yl)-6- (methylsulfinyl)quinoline I A OH   ?     lXz° °^     JI zz A Vz z- ho-^S-nY^^ V0 hcr^V h [1     1      1      [1     1 OH 3-((4-methoxyphenyl)sulfonyl)-4-((4-methylpiperazin-1 -yl)amino)-N-((4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)quinoline-6-carboxamide2020365108   27 Aug 2026Structure Name o 1'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-4-phenyl-[1,4'-bipiperidin]-4-ol \ + GO —Q - o 1'-(3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)qumolm-4-yl)-4-phenyl-[1,4'-bipiperidin]-4-ol \ -: .. - o 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline +v ■ ■ ‘ ■ o 1'-(3-((4-(decyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4‘-bipiperidin]-3-ol \      XX + tn-O -■ o 3-((4-(decyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(piperidin-1 -yl)ethyl)- 1,4-diazepan-1 -yl)quinoline \ XX Q- o 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(4-methyl- 1,4-diazepan-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline HO^ 0 ?- 0c\zo *XX X XX 2-(4-(1-(3-((4- (decyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)qumolm-4-yl)piperidm-4-yl)piperazin-1 -yl)ethan-1 -ol2020365108   27 Aug 2026Structure Name :. ■ - o 4-([1,4':1',4"-terpiperidin]-1"-yl)-3-((4-(decyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline °" XX^   XX-q-X / X^X^ 1'-(3-((4-(decyloxy)phenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)-4-phenyl-[1,4'-bipiperidin]-4-ol J - -: <z>                             O 0     g o 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-(2-mPEGoxyethyl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylthio)quinoline ■ ’ - o 3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)-4-(4-(2-(pyrrolidin-1 -yl)ethyl)piperazin-1 -yl)quinoline ■' 0 ? °\ / ° / 5 \xx>Yx / s xx lX X Ta N     X ^XX X / V 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(1 -methylpiperidin-4-yl)piperazin-1 -yl)-6-(methylthio)quinoline o X xYH - 4-(4-(1-benzylpyrrolidin-3-yl)piperazin-1-yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline2020365108   27 Aug 2026Structure Name 0 ? °\ / ° XX J XX 4-(4-((1 -benzylpiperidin-4-yl)methyl)piperazin-1 -yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline \ + tn-Q •: :. (Z< -■ o 3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(2-(pyrrolidin-1 -yl)ethyl)piperazin-1 -yl)quinoline o X - o-^ + \ 4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline o .b X 4-(4-(1-benzylpyrrolidin-3-yl)piperazin-1-yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline X o 4-(4-((1 -benzylpiperidin-4-yl)methyl)piperazin-1 -yl)-3-((4-(heptyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline -JL •_■ (z / o 0     * o 3-((4-(heptyloxy)phenyl)sulfonyl)-4-(4-(4-(2-mPEGoxyethyl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 0 3-((4-(heptyloxy)phenyl)sulfonyl)-6- < - ■ o (methylthio)-4-(4-(2-(piperidin-1 -yl)ethyl)piperazin-1 -yl)quinoline 0 3-((4-(heptyloxy)phenyl)sulfonyl)-6- C • -o (methylsulfinyl)-4-(4-(2-(piperidin-1 -yl)ethyl)piperazin-1 -yl)quinoline 6 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(1- o -.0 Q>-^ + \ ethylpiperidin-4-yl)piperazin-1 -yl)-6-(methylsulfinyl)quinoline H0'x^| ,N 2-(4-(1-(3-((4-((3,7- o .0 ' -0 O—co + \ dimethyloctyl)oxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1 -ol +v ¢.000 0° o 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline 0 A 4-(1'-(3-((4-(decyloxy)phenyl)sulfonyl)- M 6-(methylsulfinyl)quinolin-4-yl)-[1,4'- \ + CA-O A 0° o bipiperidin]-4-yl)morpholine2020365108   27 Aug 2026Structure Name \ 0 0 ?■  ¢00 ’Ll J Ll xx      xx ^q'- xx \x xx xx x 3-((4-(decyloxy)phenyl)sulfonyl)-4-(4-(4-methyl- 1,4-diazepan-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline 0 0.0 . ■ ■ ; _■ 0 \ 1''-(3-((4-(decyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4':r,4"-terpiperidin]-3-ol 0 .. -• -’ X M\ 4-([1,4':1',4''-terpiperidin]-1''-yl)-3-((4- ((3,7- dimethyloctyl)oxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline U-     O ■ ■ ° \ 4-([1,4':1',4"-terpiperidin]-1"-yl)-3-((4-(decyloxy)-3-fluorophenyl)sulfonyl)-6-(methylsulfinyl)quinoline H0'X~^ 0 ?- 0c\zo X s xx^xxLL s X / XyZ F ’Ll J LX XX ''N''   XX ''o "X XX XX xx x 2-(4-(1-(3-((4-(decyloxy)-3- fluorophenyl)sulfonyl)-6- (methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1 -ol +v <|xxo^ L 0 2-(4-(1'-(3-((4- (decyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4'-bipiperidin]-4-yl)piperazin-1 -yl)ethan-1 -ol2020365108   27 Aug 2026Structure Name / \ o o O=L0-O o \ N,N-diethyl-6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)qumolm-4-amine / \ o o X V o—Ln—o o \ N-ethyl-N-isopropyl-6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)qumolm-4-amine / \ o o IP v_\ s O-tn-O \ O N,N-dibutyl-6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)qumolm-4-amine / \ o o o O=Ln = O 0 O\ N1 -(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)-N 1,N2,N2-triethylethane- 1,2-diamine ^NH 0 1 H .

0. A. .s. TYj N1 -(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)- N2,N2-diethylethane- 1,2-diamine -A^N^P ^NH 0 1 II A. _s. YXj°V1 N1 -(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)- N3,N3-diethylpropane-1,3-diamine ^NH 0 1 H A. _s. YYy°Y^ N1 -(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinolin-4-yl)-N4,N4-diethylbutane- 1,4-diamine2020365108   27 Aug 2026Structure Name / \ \ 0 0 \ / 0=00=0 p 0 \ N3-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)- N1,N1 -diethylbutane- 1,3-diamine HO 0 N 0 1 H A. ,S. YYY syp 2-(4-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)piperazin-1 -yl)ethan-1 -ol 0 N 0 1 H / k\ / k / S. ^XXJ°O / 0        N             0 3-(4-(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinolin-4-yl)piperazin-1 -yl)-N,N-diethylpropan-1 -amine ¢ / V o=<^=o O\ 1 -(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)piperidin-4-ol / \ 0   0 )=<     0 Cj 0=^ = 0 P 0 \ (1-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)piperidin-3-yl)methanol HO Vo 1 H YYY °T1 1 -(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)pyrrolidin-3-ol / \ O   O / \ O=cn=O P O\ 6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)-4-((1S,4S)-5-methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)quinoline2020365108   27 Aug 2026Structure Name \ n- 0 O 4-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4-yl)- J 0 II xK / °x N,N-dimethyl- 1,4-diazepane-1 -carboxamide N '^\ / 0H 1 -(6,7-dimethoxy-3-((4- o o \ / "N^ x>. N 0 ii ZSX / SX methoxyphenyl)sulfonyl)qumolm-4-yl)- 4-phenylpiperidin-4-ol 0-^0 0 methyl 4-(1 -(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4- ^0. / J W 0 II 0^ yl)piperidin-4-yl)benzoate H O^^N 0 4-(1-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4- I >R 0 II yl)piperidin-4-yl)-N-methylbenzamide "'0 0 6,7-dimethoxy-4-(4-(4- methoxyphenyl)piperidin-1 -yl)-3-((4- / 0,x^ 1 ~'[\T / . 'N 0 II xS. x^ °x methoxyphenyl)sulfonyl)quinoline2020365108   27 Aug 2026Structure Name / \ o o 0 Q=G0=O 0 O\ 6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)-4-(4-(4-(pyrrolidin-1 -ylmethyl)phenyl)piperidin-1 -yl)quinoline o XNX 0 1 H YXy°i0 6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)-4-(3-phenylpyrrolidin-1 -yl)quinoline 0__ °00 NZ 0 1 H XXT°T0 4-(3-(benzo[d][1,3]dioxol-5- yl)pyrrolidin-1 -yl)-6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinoline / \ o o v0O~O O = co=O o o \ 6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)-4-(4-phenylpiperazin-1 -yl)quinoline \ o O = ^ = O x Z0A O—0 y—z z—\ z °\ / ° 6,7-dimethoxy-4-(4-(4-methoxyphenyl)piperazin-1 -yl)-3-((4-methoxyphenyl)sulfonyl)quinoline2020365108   27 Aug 2026Structure Name \ o O O = ^> = O Try- o o \ / ethyl 4-(4-(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)qumolm-4- yl)piperazin-1 -yl)benzoate 0 1 H Tn aYT 4-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)qumolm-4-yl)-1-(4-methoxyphenyl)piperazin-2-one H ^ny° u ¢^ 0. 1 II .X       / x TYj oYT N-cyclohexyl-4-(4-(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)qumolm-4-yl)piperazin-1 -yl)benzamide 0 0. 1 II XXXQ ^0       N           0 4-([1,4'-bipiperidin]-1'-yl)-6,7- dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinoline \ o O Q°| o o \ / 1-(1 -(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)quinolin-4- yl)piperidin-4-yl)pyrrolidin-2-one2020365108   27 Aug 2026Structure Name HO / \ c. 1 II / k / 5. / x ^XXj°TX / 0        N             0 (1-(1 -(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)qumolm-4-yl)piperidm-4-yl)pyrrolidm-2-yl)methanol H°^^\ N""\^ —N 0 1 H / --. A. ^s. xx / 0        N 2-(4-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)qumolm-4-yl)- 1,4-diazepan-1 -yl)ethan-1 -ol X \ c: 1 II / >. xk k-. xx ^XXkQ^ 0N 7-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)qumolm-4-yl)-1 -isobutyldecahydropyrido [4,3-e][1,4]oxazepine 'o o 0=1^ = 0 k^k vJ \ / 1 -((4-(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinolin-4-yl)-1,4-diazepan-1 -yl)methyl)cyclopentan-1 -ol ^—N  0 1 H XXjkCl 6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)-4-(4-(oxetan-3-yl)- 1,4-diazepan-1 -yl)quinoline Cl wk N^X N 0 1 H ^0.     J. / S. / <. TXT°Yk 6-chloro-2-(4-(6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)quinolin-4-yl)-1,4-diazepan-1 -yl)benzo[d]thiazole2020365108   27 Aug 2026Structure Name 0 U N 0 1 11 YYj 1 -(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)qumolm-4-yl)-4-methyl- 1,4-diazepan-5-one N'^X^ —N 0 1 H ,o.       A. XXj°TX 6,7-dimethoxy-3-((4-methoxyphenyl)sulfonyl)-4-(4-(tetrahydro-2H-thiopyran-4-yl)-1,4-diazepan-1 -yl)quinoline 0 II o=d-^ N''X^ N 0 1 II a        A. _s. TXj°Yi 4-(4-(6,7-dimethoxy-3-((4- methoxyphenyl)sulfonyl)qumolm-4-yl)-1,4-diazepan-1 -yl)tetrahydro-2H-thiopyran 1,1-dioxide 0 0            0 II                               1 II \ Jk     / k / S^ 1 IJ 0 LA / 4-([1,4'-bipiperidin]-1'-yl)-3-((4-methoxyphenyl)sulfonyl) -N,N -dimethylquinoline-6-carboxamide 0    ^N 0 X N    XX Q / 3-((4-methoxyphenyl)sulfonyl)-N,N-dimethyl-4-(4-(2-oxopyrrolidin-1 -yl)piperidin-1 -yl)quinoline-6-carboxamid / ^N N^X, 0 o 0    —N  0 II                            1             H \        X-U N    II ^1 XT H Ti X 1  I A J ° I A XX^n-^  XX^q / 4-(4-(2-(dimethylamino)-2-oxoethyl)-1,4-diazepan-1 -yl)-3-((4- methoxyphenyl)sulfonyl) -N,N -dimethylquinoline-6-carboxamide2020365108   27 Aug 2026Structure Name 0 o            o -=1:6=0.. 4-([1,4'-bipiperidm]-r-yl)-3-((4-methoxyphenyl)sulfonyl) -N -methylquinoline-6-carboxamide 0        N   0 II                                  1                II \ Jk / k N X  ^<IIT Y H i    J ° i 3-((4-methoxyphenyl)sulfonyl)-N-methyl-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline-6-carboxamide h° 7" \ N 0 k7 0 ■-OO-C, 4-(4-(2-(hydroxymethyl)pyrrolidin-1 -yl)piperidin-1 -yl)-3-((4-methoxyphenyl)sulfonyl) -N -methylquinoline-6-carboxamide ^k\r^ 0            0 \       k. .k. H (A J 0 (J. 4-([1,4'-bipiperidm]-1'-yl)-N-(2- (diethylamino)ethyl)-3-((4- methoxyphenyl)sulfonyl)quinoline-6-carboxamide 0     ^hT 0 1                                II                                 1 H \ / N.    X    A. ,s. N Y         T k H         J 0 N-(2-(diethylamino)ethyl)-4-(1 -isobutyloctahydropyrido[4,3-e] [ 1,4]oxazepin-7(5H)-yl)-3-((4-methoxyphenyl)sulfonyl)quinoline-6-carboxamide k.. ‘ 0 2-(4-(1-(3-((4- (dodecyloxy)phenyl)sulfonyl)-6- (methylsulfmyl)qumolm-4-yl)piperidm-4-yl)piperazin-1 -yl)ethan-1 -ol2020365108   27 Aug 2026Structure Name +v A. -. -. .-, r ■ o 2-(4-(1'-(3-((4- (dodecyloxy)phenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)-[1,4‘-bipiperidin]-4-yl)piperazin-1 -yl)ethan-1 -ol \ + cn —O c / t • o 3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline \ cn — Q rc -..., o 4-([1,4':r,4"-terpiperidm]-r'-yl)-3-((4-(dodecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline o . . - o -.- O~to \ 1"-(3-((4-(dodecyloxy)phenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)-[1,4':1',4"-terpiperidin]-3-ol H0'X^| 0 N 0oxzo s         A. 2-(4-(1-(6-(methylsulfinyl)-3-((4-(tetradecyloxy)phenyl)sulfonyl)qumolm-4-yl)piperidin-4-yl)piperazin-1 -yl)ethan-1-ol2020365108   27 Aug 2026Structure Name 0 0 °' _S. / ^ / 1 0-^ N       ^0                \^\ 2-(4-(1'-(6-(methylsulfinyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinolin- 4-yl)-[1,4'-bipiperidin]-4-yl)piperazin-1 - yl)ethan-1-ol 6 0 ?   ^Oz.O s. / -. J. J^sf / -. o x io 4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinoline 0 0 ° Oa 0 XX 7 TO 4-([1,4':1',4"-terpiperidin]-1"-yl)-6- (methyl(^1-oxidanyl)-^3-sulfanyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinoline / / .OH 0 ? Ot. 0 XX X XX 1"-(6-(methyl(^1-oxidanyl)- ^3-sulfanyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinolin-4-yl)-[1,4':1',4"-terpiperidin]-3-ol °^X 0. 1 II / S. / -. / X ,s. TXT°T1 1-(1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)piperidin-4-yl)pyrrolidin-2-one H0 / \ NX 0, 1 II / 5. / -. / k / S. / -. XXoTX / \ (1-(1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)piperidin-4-yl)pyrrolidin-2-yl)methanol2020365108   27 Aug 2026Structure Name 2-(4-(3-((4-butoxyphenyl)sulfonyl)-6- —N 0 (methylthio)quinolin-4-yl)-1,4-diazepan- / S.       / L ^s. / x fjT oYX 1-yl)ethan-1-ol ---- / —-NZ   \> 7-(3-((4-butoxyphenyl)sulfonyl)-6- 1 (methylthio)quinolin-4-yl)-1 - kn^ 0 X. isobutyldecahydropyrido [4,3- XXX °XX e][1,4]oxazepine f3c ) HN 4-(3-((4-butoxyphenyl)sulfonyl)-6- 0^ ' fX (methylthio)quinolin-4-yl)-N-(2,2,2- 0 trifluoroethyl)- 1,4-diazepane-1 - 1 H / S. / -. A. ,SX / -71      ^T II 7< Y sulfonamide IJX °1 N            0 OH xx^ n^'j 1-((4-(3-((4-butoxyphenyl)sulfonyl)-6- y—N 0 (methylthio)quinolin-4-yl)-1,4-diazepan- / S. / x. / X Y- / - / XXXoXX 1 -yl)methyl)cyclopentan-1 -ol X X\ X X X\ / \ Y       ^0 °x N— 3-((4-butoxyphenyl)sulfonyl)-6- ^X n o (methylthio)-4-(4-(oxetan-3-yl)-1,4- 1 II / S. / -. / k / S. / x Ti                 11 li X diazepan-1 -yl)quinoline [l k J M k „ —- 'N^   \^— Cl N^\ 2-(4-(3-((4-butoxyphenyl)sulfonyl)-6- N-^\ (methylthio)quinolin-4-yl)-1,4-diazepan- N   0 1          H 1 -yl)-6-chlorobenzo[d]thiazole / 5 / / x / X / S. / - / TXJ°XX / / / / 0 \A 1-(3-((4-butoxyphenyl)sulfonyl)-6- < > '—N   0 (methylthio)quinolin-4-yl)-4-methyl-1,4- ^S. —. / L ^5. —. xxx°xx diazepan-5-one —x—N^2020365108   27 Aug 2026Structure Name 0 1 H YX7SX1 3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)-4-(4-(tetrahydro-2H-thiopyran-4-yl)- 1,4-diazepan-1 -yl)quinoline 0 II —N 0 1 H / / J /       / / vxj^JlI N        o -^\ / \ 4-(4-(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)quinolin-4-yl)-1,4-diazepan- 1 -yl)tetrahydro-2H-thiopyran 1,1 -dioxide 0     ^NH 0 II                         1 H \     / / / U. ^s. / . N    Ti ^1       " h X H L kL J 0I JI ^ / ^ N^  \ / - o^ 3-((4-methoxyphenyl)sulfonyl)-N-methyl-4-(methylammo)qumolme-6-carboxamide ^o C O=un=O co \ 1-(1 -(3-((4-butoxyphenyl)sulfonyl)-6-(methylthio)qumolm-4-yl)piperidm-4-yl)pyrrolidin-2-one \ + co—o ■Gv------;■ O     -n 2-(4-(1-(3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl)-6- (methylsulfmyl)qumolm-4-yl)piperidm-4-yl)piperazin-1 -yl)ethanol \ + co —O O    -n 4-([1,4':1',4"-terpiperidin]-1"-yl)-3-((4- (dodecyloxy)-3-fluorophenyl)sulfonyl)-6- (methylsulfinyl)quinoline --- -- -uo                             o k O     -n 1"-(3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl)-6- (methylsulfinyl)quinolin-4-yl)-[1,4':1',4"-terpiperidin]-3-ol2020365108   27 Aug 2026Structure Name U. O ,- •'^0' o—+ \ 2-(4-(1-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6- (methylsulfmyl)qumolm-4-yl)piperidm-4-yl)piperazin-1 -yl)ethanol ,Vo ¢-00-0 tf o 4-([1,4':1',4"-terpiperidin]-1"-yl)-3-((3-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline \ + < / 1-0 I Xc < ■- Q 1''-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)-[1,4':r,4"-terpiperidin]-3-ol 0 0 .5,    oV / SC / O / F N        0    X / \O \O \O^ \ 2-(4-(1'-(3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl)-6- (methylsulfmyl)qumolm-4-yl)-[1,4‘- bipiperidin]-4-yl)piperazin-1-yl)ethanol \ + < / 1-0 I •4oooJ rf O     -n 2-(4-(1'-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)-[1,4‘-bipiperidin]-4-yl)piperazin-1-yl)ethanol o c... O    -n 3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name \ 1- co—o I ’S^OOO- Q     -n 3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline OH 0 0 ?-            zO ’Wtt 1"-(3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl)-6- (methylsulfinyl)quinolin-4-yl)-[1,4':1',4"-terpiperidin]-4-ol \ + co—O ^cyoo? O     -n 1''-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4':1',4"-terpiperidin]-4-ol o .-Q — co + \ 1''-(3-((4-(dodecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4':1',4"-terpiperidin]-4-ol \ + co-O , \~^yzCk€y° ' o 1"-(6-(methylsulfinyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinolin- 4-yl)-[1,4':1‘,4"-terpiperidin]-4-ol HO^^ 0 N ?’ 0°xzO ’WUh 2-(4-(1-(3-((4- (hexadecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethanol2020365108   27 Aug 2026Structure Name + CO —Q 0° 4-([1,4':1',4"-terpiperidin]-1"-yl)-3-((4-(hexadecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline \ + tn —O । 8^->q o 1''-(3-((4- (hexadecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4':1',4"-terpiperidin]-3-ol O    —N  O II                            1             H \ 00     A. .S. N     II               "  Il  ^1 1 IX J °IX 3-((4-methoxyphenyl)sulfonyl)-N,N-dimethyl-4-(4-methyl- 1,4-diazepan-1 -yl)quinoline-6-carboxamide 4-v-3 XX^XX V° 0" o s0 2-(4-(1-(6-(methylsulfinyl)-3-((4-(undecyloxy)phenyl)sulfonyl)quinolin-4-yl)piperidin-4-yl)piperazin-1 -yl)ethanol + tn—O ! 30^^^ cT o =0 4-([1,4':1',4"-terpiperidin]-1"-yl)-6- (methylsulfinyl)-3-((4- (undecyloxy)phenyl)sulfonyl)quinoline2020365108   27 Aug 2026Structure Name OH A 0 6 1"-(6-(methylsulfinyl)-3-((4- V 6 (undecyloxy)phenyl)sulfonyl)quinolin-4-yl)-[1,4':1',4"-terpiperidin]-4-ol 0 1 7 °\z° Y T T Y J AY AA / x ,oh 6 1"-(6-(methylsulfinyl)-3-((4- N A (undecyloxy)phenyl)sulfonyl)quinolin-4- o yl)-[1,4':1',4"-terpiperidin]-3-ol 0 1 / S. ? °\ / ° -aaUasXa Y T T Y J Av aa A'B- 0 A 2-(4-((4-([1,4': r,4"-terpiperidm]-1"-yl)-6- A (methylsulfmyl)qumolm-3-yl) sulfonyl)phenoxy) -N,N - 0 1 + Il I A / ° T          ii j diethylethanamine J 1 H ^i\A aaa< A / Aa OH A A 2-(4-(1'-(3-((4- (hexadecyloxy)phenyl)sulfonyl)-6- A / 6 (methylsulfmyl)qumolm-4-yl)-[1,4'- bipiperidin]-4-yl)piperazin-1-yl)ethanol 0 i A\. 7 0 0 aaUyva + I Y J Y J \Aa / aa aH.2020365108   27 Aug 2026Structure Name \ + cn-O । S^oo-o & 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline 0 0 ?        I °\ / 0 / s              s F 2-(4-(1'-(3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)-[1,4‘-bipiperidin]-4-yl)piperazin-1-yl)ethanol 0 0 ° XX X XX m 3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline U-. fi O                                 .<n 1 O-izw 1''-(3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4':1',4"-terpiperidin]-3-ol2020365108   27 Aug 2026Structure Name 6 1 Y J T T w 4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-3-((3-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline £ U-     O \7 1 O-c^ + \ 3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline \ 0 0 ?       T °x / ° / s x^xvA / s \ / % / F XX X XX -H N        0<£ 3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methyl- 1,4-diazepan-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline +^J0-O I x° tf° O -n £ 4-(1'-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4'-bipiperidin]-4-yl)morpholine2020365108   27 Aug 2026Structure Name yi —o । Ur cr O -n £ 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline c °’               n F zR / ^lX / L +XXJ Ur N          0\ > ' 13 3-((2-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline 0 0 °        1 °\z° / U^URsR / ^f XXX XX h n           o\ y 1                       13 F 3-((3,5-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline LI-       O ..... o-+ 3-((2,3-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 0 0 °        I °\ / ° zRRX / Y + LA J LA h n          o\ A 17 4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline 0 0 °’ 0°x / O + lA X lA h N          O\ / ^ 17 3-((3-fluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline 0 0 °’ ^\ / ° AA J XX r n         oV A 13 4-(1'-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4'-bipiperidin]-4-yl)thiomorpholine 4- CH —O Lc^oo^ GO Y 1-(4-(1'-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinolin-4-yl)-[1,4'-bipiperidin]-4-yl)piperazin-1-yl)ethanone2020365108   27 Aug 2026Structure Name 1 A A 3-((3-fluoro-4- 0 A (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- Cl / ° u 7 °\ / ° \AAsA^ F 1'-yl)-6-(methylsulfonyl)quinoline Y A A A A^ ^oH 13 n^0H A (S)-1''-(3-((4- A (dodecyloxy)phenyl)sulfonyl)-6-((S)- methylsulfinyl)quinolin-4-yl)-[1,4':1',4"- 0“ A / / / ^ + Il I A A AA5^^ A A terpiperidin]-3-ol H J \ [I A A =AqAK 11 n„0H ^lA A (S)-1''-(3-((4- A (dodecyloxy)phenyl)sulfonyl)-6-((R)- methylsulfinyl)quinolin-4-yl)-[1,4':1',4"- 0“ ! / -s\^ + Il I A / ° 'YysA^ J T H terpiperidin]-3-ol |l J \         [1 X^'N'^   A^ A0Ak 11 za*oh KrA A (R)-1''-(3-((4- ^iA A (dodecyloxy)phenyl)sulfonyl)-6-((S)- methylsulfinyl)quinolin-4-yl)-[1,4':1',4"- 0“ A ^ / --¾ + Il I A / ° vVsA^ A T H terpiperidin]-3-ol |l J \         [1 X^'N'^   A^ A0Ak 112020365108   27 Aug 2026Structure Name oh A (R)-1''-(3-((4- A (dodecyloxy)phenyl)sulfonyl)-6-((R)- methylsulfinyl)quinolin-4-yl)-[1,4':1',4"- 0 V \N / 0 terpiperidin]-3-ol / s\ |A A>V^ iiT X A 11 HO^ A A 6 (R)-2-(4-(1'-(3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl)-6- A (methylsulfinyl)quinolin-4-yl)-[1,4‘- 0“ I 0 A>^ 11 IA F bipiperidin]-4-yl)piperazin-1-yl)ethanol 'A ii H0X A ^a 6 (S)-2-(4-(1'-(3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl)-6- A (methylsulfinyl)quinolin-4-yl)-[1,4‘- 0“ A" 0 ? °x / ° Aaya^ iin F bipiperidin]-4-yl)piperazin-1-yl)ethanol ii A d (R)-2-(4-(1'-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6- N (methylsulfinyl)quinolin-4-yl)-[1,4‘- 0“ ! [A A^3.,0 AaA^ I I T F bipiperidin]-4-yl)piperazin-1-yl)ethanol 132020365108   27 Aug 2026Structure Name fl N 0 . O'. S                                   F lJX j      >< N          0^ 13 (S)-2-(4-(1'-(3-((3-fluoro-4- (tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfmyl)qumolm-4-yl)-[1,4‘-bipiperidin]-4-yl)piperazin-1-yl)ethanol U-     O ..... o—+ 3-((4-(dodecyloxy)-3- fluorophenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline 0 0' : i. / S         s C^x / F lJI J      >< N           O< 7^ 3-((4-(dodecyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name An—O on cf O -n £ 3-((4-(dodecyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline 0 N 0 : it + I J J I J 4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-3-((3-fluoro-4-(hexadecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 0 : A- XX J xx N           0< 3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 7’ U-     O GO / \ / \ / \ / —Z\ / —z   z—\ / Z—\ 'o—+ 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4-(hexadecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline + CH —O H / )—                  Z— / / \ / \ / \__ / ' \ / / ° (✓> ^-F° "" 3-((4-(dodecyloxy)-2,3- difluorophenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline u-u~> /  \ /  \ /  \ / — Z\   / Z—\   / Z—\   / Z—\ / H o—+ 3-((4-(dodecyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 20263-((4-(dodecyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1-yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline3-((4-(dodecyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-(1-ethylpiperidin-4-yl)piperazin-1-yl)piperidin-1-yl)-6-(methylsulfinyl)quinoline3-((2,3-difluoro-4-(tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1-yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 0 °' .□ ! S         / k        / k F XXX XX M XX^iX XX^oXK 3-((2,3-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline X U-     O (Z> / \ / \ / \ O / — Z\ / — Z\   / Z—\   / Z — \ / Z o—+ 3-((2,3-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (methylsulfinyl)quinoline U-     O CC / \ / \ / \ / r^ —z z—6 z—6 z—X z o—+ 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name U-     O 1 / ) / \ / \ / \ O / — Z\   / Z—\   / Z—\   / Z—\ / Z o—+ 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline + cn—O 8a>ooj ( / ) O     -n 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline U- CO / \ / \ / \ / — Z\ / — H\ / Z—\ / Z—\ / Z o—+ 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name u- <Z) / \ / \ / \ / r^ —z z—( z—( z—( / z o—+ 3-((4-(dodecyloxy)-3,5- difluorophenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline U- <Z) _  _ _oz / y^ / \ / \ \ / / ^. / — Z\ / Z —\ / Z—\ / Z—\ / Z o—+ 3-((4-(dodecyloxy)-3,5-difluorophenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline 0 0 , ¢,,. s         .A               F +YXj XT m F 3-((4-(dodecyloxy)-3,5-difluorophenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name Q 0 ? ¢, lXC X lXC >a F 3-((4-(dodecyloxy)-3,5-difluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline u- X l / > / \ / \ / \ / — Z\   / Z—\ / H—\   / Z—\   / Z O—^n + 3-((3,5-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline + i / i—o x \ / / ° Ln __ / xo O     -n 3-((3,5-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name Q 0 ? ¢, lXC X lXC yr N    y o<Y F 3-((3,5-difluoro-4- (tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (methylsulfinyl)quinoline +\n — O 2  \— Z^ \-\— Z^  Z- \\ / / \ / \ / \___ / x \ / / ° (Z ^-F° O     -n 3-((3,5-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline / / U-     O CO / \ /  \ /  \ / — Z\ / Z—\ / H—\   / Z—\ / Z o—+ 3-((3,5-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 20263-((3,5-difluoro-4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1-yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline3-((3,5-difluoro-4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1-ethylpiperidin-4-yl)piperazin-1-yl)piperidin-1-yl)-6-(methylsulfinyl)quinoline3-((4-(dodecyloxy)-2-fluorophenyl)sulfonyl)-4-(4-(4-methylpiperazin-1-yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name / \ / \ / \ o / — Z\ / Z —\ / Z—\ / H—\ / H o—+ 3-((4-(dodecyloxy)-2- fluorophenyl)sulfonyl)-4-(4-(4- ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfmyl)qumolme XGYYYXb O—to + 3-((4-(dodecyloxy)-2-fluorophenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)quinoline Q 0 ?’   Y' ,° 1 s        / k      .X *Y Y j YY w XX'-pX XX^oXK 3-((4-(dodecyloxy)-2-fluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 20264-(4-(4-ethylpiperazin-1-yl)-[1,4'-bipiperidin]-1'-yl)-3-((2-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline3-((2-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1-yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline4-(4-(4-(1-ethylpiperidin-4-yl)piperazin-1-yl)piperidin-1-yl)-3-((2-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 0 6 °’ 'tL , ! S / - Xi- / SC X XXX XX « X^-N^ XX^oXK 3-((2-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline + CH —O H  \— Z^  \—   \— Z.   Z — \\ / / \ / \ / \___ / x \ / / ° o 4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-3-((2-fluoro-4-(hexadecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline +\n — O vXvXvXOX x \ / / ° CH o 3-((2-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 0s o co / \ / \ / \ / — Z\ / — Z\ / Z —\ / Z —\ / Z o—+ 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((2-fluoro-4-(hexadecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline + cn — o \ / / co ^-F° O     -H 0 4-([1,4':1',4"-terpiperidin]-1"-yl)-3-((4-(dodecyloxy)-2,3- difluorophenyl)sulfonyl)-6-(methylsulfinyl)quinoline .0 CO / \ / \ / \ / r^ / — H\ / Z —\ / H—\ / Z —\ / Z o—+ 3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-r-yl)-6-(methylsulfmyl)quinolme2020365108   27 Aug 2026Structure Name + cn —O x \ / / ° On 0^ 3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4‘-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline + on —O H  \— Z^  \— Z.  \— Z.   Z — \\ / / \ / \ / \__ / x \ / / ° On 0 o 4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinoline 0= o .0 CO o—+ 4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (tetradecyloxy)phenyl)sulfonyl)quinoline2020365108   27 Aug 2026Structure Name 1 0 0 s       0. 0S\ * TXT Yj. « (R)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline + < / !■ iO H   \-Z^ \-Z^ \-Z.    Z- \\ / / \ / \ / \__ / x \ / / ° IO 0 (S)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline +\h-«O Z^  \-Z^  \-Z^  \-Z^   z- \\   / / \    /   \    /   \___ / x \ / / ° IO 0 (R)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline2020365108   27 Aug 2026Structure Name + ov lO H  \— Z^  \— Z.  \— Z.   Z — w / / \ / \ / \__ / x \ / / ° CH (S)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline +\n-«O z / )—    \— Z \— Z   Z-<^\ \\ / / \ / \ / \___ / \ / / ° Un 0° (R)-4-(4-(4-cyclopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline + CH- 1 O 2   \— "Z.   \— Z.   \— Z.   \Z- \\ / / \ / \ / \___ / x \ / / ° CH 0^ (S)-4-(4-(4-cyclopropylpiperazin-1 -yl)-[ 1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline2020365108   27 Aug 2026Structure Name p o ,0 -oo<0g O—^n + 3-((4-(icosyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline o .0 CO / \ / \ / \ / — H\ / Z —\ / H—\ / Z —\ / Z o—+ 4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-3-((4- (icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline o .0 CO / \ / \ / \ / r^ / — H\ / Z —\ / H—\ / Z —\ / Z o**^> + (R)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-3-((4-(icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 0’ o .0 CO / \ / \ / \ / — Z\ / Z—\ / Z—\ / Z—\ / H Oi ■ + (S)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-3-((4-(icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline + cn —O 2  \—z  \—z  \—Z  \z— \\ / / \ / \ / \___ / ' \ / / ° 9 o 0 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfinyl)quinoline +\n —O H    \\---Z.    \--Z.     Z-- \\ / / \ / \ / \___ / x \ / / ° to 0% 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name + on^O H  \— Z^  \— Z.  \— Z.   Z — \\ / / \ / \ / \__ / x \ / / ° On (R)-3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)quinoline + on- iO Z^ \— Z.   \— Z.   \— Z.   Z — \\ 0   \ /   \ /   \__ / x \ / / ° On 0^ (S)-3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)quinoline 6 0 ^0u ! 5    / ¾. .A 0S0 0. F * lXj lX « (R)-3-((4-(dodecyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name + t / )' IQ "° (S)-3-((4-(dodecyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline 0= LI-      O .0 / \ / \ / \ / r^. / -Z\ / H- / Z- / Z 1 o ► + (R)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-3-((3-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline + 0T 1O 1 Z \—~Z \—Z^ \—Z— / \\ / / \ / \ / \___ / €0 O     -n / / (S)-4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-3-((3-fluoro-4-(tetradecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 0 0 XXX XX M xxN / xx^oXK (R)-3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)quinoline + CD- IQ 5^>oo^ CD p (S)-3-((4-(dodecyloxy)phenyl)sulfonyl)-4-(4-(4-isopropylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)quinoline X-.Q I Z \— z^ \— z^ \— Z^ \z — ' / \ / \ / \ / x° O     -n X (R)-3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name U-     o .0 _ oA / \ / \ / \ / r^ —z z—f z—f z—( / z 1 O' 'i / i + (S)-3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)-6-(methylsulfinyl)quinoline 0 x0x0.~.. *XXJ XXa 17 (R)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline + l / X IQ 2       \—\—z A \ /  \ /  \ / '--\ O -- -- -- 0° (S)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (octadecyloxy)phenyl)sulfonyl)quinoline2020365108   27 Aug 2026Structure Name 0 6 °        y 0 0 +XXj IXh 11 (R)-4-([1,4‘: 1',4"-terpiperidin]-1"-yl)-3- ((4-(dodecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline 0 0 °’ Oox / o +XX X XX h N          0\ > 11 (S)-4-([1,4': 1',4"-terpiperidin]-1"-yl)-3- ((4-(dodecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline 6 6 6 7 °\ / ° XXN^ XAo-3~ 15 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylthio)quinoline2020365108   27 Aug 2026Structure Name c 0 XxX 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfonyl)quinoline + on —O H  \—Z^ \—Z.   Z— /  Z— \\ / / \ / \___ / \ / ' \ / / ° On 0^ o 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-3-((4- (icosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline + on —O Z^ \— Z^ \— Z^  Z — /  Z — \\ / / \ / \___ / \ / x \ / / ° On 0^ 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name + cn-«O H  \-Z  \-Z   Z- /  Z- / \\ / / \ / \__ / \ / ' \ / / ° On 0^ o (R)-4-(4-(4-(1-ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1-yl)-3-((4-(icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline + on. lO 2  \—Z^  \—Z.   Z— /  Z— / \\ / / \ / \__ / \ / x \ / / ° On 0 o (S)-4-(4-(4-(1-ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1-yl)-3-((4-(icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline 0 s       J. ^5' * l X J XX « X~X\OXX (R)-3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 0 o 05 O' 'tn + (S)-3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline + on —O in 0' 0 »0 4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6-(methylsulfinyl)-3-((4- (tetracosyloxy)phenyl)sulfonyl)quinoline £ 0 05 ^OO<0g O—m + 4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)-3- ((4- (tetracosyloxy)phenyl)sulfonyl)quinoline2020365108   27 Aug 2026Structure Name + on —O \ / / Ln <p o 4-(4-(4-ethylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-3-((4- (hexacosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline + on —O Q0{>0<}J \ / / Ln C0 o 4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3-((4-(hexacosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline 0s o fOO<0g o—+ 3-((4-(icosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)-4-(4-(4-propylpiperazin- 1 -yl)-[1,4'-bipiperidin]-1'-yl)quinoline2020365108   27 Aug 2026Structure Name o o—+ 4-(4-(4-butylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-3-((4- (icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline £ o o—+ 3-((4-(docosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)-4-(4-(4-propylpiperazin-1 -yl)-[1,4'-bipiperidin]-1'-yl)quinoline £ o ^OOO^ o—+ 4-(4-(4-butylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-3-((4- (docosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 1 n 0 / s            s ^Au 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylthio)quinoline \ / / ° CH / X° Z  \ Z^ \-\ z / / \ / \ / \__ / x   \ / / ° CH 0 3-((4-(hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-methylpiperazin-1 -yl)-[1,4'-bipiperidin]- 1'-yl)-6- (methylsulfonyl)quinoline 0= o .0 CH / \ / \ / \ / r^ / — z^ y— cn 4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3-((4-(hexadecyloxy)phenyl)sulfonyl)-6- (methylthio)quinoline2020365108   27 Aug 2026Structure Name jn-O ! H  \-Z  \-Z   Z- /  Z- / \\   / / \ / \__ / \ / ' \ / / ° On o 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-3-((4-(hexadecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline H  \-Z  \-Z   Z- /  Z- / \\ / / \ / \___ / \ / \ / / ° On 0^ o 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-3-((4-(hexadecyloxy)phenyl)sulfonyl)-6- methoxyquinoline 05 o \ O u_ 4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin- 1 -yl)piperidin-1 -yl)-3-((4-(hexadecyloxy)phenyl)sulfonyl)-6- (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name 0 N 6 7 °x / ° / s s       / F LXn^ LAotK 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline 0s U-     O .0 CO / \ / \ / \ / — Z\ / — Z\ / Z —\ / Z —\ / H 1 O-co + 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4-(hexadecyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline U-.0 CO / \ / \ / \ / r^ / — H\ / — H\ / H—\ / Z —\ / H O\ 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4- (hexadecyloxy)phenyl)sulfonyl)-6-methoxyquinoline2020365108   27 Aug 2026Structure Name £ U- O 03 o \ O u_ 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4-(hexadecyloxy)phenyl)sulfonyl)-6- (trifluoromethoxy)quinoline .0 CD rc / o<2-b on 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-6-(methylthio)-3-((4-(octadecyloxy)phenyl)sulfonyl)quinoline \y>-o , Z    / )-Z   \-\Z- /  \Z- / 0   / /   \   /   \__ /   \   / \ / / ° (✓> 0 7^" 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)-3- ((4- (octadecyloxy)phenyl)sulfonyl)quinoline2020365108   27 Aug 2026Structure Name H  \-Z  \-Z   Z- /  Z- / \\ / / \ / \__ / \ / ' \ / / ° On 0^ 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-6-methoxy-3-((4-(octadecyloxy)phenyl)sulfonyl)quinoline 05 ^O<0g o \ O u_ 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-3-((4-(octadecyloxy)phenyl)sulfonyl)-6- (trifluoromethoxy)quinoline u-.0 CD co 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4-(octadecyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline2020365108   27 Aug 2026Structure Name u- CO /  \ /  \ /  \ / — Z\   / — Z\   / Z —\   / Z —\ / H 1 O-co + 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4-(octadecyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline H  \-Z  \-Z   Z- /  Z- / \\ / / \ / \___ / \ / \ / / ° to "H 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4- (octadecyloxy)phenyl)sulfonyl)-6-methoxyquinoline u- o \ O u_ 4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4-(octadecyloxy)phenyl)sulfonyl)-6-methoxyquinoline2020365108   27 Aug 2026Structure Name 0 N 6 7 On / ° XAqHn 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-3-((4-(icosyloxy)phenyl)sulfonyl)-6- (methylthio)quinoline 0’ o .0 CO / \ / \ / \ / / ^ / — Z\ / — Z\ / Z —\ / Z —\ / H 1 O-co + 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-3-((4- (icosyloxy)phenyl)sulfonyl)-6- (methylsulfinyl)quinoline \> Z    / )—Z^ \-Z^ \Z— /  \Z- / \\ / / \ / \___ / \ / N \ / / ° (✓> 0' o 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm- 1 -yl)piperidin-1 -yl)-3-((4-(icosyloxy)phenyl)sulfonyl)-6- methoxyquinoline2020365108   27 Aug 20264-(4-(4-(1-ethylpiperidin-4-yl)piperazin-1-yl)piperidin-1-yl)-3-((4-(icosyloxy)phenyl)sulfonyl)-6-(trifluoromethoxy)quinoline4-(4-(4-(1-ethylpiperidin-4-yl)piperazin-1-yl)piperidin-1-yl)-3-((3-fluoro-4-(icosyloxy)phenyl)sulfonyl)-6-(methylthio)quinoline4-(4-(4-(1-ethylpiperidin-4-yl)piperazin-1-yl)piperidin-1-yl)-3-((3-fluoro-4-(icosyloxy)phenyl)sulfonyl)-6-(methylsulfinyl)quinoline2020365108   27 Aug 2026Structure Name 0’ U-     O 1 / ) / \ / \ / \   z?3\ / — Z\ / — Z\ / Z—\ / Z — \ / H O\ 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4- (icosyloxy)phenyl)sulfonyl)-6-methoxyquinoline U-     O o \ O u_ 4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-3-((3-fluoro-4-(icosyloxy)phenyl)sulfonyl)-6- (trifluoromethoxy)quinoline .0 cf) 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (methylthio)quinoline2020365108   27 Aug 2026Structure Name jn-O ! H  \-Z  \-Z   Z- /  Z- / \\   / / \ / \__ / \ / ' \ / / ° On 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (methylsulfinyl)quinoline H  \-Z  \-Z   Z- /  Z- / \\ 0   \   /   \__ /   \   / \ / / ° On 0^ 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-methoxyquinoline 05 o \ O u_ 3-((4-(docosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name 0 N 6 7 On / ° / S              S F 3-((4-(docosyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylthio)quinoline u- .u CO / \ / \ / \ / — Z\ / — Z\ / Z —\ / Z —\ / H 1 O-co + 3-((4-(docosyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-(methylsulfinyl)quinoline u- .y CO / \ / \ / \ / r^ / — H\ / — H\ / H—\ / Z —\ / H O\ 3-((4-(docosyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-methoxyquinoline2020365108   27 Aug 2026Structure Name Q 0 6 ? / ° F3C XXCJ XX x 3-((4-(docosyloxy)-3-fluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-(trifluoromethoxy)quinoline uT^ n \ O XoO<D^ \ 1 / ) _^ / MX O     -n 3-((4-(docosyloxy)-3,5-difluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline UJ1"1 n \ o \ / / (Z> x 3-((4-(docosyloxy)-2,3-difluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name OJ1”1 O \ o V o 3-((4-(docosyloxy)-2-fluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-(trifluoromethoxy)quinoline 0 ¢) 6 ? °\ / ° FsC XXX XXm F 3-((3,5-difluoro-4- (icosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline UJ1"1 n \ o Xooo^ \ (Z> O     -n to'T^' 3-((2,3-difluoro-4-(icosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name OJ1”1 O \ o is> o .7 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((2-fluoro-4-(icosyloxy)phenyl)sulfonyl)-6- (trifluoromethoxy)quinoline C 6 ? °\ / ° ^0.        A.              _F FsC XXX XXm F 3-((3,5-difluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline UJ1"1 n \ o Xooo^ V 3-((2,3-difluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name OJ1”1 O \ o is> o 4-(4-(4-(1 -ethylpiperidm-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((2-fluoro-4-(octadecyloxy)phenyl)sulfonyl)-6- (trifluoromethoxy)quinoline uT^ n \ O Q;2OO<D^ \ 1 / ) O     -n 3-((3,5-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline UJ1"1 n \ o Q;OO<Dz7 \ (Z> 3-((2,3-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name £ _ o \ o | ,(-0 4-(4-(4-(1 -ethylpiperidin-4-yl)piperazm-1 -yl)piperidin-1 -yl)-3-((2-fluoro-4-(hexadecyloxy)phenyl)sulfonyl)-6- (trifluoromethoxy)quinoline n \ O \ ■n o 5£ 3-((2,6-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline A<>o<Jy o \ o co 3-((2,6-difluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name u7 n \ O QkXXP o A 3-((2,6-difluoro-4- (icosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 - yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline uT n \ O Q;OO<DzJ V ^o o A 3-((4-(docosyloxy)-2,6-difluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline k 0 N k . ? °\ / ° / k ksk F3C TXj XX >4 F 3-((2,5-difluoro-4- (hexadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline2020365108   27 Aug 2026Structure Name J1 n \ O <Z) o 3-((2,5-difluoro-4- (octadecyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline £ o KHK^ o \ o m 3-((2,5-difluoro-4-(icosyloxy)phenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6- (trifluoromethoxy)quinoline and J1 o \ O \ tn o £ 3-((4-(docosyloxy)-2,5-difluorophenyl)sulfonyl)-4-(4-(4-(1 -ethylpiperidin-4-yl)piperazin-1 -yl)piperidin-1 -yl)-6-(trifluoromethoxy)quinoline.

19. A pharmaceutical composition comprising a compound of any one of claims 5-18 or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or tautomer thereof;optionally wherein the pharmaceutical composition is for parenteral administration; and / or2020365108   27 Aug 2026optionally wherein the compound is a pharmaceutically acceptable salt.

20. A method of agonizing Pigment-Epithelium-Derived Factor (PEDF) receptors in a subject in need thereof, comprising administering to the patient an effective amount of a compound of any one of claims 5-18 or a pharmaceutical composition of claim 19.

21. A method of inhibiting angiogenesis in a subject in need thereof, comprising administering to the patient an effective amount of a compound of any one of claims 5-18 or a pharmaceutical composition of claim 19,optionally wherein the angiogenesis is pathogenic angiogenesis.

22. A method of treating a pathogenic blood vessel-related disorder in a subject in need thereof, comprising administering to the patient an effective amount of a compound of any one of claims 5-18 or a pharmaceutical composition of claim 19,optionally wherein the patient has a disease or disorder selected from a cancer, retinal occlusive vascular disease, retinopathy of prematurity, diabetic retinopathy, and age-related macular degeneration.

23. A method of treating a cancer in a subject in need thereof, comprising administering to the patient an effective amount of a compound of any one of claims 5-18 or a pharmaceutical composition of claim 19,optionally wherein the cancer is selected from the group consisting of colon cancer, breast cancer, prostate cancer, lung cancer, liver cancer, pancreatic cancer, ovarian cancer, bladder cancer, kidney cancer, esophageal cancer, cervical cancer, endometrial cancer, melanoma, brain cancer, glioma, neuroblastoma, osteosarcoma, chondrosarcoma, gastric carcinoma, mesothelioma, Kaposi sarcoma, liposarcoma, synovial sarcoma, or Wilm’s tumor.

24. A method of treating retinal occlusive vascular disease, retinopathy of prematurity, diabetic retinopathy, or age-related macular degeneration in a subject in need thereof, comprising administering to the patient an effective amount of a compound of any one of claims 5-18 or a pharmaceutical composition of claim 19.

Images