Selective CDK4 / 6 inhibitor cancer treatment

Abstract

The present disclosure describes embodiments of selective and potent CDK4 / 6 inhibitors that advantageously inhibit cancer growth even at low concentrations. As described herein, the compounds of this approach include substituted pyridinylpiperazine-pyrrolepyrimidine compounds having a fatty acid moiety. The compounds described herein can be used as pharmaceutical compounds for anticancer therapy and are useful in the treatment, prevention, and / or amelioration of cancer.

Description

[Technical Field]

[0001] The present disclosure relates to pharmaceutical compositions for anti-cancer therapy, and more particularly to substituted pyridinylpiperazine-pyrrolepyrimidine compounds that are potent CDK4 / 6 inhibitors and may also be used in the treatment, prevention and / or amelioration of cancer. [Background technology]

[0002] Cancer stem cells (CSCs) are tumor-initiating cells (TICs) that are resistant to conventional cancer therapies, such as chemotherapy and radiation therapy. As a result, CSCs contribute to both tumor recurrence and distant metastasis, leading to treatment failure and poor clinical outcomes in cancer patients. Therefore, inventive methods require understanding how to address the issue of CSCs. Mechanistically, this may relate to the ability of CSCs to survive and grow under harsh conditions and different microenvironments. Because CSCs represent a particularly small subset of the tumor cell population, their metabolic and phenotypic properties remain largely uncharacterized to date.

[0003] Furthermore, CSCs exhibit remarkable resilience and resistance to cellular stress, allowing them to grow anchorage-independently, especially under low-adhesion conditions. Consequently, they form 3D spheroids, retaining the properties of CSCs and stem / progenitor cells. On the other hand, when grown in suspension, many "bulk" cancer cells die by anoikis, a specialized form of apoptosis. Therefore, clonal expansion of a single CSC leads to the production of 3D spheroids, preventing cancer cell self-aggregation. Consequently, 3D spheroid formation is a functional readout of stemness in epithelial cancer cells, resulting in an enriched population of epithelioid cells with a stem-like phenotype. These 3D spheroids are also known as tumor-like masses, especially when prepared using breast cancer cells such as MCF7.

[0004] Previously, 3D spheroids were generated from two different ER(+) cell lines (MCF7 and T47D) and subjected to comprehensive label-free proteomic analysis. This study aimed to analyze the phenotypic behavior of CSCs at the molecular level. 3D spheroids were directly compared with monolayers of these cell lines and processed in parallel. This allowed for the identification of proteomic signatures specific to the CSC phenotype in 3D spheroids compared to monolayers. Based on this molecular analysis, tumor-like masses were observed to be significantly enriched in mitochondrial proteins. These mitochondria-associated proteins included molecules involved in β-oxidation and ketone metabolism / recycling, mitochondrial biogenesis, electron transport, ADP / ATP exchange / transport, CoQ synthesis and ROS production, and mitophagy inhibition. Thus, increased mitochondrial protein synthesis or decreased mitophagy led to the accumulation of mitochondrial mass in CSCs.

[0005] Given the increased CSC activity, mitochondrial mass has been considered a novel metabolic biomarker for eliminating CSCs. Using this general approach, we observed that CSC activity could be significantly enhanced using only MitoTracker as a marker in ER(+) (MCF7) and ER(-) (MDA-MB-231) breast cancer cell lines. Surprisingly, cells with high MitoTracker levels were found to be chemoresistant to paclitaxel and resistant to the paclitaxel-induced DNA damage response.

[0006] However, what is needed are novel pharmaceutical compounds for anti-cancer therapies that eradicate CSCs, prevent or reduce the likelihood of metastasis and / or recurrence, and reduce or eliminate cancers that are resistant to chemotherapy and other anti-cancer therapies. Additionally, what is needed are treatment strategies and anti-cancer therapies that specifically target "optimal" CSCs and eliminate further cancer growth, including anchorage-independent growth, tumor recurrence, and distant metastasis. [Prior art documents] [Patent documents]

[0007] [Patent Document 1] U.S. Patent No. 8,598,197 Summary of the Invention [Problem to be solved by the invention]

[0008] Cancer stem cells (CSCs) are currently considered to be one of the major underlying causes of treatment failure in cancer patients worldwide. Mechanistically, this may be related to the survival and growth capacity of CSCs under harsh conditions and different microenvironments. The inventors proposed a theory that CSCs become resistant to conventional therapies by using elevated mitochondrial OXPHOS metabolism to "high-energy" ATP production. Consistent with this view, various mitochondrial inhibitors, including i) FDA-approved antibiotics (doxycycline, tigecycline, azithromycin, pyrvinium pamoate, atovaquone, and bedaquiline), ii) natural compounds (actinonin, CAPE, berberine, brutieridine, and melitidine), and iii) experimental compounds (oligomycin and the MCT1 / 2 inhibitor AR-C155858), successfully blocked 3D tumorsphere formation. [Means for solving the problem]

[0009] Cyclin-dependent kinases (CDKs) 4 and 6 are enzymes known to promote mitosis and meiosis in both normal and cancer cells. These enzymes phosphorylate and inactivate the retinoblastoma protein, which plays a role in cell cycle progression from the G1 to S phase. Studies have identified abnormalities in cancer cells that increase CDK activity. This increased activity leads to the inactivation of various tumor suppressor genes, facilitating rapid cancer stem cell proliferation and tumor growth. Naturally occurring CDK protein inhibitors, such as p16 and p27, have been shown to inhibit the growth of lung cancer cell lines in vitro. Certain CDK inhibitors may be useful as chemopreventive agents due to their ability to inhibit cell cycle progression in normal, non-transformed cells.

[0010] Targeted inhibition of these enzymes, alone or in combination with other therapies, represents a potential avenue for anti-cancer treatment and therapeutic agents. Blocking the CDK4 / 6 pathway prevents cells from progressing through S phase, achieving cell death by apoptosis. Described herein are embodiments of pyrrole-pyrimidine compounds that are CDK inhibitors, primarily inhibitors of CDK4 and CDK6 ("CDK4 / 6"), that have potent efficacy as cancer therapeutics. More specifically, embodiments of anti-cancer CDK4 / 6 inhibitors according to this approach are substituted pyridinylpiperazine-pyrrole-pyrimidine compounds bearing a fatty acid moiety. The compounds shown below are compounds in which m is an integer between 0 and 4, more preferably between 0 and 2, and n is an integer between 0 and 2. 12 and n is an integer of 1 to 22, more preferably an integer of 12 to 20, and some embodiments of the first anticancer CDK4 / 6 inhibitor are described.

[0011] [ka]

[0012] m is 0 and n is 12 The following compound, wherein: is an illustrative embodiment of the pyridinylpiperazine-pyrrolepyrimidine anti-cancer CDK4 / 6 inhibitors described herein.

[0013] [ka]

[0014] The compound shown below is another exemplary embodiment of a substituted pyridinylpiperazine-pyrrolepyrimidine compound according to this approach. In this embodiment, "m" is 2 and "n" is 14.

[0015] [ka]

[0016] The compounds described herein, including their salts, can be used as pharmaceutical compounds for the treatment of cancer. The present method also provides pharmaceutical formulations having a therapeutically effective amount of the compound or a therapeutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent, or excipient thereof. All of these forms are encompassed by the present method. It will be understood that pharmaceutically acceptable carriers can be used as known in the art.

[0017] The compounds described herein can be used in connection with a method for treating cancer in a mammal, including a human, comprising administering to the mammal an amount of a substituted pyridinylpiperazine-pyrrolepyrimidine compound, or a pharmaceutically acceptable salt thereof, effective to treat the disorder or condition. For example, this approach is useful for treating abnormal cell growth, such as cancer. The compounds described herein can be used to treat abnormal cell proliferative disorders, particularly cancers selected from the group consisting of cancers of the breast, ovary, cervix, prostate, testicle, esophagus, stomach, skin, lung, bone, colon, pancreas, thyroid, biliary tract, oral vestibule and pharynx (oral cavity), lips, tongue, mouth, pharynx, small intestine, colorectum, large intestine, rectum, brain and central nervous system, glioblastoma, neuroblastoma, keratoacanthoma, epidermoid carcinoma, large cell carcinoma, adenocarcinoma, adenoma, adenocarcinoma, follicular carcinoma, undifferentiated carcinoma, papillary carcinoma, seminoma, melanoma, sarcoma, bladder cancer, liver cancer, renal cancer, myeloid disorders, lymphoid disorders, Hodgkin's disease, and hairy cell leukemia, by administering a therapeutically effective amount of the first, second, or third compound, or a pharmaceutically acceptable salt thereof, to a subject diagnosed with such a cancer. In some embodiments, this approach can be used in combination with and / or to increase the effectiveness of other therapies.

[0018] Embodiments of the present approach can be recognized by those skilled in the art upon review of the following detailed description. DETAILED DESCRIPTION OF THE INVENTION

[0019] The following description includes modes currently contemplated for carrying out exemplary embodiments of the present technique. The following description is not to be taken in a limiting sense, but is made merely for the purpose of illustrating the general principles of the invention.

[0020] According to this approach, one or more substituted pyridinylpiperazine-pyrrolepyrimidine CDK4 / 6 inhibitors can be used as anti-cancer therapeutic agents. According to this approach, the pyridinylpiperazine moiety is substituted with a fatty acid moiety, preferably having at least 14 carbons, preferably 14 to 22 carbons. The compounds described herein have valuable pharmaceutical and medicinal properties. Many of the compounds exhibit significant selective CDK4 / 6 inhibitory activity and are therefore useful in treating a variety of clinical conditions in which CDK4 / 6 kinase is abnormally elevated or activated or present in normal amounts and activity, although inhibition of CDK is desirable for treating cell proliferation disorders. In particular, these compounds are promising anti-cancer therapeutic agents. Various compounds are described below under definitions and are applicable to embodiments of this approach.

[0021] As used herein, the designation C(O) refers to a carbon-oxygen double bond. As used herein, the term "halo" means halogen and includes bonded fluorine, chlorine, bromine, or iodine, as understood in the art.

[0022] As used herein, the term "alkyl" refers to saturated aliphatic groups, including straight-chain alkyl groups (e.g., methyl, ethyl, etc.), branched-chain alkyl groups (e.g., isopropyl, tert-butyl, etc.), cycloalkyl (alicyclic) groups (cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl), alkyl-substituted cycloalkyl groups, and cycloalkyl-substituted alkyl groups. The term "alkyl" also includes alkenyl and alkynyl groups. In the general formula, "C nThe term "alkyl" is sometimes used, where n is an integer, e.g., 1 to 20, to refer to a particular alkyl group (straight or branched) having a particular range or number of carbons. For example, the term C1-C3 alkyl includes, but is not limited to, methyl, ethyl, propyl, and isopropyl. Similarly, the term C3-C6 cycloalkyl includes, but is not limited to, cyclopropyl, cyclopentyl, and cyclohexyl. Alkyl and cycloalkyl groups can be unsubstituted or substituted. Thus, the term alkyl includes both "unsubstituted alkyl" and "substituted alkyl," the latter referring to moieties having substituents replacing a hydrogen on one or more carbons in the hydrocarbon backbone.

[0023] The term "alkenyl" includes unsaturated aliphatic groups analogous in length and possible substitution to the alkyls described above, but which contain at least one double bond. Alkenyl also includes "unsubstituted alkenyls" and "substituted alkenyls," the latter of which refers to moieties having substituents replacing a hydrogen on one or more carbons in the hydrocarbon backbone.

[0024] For example, the term "alkenyl" includes straight-chain alkenyl groups (e.g., ethenyl, propenyl, butenyl, pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, etc.), branched-chain alkenyl groups, cycloalkenyl (alicyclic) groups (cyclopropenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl), alkyl- or alkenyl-substituted cycloalkenyl groups, and cycloalkyl- or cycloalkenyl-substituted alkenyl groups. The term alkenyl further includes alkenyl groups which include oxygen, nitrogen, sulfur or phosphorous atoms replacing one or more carbons in the hydrocarbon backbone. In certain embodiments, a straight-chain or branched-chain alkenyl group has 6 or fewer carbon atoms in its backbone (e.g., C2-C6 for straight chain, C3-C6 for branched chain). Likewise, cycloalkenyl groups can have from 3 to 8 carbon atoms in their ring structure, and more preferably 5 or 6 carbons in the ring structure. The term C2-C6 includes alkenyl groups containing from 2 to 6 carbon atoms.

[0025] The term "alkynyl" includes unsaturated aliphatic groups analogous in length and possible substitution to the alkyls described above, but which contain at least one triple bond. Furthermore, the term alkynyl includes both "unsubstituted alkynyls" and "substituted alkynyls," the latter of which refers to alkynyl moieties having substituents replacing a hydrogen on one or more carbons in the hydrocarbon backbone.

[0026] By way of example, the term "alkynyl" includes straight-chain alkynyl groups (e.g., ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl, octynyl, nonynyl, decynyl, etc.), branched-chain alkynyl groups, and cycloalkyl- or cycloalkenyl-substituted alkynyl groups. The term alkynyl further includes alkynyl groups which include oxygen, nitrogen, sulfur, or phosphorous atoms replacing one or more carbons in the hydrocarbon backbone. In certain embodiments, a straight-chain or branched-chain alkynyl group has six or fewer carbon atoms in its backbone (e.g., C2-C6 for straight chain and C3-C6 for branched chain). The term C2-C6 includes alkynyl groups having from 2 to 6 carbon atoms.

[0027] The term "substituted" is intended to describe moieties having substituents replacing a hydrogen on one or more atoms such as C, O, or N of a molecule. Examples of such substituents include, but are not limited to, alkyl, alkoxy, alkenyl, alkynyl, halo, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, amino (including alkylamino, dialkylamino, arylamino, diarylamino, and alkylarylamino), Examples of suitable moieties include acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl, and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfate, alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, morpholino, phenol, benzyl, phenyl, piperidine, cyclopentane, cyclohexane, pyridine, 5H-tetrazole, triazole, piperidine, or aromatic or heteroaromatic moieties, and combinations thereof. Substituents for the pyridinylpiperazine moiety include fatty acid moieties, as described herein. The fatty acid moiety preferably contains at least 14 carbon atoms, and preferably contains from 14 to about 22 carbon atoms.

[0028] The term "amine" or "amino" refers to a molecule, moiety, or functional group, as commonly understood in the art, and may be primary, secondary, or tertiary. The term "amine" or "amino" includes compounds in which a nitrogen atom is covalently bonded to at least one carbon, hydrogen, or heteroatom. This term includes, for example, but is not limited to, "alkylamino," "arylamino," "diarylamino," "alkylarylamino," "alkylaminoaryl," "arylaminoalkyl," "alkaminoalkyl," "amide," "amido," and "aminocarbonyl." The term "alkylamino" includes groups and compounds in which the nitrogen is bound to at least one additional alkyl group. The term "dialkylamino" includes groups in which the nitrogen atom is bound to at least two additional alkyl groups. The terms "arylamino" and "diarylamino" include groups in which the nitrogen is bound to at least one or two aryl groups, respectively. The terms "alkylarylamino," "alkylaminoaryl," or "arylaminoalkyl" refer to an amino group bound to at least one alkyl group and at least one aryl group. The term "alkaminoalkyl" refers to an alkyl, alkenyl, or alkynyl group bound to a nitrogen atom which is also bound to an alkyl group.

[0029] The term "amide," "amido," or "aminocarbonyl" includes compounds or moieties which contain a nitrogen atom which is bound to the carbon of a carbonyl or a thiocarbonyl group. This term includes "alkaminocarbonyl" or "alkylaminocarbonyl" groups which contain alkyl, alkenyl, aryl, or alkynyl groups bound to an amino group which is bound to a carbonyl group. It also includes arylaminocarbonyl and arylcarbonylamino groups which contain aryl or heteroaryl moieties bound to an amino group which is bound to the carbon of a carbonyl or thiocarbonyl group. The terms "alkylaminocarbonyl," "alkenylaminocarbonyl," "alkynylaminocarbonyl," "arylaminocarbonyl," "alkylcarbonylamino," "alkenylcarbonylamino," "alkynylcarbonylamino," and "arylcarbonylamino" are included within the term "amide." Amides also include urea groups (aminocarbonylamino) and carbamates (oxycarbonylamino).

[0030] The term "aryl" includes groups containing 5- and 6-membered monocyclic aromatic groups, which may contain zero to four heteroatoms, such as phenyl, pyrrole, furan, thiophene, thiazole, isothiazole, imidazole, triazole, tetrazole, pyrazole, oxazole, isoxazole, pyridine, pyrazine, pyridazine, and pyrimidine. The term "aryl" also includes tricyclic, bicyclic, and other polycyclic aryl groups, such as naphthalene, benzoxazole, benzodioxazole, benzothiazole, benzimidazole, benzothiophene, methylenedioxyphenyl, quinoline, isoquinoline, anthryl, phenanthryl, naphthyridine, indole, benzofuran, purine, benzofuran, deazapurine, or indolizine. These aryl groups having heteroatoms in the ring structure may also be referred to as "aryl heterocycles," "heterocycles," "heteroaryls," or "heteroaromatics." The aromatic ring may be substituted at one or more ring positions as described above, for example, with alkyl, halogen, hydroxyl, alkoxy, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, alkylaminocarbonyl, aralkylaminocarbonyl, alkenylaminocarbonyl, alkylcarbonyl, arylcarbonyl, aralkylcarbonyl, alkenylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylthiocarbonyl, phosphate, phosphonato, phosphinato, cyano, hydroxyl ... The aryl groups can be substituted with substituents such as nitro, amino (including alkylamino, dialkylamino, arylamino, diarylamino, and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl, and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfate, alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, or aromatic or heteroaromatic moieties. Aryl groups can also be fused or bridged with alicyclic or non-aromatic heterocycles to form polycycles (e.g., tetralin).

[0031] As used herein, the term heteroaryl refers to a stable monocyclic or bicyclic ring of up to seven atoms in each ring, where at least one ring is aromatic and contains one to four heteroatoms selected from the group consisting of O, N, and S. Heteroaryl groups within this definition include, but are not limited to, acridinyl, carbazolyl, cinnolinyl, quinoxalinyl, pyrazolyl, indolyl, benzotriazolyl, furanyl, thienyl, benzothienyl, benzofuranyl, quinolinyl, isoquinolinyl, oxazolyl, isoxazolyl, indolyl, pyrazinyl, pyridazinyl, pyridinyl, pyrimidinyl, pyrrolyl, and tetrahydroquinoline. As with the definition of heterocycle below, "heteroaryl" is also understood to include the N-oxide derivative of any nitrogen-containing heteroaryl. When a heteroaryl substituent is bicyclic and one ring is non-aromatic or does not contain a heteroatom, attachment is understood to be via the aromatic ring or the heteroatom-containing ring, respectively.

[0032] As used herein, the term "heterocycle" or "heterocyclyl" is intended to mean a 5- to 10-membered aromatic or non-aromatic heterocycle containing from 1 to 4 heteroatoms selected from the group consisting of O, N, and S, including bicyclic groups. "Heterocyclyl" therefore includes the above heteroaryls, as well as dihydro and tetrahydro analogs thereof. Further examples of "heterocyclyl" include, but are not limited to, the following: benzimidazolyl, benzofuranyl, benzofurazanyl, benzopyrazolyl, benzotriazolyl, benzothiophenyl, benzoxazolyl, carbazolyl, carbolinyl, cinnolinyl, furanyl, imidazolyl, indolinyl, indolyl, indolazinyl, indazolyl, isobenzofuranyl, isoindolyl, isoquinolyl, isothiazolyl, isoxazolyl, naphthapyridinyl, oxadiazolyl, oxazolyl, oxazoline, isoxazoline, oxetanyl, pyranyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridopyridinyl, pyridazinyl, pyridyl, pyrimidyl, pyrrolyl, quinazolinyl, quinolyl, quinoxalinyl, tetrahydropyranyl, tetrazolyl, tetrazolopyridyl, thiadiazolyl, thiazolyl, thienyl, triazolyl, azetidinyl, 1 ,4-dioxanyl, hexahydroazepinyl, piperazinyl, piperidinyl, pyridin-2-onyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, dihydrobenzimidazolyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, dihydrobenzoxazolyl, dihydrofuranyl, dihydroimidazolyl, dihydroindolyl, dihydroisoxazolyl, dihydroisothiazolyl, dihydrooxadiazolyl, dihydrooxazolyl, dihydropyrazinyl, dihydropyrazolyl, dihydropyridinyl, dihydropyrimidinyl, dihydropyrrolyl, dihydroquinolinyl, dihydrotetrazolyl, dihydrothiadiazolyl, dihydrothiazolyl, dihydrothienyl, dihydrotriazolyl, dihydroazetidinyl, methylenedioxybenzoyl, tetrahydrofuranyl and tetrahydrothienyl, and N-oxides thereof. Attachment of a heterocyclyl substituent can occur via a carbon atom or via a heteroatom.

[0033] The term "acyl" includes compounds and moieties that contain the acyl radical (CH3CO-) or a carbonyl group. The term "substituted acyl" includes acyl groups in which one or more hydrogen atoms are replaced by, for example, an alkyl group, an alkynyl group, a halogen, a hydroxyl, an alkylcarbonyloxy, an arylcarbonyloxy, an alkoxycarbonyloxy, an aryloxycarbonyloxy, a carboxylate, an alkylcarbonyl, an arylcarbonyl, an alkoxycarbonyl, an aminocarbonyl, an alkylaminocarbonyl, a dialkylaminocarbonyl, an alkylthiocarbonyl, an alkoxyl, a phosphate, a phosphonato, a phosphinato, a cyano, an amino (including alkylamino, dialkylamino, arylamino, diarylamino, and alkylarylamino), an acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl, and ureido), amidino, an imino, a sulfhydryl, an alkylthio, an arylthio, a thiocarboxylate, a sulfate, an alkylsulfinyl, a sulfonato, a sulfamoyl, a sulfonamido, a nitro, a trifluoromethyl, a cyano, an azido, a heterocyclyl, an alkylaryl, or an aromatic or heteroaromatic moiety.

[0034] The term "acylamino" includes moieties in which an acyl moiety is attached to an amino group. For example, this term includes alkylcarbonylamino, arylcarbonylamino, carbamoyl, and ureido groups.

[0035] The term "alkoxy" includes substituted and unsubstituted alkyl, alkenyl, and alkynyl groups covalently linked to an oxygen atom. Examples of alkoxy groups include methoxy, ethoxy, isopropyloxy, propoxy, butoxy, and pentoxy groups, and may include cyclic groups such as cyclopentoxy. Examples of substituted alkoxy groups include halogenated alkoxy groups. Alkoxy groups can be substituted with groups such as alkenyl, alkynyl, halogen, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, cyano, amino (including alkylamino, dialkylamino, arylamino, diarylamino, and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl, and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfate, alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, or an aromatic or heteroaromatic moiety. Examples of halogen substituted alkoxy groups include, but are not limited to, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chloromethoxy, dichloromethoxy, trichloromethoxy, and the like.

[0036] The terms "carbonyl" or "carboxy" include compounds and moieties containing a carbon connected with a double bond to an oxygen atom, and tautomeric forms thereof. Examples of carbonyl-containing moieties include aldehydes, ketones, carboxylic acids such as fatty acid moieties, amides, esters, anhydrides, and the like. The terms "fatty acid moiety," "carboxy moiety," and "carbonyl moiety" refer to groups such as "alkylcarbonyl" groups in which an alkyl group is covalently bonded to a carbonyl group, "alkenylcarbonyl" groups in which an alkenyl group is covalently bonded to a carbonyl group, "alkynylcarbonyl" groups in which an alkynyl group is covalently bonded to a carbonyl group, and "arylcarbonyl" groups in which an aryl group is covalently bonded to a carbonyl group. Additionally, the terms also refer to groups in which one or more heteroatoms are covalently bonded to the carbonyl moiety. For example, this term includes moieties such as aminocarbonyl moieties (wherein the nitrogen atom is bonded to the carbonyl carbon, e.g., amides), aminocarbonyloxy moieties (e.g., also called "carbamates") in which both an oxygen and a nitrogen atom are bonded to the carbonyl carbon. Additionally, aminocarbonylamino groups (e.g., ureas) also include other combinations of carbonyl groups bonded to heteroatoms (e.g., nitrogen, oxygen, sulfur, etc., as well as carbon atoms). Furthermore, the heteroatoms can be further substituted with one or more alkyl, alkenyl, alkynyl, aryl, aralkyl, acyl, etc., moieties.

[0037] The term "thiocarbonyl" or "thiocarboxy" includes compounds and moieties which contain a carbon double bonded to a sulfur atom. The term "thiocarbonyl moiety" includes moieties which are similar to a carbonyl moiety. For example, a "thiocarbonyl" moiety includes an aminothiocarbonyl in which the amino group is bonded to the carbon atom of the thiocarbonyl group; further thiocarbonyl moieties include oxythiocarbonyl (oxygen bonded to the carbon atom), aminothiocarbonylamino, and the like.

[0038] The term "ether" includes compounds or moieties which contain an oxygen bonded to two different carbon atoms or heteroatoms. For example, this term includes "alkoxyalkyls" in which an alkyl, alkenyl, or alkynyl group is covalently bonded to an oxygen atom which is covalently bonded to another alkyl group.

[0039] The term "ester" includes compounds and moieties which contain a carbon or heteroatom bound to an oxygen atom which is bonded to the carbon of a carbonyl group. The term "ester" includes alkoxycarboxy groups such as methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, butoxycarbonyl, pentoxycarbonyl, and the like. The alkyl, alkenyl, or alkynyl groups are as defined above.

[0040] The term "thioether" includes compounds and moieties containing a sulfur atom bonded to two different carbon or heteroatoms. Examples of thioethers include, but are not limited to, alkthioalkyls, alkthioalkenyls, and alkthioalkynyls. The term "alkthioalkyls" includes compounds having an alkyl, alkenyl, or alkynyl group bonded to a sulfur atom that is bonded to an alkyl group. Similarly, the terms "alkthioalkenyl" and "alkthioalkynyl" refer to compounds or moieties in which an alkyl, alkenyl, or alkynyl group is bonded to a sulfur atom that is covalently bonded to an alkynyl group.

[0041] The term "hydroxy" or "hydroxyl" includes groups with an --OH or --O-- group.

[0042] The terms "polycyclic" or "polycyclic radical" include moieties having two or more rings (e.g., cycloalkyl, cycloalkenyl, cycloalkynyl, aryl, and / or heterocyclyl) where two or more carbons are shared between two adjacent rings. For example, these rings are "fused rings." Rings that are joined by non-adjacent atoms are referred to as "bridged" rings. Each ring of a polycyclic ring may be substituted with, for example, halogen, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl, aralkylaminocarbonyl, alkenylaminocarbonyl, alkylcarbonyl, arylcarbonyl, aralkylcarbonyl, alkenylcarbonyl, aminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, cyano, amino(alkylamino), diazoto, hydroxyl ... and the like. The amino group may be substituted as above with a substituent such as alkylamino, arylamino, diarylamino, and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl, and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfate, alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkyl, alkylaryl, or an aromatic or heteroaromatic moiety.

[0043] The term "heteroatom" includes atoms of any element other than carbon or hydrogen. Preferred heteroatoms are nitrogen, oxygen, sulfur, and phosphorus.

[0044] Furthermore, the phrase "any combination of these" indicates that any number of the listed functional groups and molecules may be combined to create a larger molecular structure. For example, "phenyl," "carbonyl" (or "=O"), "-O-," "-OH," and C 1-6(i.e., the terms -CH and -CHCHCH-) can be combined to form a 3-methoxy-4-propoxybenzoic acid substituent. It should be understood that when combining functional groups and molecules to create larger molecular architectures, hydrogens can be removed or added to satisfy the valence of each atom.

[0045] As will be understood by those skilled in the art, the compounds described herein include bonds between adjacent atoms and / or hydrogen atoms to satisfy the valence of each atom. If necessary, bonds and / or hydrogen atoms are added to provide the following total bond counts for each atomic type: carbon: 4 bonds; nitrogen: 3 bonds; oxygen: 2 bonds; and sulfur: 2-6 bonds.

[0046] As used herein, the phrase "pharmaceutically effective amount" refers to the amount that needs to be administered to a host, or to a cell, tissue, or organ of a host, to achieve a therapeutic result, such as regulating, modulating, or inhibiting protein kinase activity, e.g., inhibiting protein kinase activity, or treating cancer. A physician or veterinarian skilled in the art can readily determine and prescribe the effective amount of the pharmaceutical composition required. For example, the physician or veterinarian can start the dosage of the compound of the present invention used in the pharmaceutical composition at a lower amount than needed to achieve the desired therapeutic effect, and gradually increase the dosage until the desired effect is achieved.

[0047] The terms "treat," "treated," "treating," and "treatment" include the reduction or alleviation of at least one symptom associated with or resulting from the condition, disorder, or disease being treated, particularly cancer. In certain embodiments, treatment involves reducing or alleviating at least one symptom associated with or resulting from the cancer being treated with a compound of the invention. For example, treatment can be the reduction of one or more symptoms of cancer, or the complete eradication of cancer.

[0048] The compounds described herein contain what is also known as a carbonyl moiety, which this disclosure refers to as a fatty acid moiety. As used herein, a fatty acid is a carboxylic acid having an aliphatic chain, which may be saturated or unsaturated, although a saturated chain is preferred. An example of a saturated fatty acid is lauric acid (CH3(CH2) 10 C(O)OH), palmitic acid (CH3(CH2) 14 C(O)OH), stearic acid (CH3(CH2) 16 C(O)OH) and myristic acid (CH3(CH2) 12 Examples of fatty acid moieties include fatty acid salts or esters (CH3(CH2)7CH=CH(CH2)7C(O)OH). Oleic acid (CH3(CH2)7CH=CH(CH2)7C(O)OH) is an example of a naturally occurring unsaturated fatty acid. Although reference is made to salts or esters of fatty acids, as well as their fatty acid amide moieties, for brevity as used herein, these are included within the meaning of the fatty acid moiety. For example, myristic acid may be referred to as myristate, and oleic acid may be referred to as oleate. The fatty acid moiety may also be a carboacyl group of a fatty acid, i.e., a group formed by the loss of a hydroxide group in the carboxylic acid. In some embodiments, the fatty acid moiety may be linked to the therapeutic agent through an amide bond. As an example, a myristic acid conjugate may be linked to the fatty acid moiety CH3(CH2) 12 CO-NH-, where the tertiary nitrogen is the therapeutic agent:

[0049] [ka]

[0050] where n is an integer from 1 to 20, preferably 10 to 20. This may occur when the myristate moiety is conjugated by myristoylation, resulting in a tetradecanamide (or myristamide) group.

[0051] According to this approach, anti-cancer CDK4 / 6 inhibitors include substituted pyridinylpiperazine-pyrrolepyrimidine compounds as shown in the following general formula [1]:

[0052] [ka]

[0053] When used in general formula [1], "m" in the fatty acid moiety is an integer of 0 to 4, more preferably 0 to 2, and when m is 0, it is directly bonded to the nitrogen of the piperazine; "n" in the fatty acid moiety is an integer of 13 to 22, preferably 14 to 20, and may be 14, 15, 16, 17, 18, 19, 20, 21, or 22, and is preferably saturated and linear; R 1 is selected from the group consisting of hydrogen, C1-C8 alkyl, substituted C1-C8 alkyl, C3-C8 cycloalkyl, substituted C3-C8 cycloalkyl, aryl, substituted aryl, heteroaryl and substituted heteroaryl, halo-substituted alkoxy groups.

[0054] In one preferred embodiment of this approach, the anti-cancer CDK4 / 6 inhibitor has the following formula [2]: In such an embodiment, "m" is 0, "n" is 12, which represents a fatty acid moiety containing a myristate moiety, and R 1 is hydrogen. This embodiment is similar to trilaciclib, a CDK4 / 6 inhibitor currently in Phase 2 clinical trials for use in reducing side effects associated with chemotherapy. However, formula [2] includes a myristate moiety on the pyridinylpiperazine. While R in formula 2 is H, it will be understood that it can be C-C alkyl, substituted C-C alkyl such as haloalkyl, C-C cycloalkyl, substituted C-C cycloalkyl, aryl, substituted aryl, heteroaryl, and substituted heteroaryl, as described herein.

[0055] [ka]

[0056] Embodiments of the present approach, including those having the structures shown in Formula [2] above and Formula [3] below, include what the present disclosure refers to as pyridinylpiperazine-substituted fatty acids. In particular, the fatty acid moiety at this position in the structure significantly improves the cellular uptake of the compound and greatly enhances its inhibition of cancer stem cell proliferation, among other beneficial effects. As a result, compounds of the present approach inhibit the in vitro growth of lung cancer cell lines. These compounds may be useful as chemopreventive agents due to their ability to inhibit cell cycle progression in normal, non-transformed cells, as well as for treating cancer, reducing cancer resistance to treatment, preventing metastatic disease, preventing tumor recurrence, preventing at least one of radiotherapy resistance, chemotherapy resistance, and hormone therapy resistance, and / or preventing or reducing the proliferation of at least one of cancer cells, cancer stem cells, and circulating tumor cells.

[0057] [ka]

[0058] A second exemplary embodiment is shown above as equation [3]. R 1 is hydrogen, m is 2, and n is 14. As a result, this embodiment has a 14-carbon saturated fatty acid (i.e., palmitate) moiety. The compounds shown in formulas [2] and [3] exhibit significantly improved inhibition of MCF7 cells in a tumor mass assay compared to trilaciclib. It will be understood that similar results are expected with other fatty acid moieties having only 11, preferably at least 14, and as many as 22 carbons.

[0059] The present method describes a pharmaceutical composition comprising a therapeutically effective amount of a first or second compound, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent, or excipient thereof. The compound according to the present method can be used as an anti-cancer therapeutic agent. A pharmaceutically effective amount of the compound in a pharmaceutically acceptable carrier can be administered to a subject by means known in the art. In some embodiments, the compound according to the present method can be used in combination with other cancer therapies, such as, but not limited to, chemotherapeutic agents, mitochondrial biogenesis inhibitors (e.g., mitoribosin, mitochetocin, reprosin, e.g., antimitocin), radiation therapy, phototherapy, and thermal restriction.

[0060] Selective inhibition of CDK4 / 6 also indicates that the compounds described herein can be used to reduce or eliminate drug and / or treatment resistance in cancer. Because of their inhibitory activity against CDKs and other kinases, the compounds of this method are also useful research tools for investigating the mechanisms of action of these kinases and can be used both in vitro and in vivo.

[0061] The methods of treatment described herein are preferably carried out by administering to a subject in need of treatment a therapeutically effective amount of either the first or second compound, which are readily synthesized, can be administered by a variety of routes, including orally and parenterally, and have little or no toxicity.

[0062] Compounds prepared by this method can be synthesized from commercially available trilaciclib. Alternatively, synthetic options are publicly available, such as the synthetic scheme disclosed in U.S. Patent No. 8,598,197, the entire contents of which are incorporated herein by reference. Starting with trilaciclib, methylpiperazine can be demethylated using methods known in the art. After demethylation, myristoylation can be used to form the compound.

[0063] As another example, the following synthetic method can be used in embodiments having a myristate moiety: Myristic acid can be converted to myristate chloride and reacted with 2-methyl-2-propanyl 1-piperazinecarboxylate (shown below as 1-BOC-piperazine) in the presence of 4-methylmorpholine (NMM) and dichloromethane (DCM) as shown below.

[0064] [ka]

[0065] The intermediate product can be reacted with HCl and dioxane to form 1-(1-piperazinyl)-1-tetradecanone. The process continues as shown below. It will be understood that DiPEA is Hunig's base (N,N-diisopropylethylamine), DMA is dimethylacetamide, and THF is tetrahydrofuran. It will also be understood that the fatty acid moiety can be modified in the first step above with a desired alkyl.

[0066] [ka]

[0067] The terminology used in the description of embodiments of the present technique is merely for the purpose of describing particular embodiments and is not intended to be limiting. As used in the specification and claims, the singular forms "a," "an," and "the" are intended to include the plural forms as well, unless the context clearly dictates otherwise. The present technique encompasses numerous alternatives, modifications, and equivalents, as will be apparent from a consideration of the following detailed description.

[0068] While terms such as "first," "second," "third," "a)," "b)," and "c)" may be used herein to describe various elements of the present method, it will be understood that the claims should not be limited by these terms. These terms are used only to distinguish one element of the present method from another. Thus, a first element discussed below could be referred to as an aspect of an element and, similarly, as a third element, without departing from the teachings of the present method. Thus, terms such as "first," "second," "third," "a)," "b)," and "c)" are not necessarily intended to convey an order or other hierarchy of the associated elements, but are used for identification purposes only. The order of operations (or steps) is not limited to the order set forth in the claims.

[0069] Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by those skilled in the art. Terms defined in commonly used dictionaries should be interpreted as having a meaning consistent with the meaning in the context of this application and the prior art, and it will be further understood that they should not be interpreted in an idealized or overly formal sense unless expressly defined. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In the event of a conflict in terminology, the present specification controls.

[0070] Also, as used herein, "and / or" refers to and includes any and all possible combinations of one or more of the associated listed items, and when interpreted as an alternative ("or") refers to and includes the absence of combinations.

[0071] Unless the context dictates otherwise, it is specifically intended that the various features of the present approach described herein can be used in any combination. Furthermore, the present approach also contemplates that in some embodiments, any feature or combination of features described with respect to exemplary embodiments may be eliminated or omitted.

[0072] As used herein, the transitional phrase "consisting essentially of" (and grammatical variations thereof) should be interpreted as including the materials or steps recited in the claim "and which do not materially affect the basic and novel characteristics." Thus, as used herein, the term "consisting essentially of" should not be interpreted as equivalent to "comprise."

[0073] As used herein, when referring to a measurable value, such as an amount or concentration, the term "about" is meant to encompass a variation of ±20%, ±10%, ±5%, ±1%, ±0.5%, or ±0.1% of the particular amount. Ranges recited herein for measurable values ​​may include any other ranges and / or individual values ​​thereof.

[0074] While particular embodiments of the present approach have thus been described, it should be understood that the appended claims are not limited to the specific details set forth in the above specification, as many obvious variations thereof are possible without departing from the spirit or scope of the invention as claimed below.

Claims

1. General formula: 【Chemistry 1】 A compound comprising In the formula, "m" is an integer from 0 to 4, "n" is an integer from 12 to 22, and R １ is selected from the group consisting of hydrogen, C1-C8 alkyl, substituted C1-C8 alkyl, C3-C8 cycloalkyl, substituted C3-C8 cycloalkyl, aryl, substituted aryl, heteroaryl, and substituted heteroaryl.

2. 2. The compound of claim 1, wherein "m" is an integer from 0 to 2 and "n" is an integer from 14 to 20.

3. R １ is one of H, C1-C8 alkyl, and substituted C1-C8 alkyl.

4. m is 0, n is 12, and R １ The compound of claim 1 , wherein is hydrogen.

5. 10. A pharmaceutical composition comprising a compound according to any one of claims 1 to 4 and a pharmaceutically acceptable carrier.

6. A pharmaceutical composition for treating cancer, comprising a compound according to any one of claims 1 to 4 and a pharmaceutically acceptable carrier.

7. A pharmaceutical composition for reducing cancer treatment resistance, comprising a compound according to any one of claims 1 to 4 and a pharmaceutically acceptable carrier.

8. A pharmaceutical composition for treating or preventing metastatic disease, comprising a compound according to any one of claims 1 to 4 and a pharmaceutically acceptable carrier.

9. A pharmaceutical composition for treating or preventing tumor recurrence, comprising a compound according to any one of claims 1 to 4 and a pharmaceutically acceptable carrier.

10. A pharmaceutical composition for treating or preventing at least one of radiotherapy resistance, chemotherapy resistance, and hormone therapy resistance, comprising a compound described in any one of claims 1 to 4 and a pharmaceutically acceptable carrier.

11. A pharmaceutical composition for preventing or reducing the proliferation of at least one of cancer cells, cancer stem cells and circulating tumor cells, comprising a compound described in any one of claims 1 to 4 and a pharmaceutically acceptable carrier.

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