Use of isoquinoline compounds in tumor treatment

Abstract

The present invention relates to the use of isoquinoline compounds in tumor treatment. Specifically, the present invention provides the use of a compound of Formula I, or an optical isomer or racemate thereof, or a solvate thereof, or a pharmaceutically acceptable salt thereof, for preparing a composition or formulation, wherein the composition or formulation is used for the prevention and / or treatment of tumors. The compound of the present invention has significantly superior therapeutic effects against tumors with low or no expression of the NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of nucleotide sites in the NNMT gene, and / or hypermethylation of DNA CpG sites in the NNMT gene region.

Description

[Technical field]

[0001] The present invention relates to the technical field of medicine, in particular to the use of isoquinoline compounds in tumor therapy. [Background technology]

[0002] Tumors, as a common disease that seriously endangers the health of mankind, have also brought about a constant upward trend in the mortality rate of malignant tumors. Due to the heterogeneity of tumors and the individual differences of patients, if the same treatment method or the same drug is simply used according to the origin and pathological characteristics of the tumor, problems caused by inappropriate treatment are likely to occur, and the important treatment time and opportunity of the patient will be delayed. Therefore, it seems that there is a great need to adopt personalized treatment for various conditions of patients. With the development of biological technology, tumor treatment has also entered the era of precision treatment, and changes in the expression of tumor-related genes have been discovered one after another, and the transformation of related genes plays an important role in the development of malignant tumors. The discovery and use of such biomarkers, such as upregulating certain functions of cells and promoting the immortality of cancer cells, can provide precise guidance for the use of related drugs, enable personalized tumor treatment, achieve targeted dosing, and greatly improve the therapeutic effect.

[0003] Therefore, there is an urgent need in this field to develop drugs that can precisely treat tumors. Summary of the Invention [Problem to be solved by the invention]

[0004] The present invention aims to provide a marker for determining whether the compound of the present invention is suitable for the prevention and / or treatment of tumor patients based on the expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of the nucleotide site of the NNMT gene, and / or the methylation level of the DNA CpG site in the NNMT gene region, so as to perform precise tumor treatment. The compound of the present invention has a significantly superior therapeutic effect on tumors with low or no expression of the NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of the nucleotide site of the NNMT gene, and / or hypermethylation of the DNA CpG site in the NNMT gene region. [Means for solving the problem]

[0005] A first aspect of the present invention relates to the use of a compound of formula I, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, comprising preparing a composition or formulation, and wherein said composition or said formulation is used for the prevention and / or treatment of tumors. [ka]

[0006] Here, R1, R2, R3, R4, R 10 , R 11 , R 12 and R 13 each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C12 alkyl group, a substituted or unsubstituted C3-C12 cycloalkyl group, a substituted or unsubstituted C1-C12 alkoxyl group, a substituted or unsubstituted C1-C12 alkylthiol group, a substituted or unsubstituted 3-12 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-12 membered heteroaryl group; or R1 and R2, R2 and R3, R3 and R4, R 10 and R 11 , R 11 and R 12 , and R12 and R 13 each independently form a substituted or unsubstituted C3-C12 cycloalkyl ring, a substituted or unsubstituted 3-12 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-12 membered heteroaryl ring; R5, R6, R7, R8, R9 and R 14 each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C12 alkyl group, a substituted or unsubstituted C3-C12 cycloalkyl group, a substituted or unsubstituted C1-C12 alkoxyl group, a substituted or unsubstituted C1-C12 alkylthiol group, a substituted or unsubstituted 3-12 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-12 membered heteroaryl group; Here, the optional "substitution" refers to one or more (preferably one, two, three or four) hydrogen atoms on the atomic group being replaced with a C1-C8 alkyl group, a C3-C8 cycloalkyl group, a C2-C4 alkenyl group, a C2-C4 alkynyl group, a C1-C8 halogenated alkyl group, a C3-C8 halogenated cycloalkyl group, a halogen atom, a nitro group, -CN, a carbonyl group (=O), a cyano group, a hydroxyl group, a mercapto group, an amino group, a C1-C4 carboxyl group, a C2 -C8 ester group, C2-C4 acylamino group, C1-C8 alkoxyl group, C1-C8 alkylthiol group, C3-C8 cycloalkoxyl group, C3-C8 cycloalkylthiol group, C1-C8 halogenated alkoxyl group, C1-C8 halogenated alkylthiol group, C6-C12 aryl group, 5-10 membered heteroaryl group, 5-10 membered heterocycloalkyl group and pyrrolidine-2,5-diketone group; The heterocyclic rings of the heterocycloalkyl group, heteroaryl group, heterocycloalkyl ring and heteroaryl ring each independently have 1 to 4 (preferably 1, 2, 3 or 4) heteroatoms selected from N, O and S.

[0007] In another preferred embodiment, the cycloalkyl ring has 1, 2 or 3 C=C cyclic double bonds.

[0008] In another preferred embodiment, the heterocycloalkyl ring has 1, 2 or 3 C=C cyclic double bonds.

[0009] In another preferred example, the "substitution" means that one or more (preferably one, two, three or four) hydrogen atoms on the atomic group are replaced with a C1-C6 alkyl group, a C3-C8 cycloalkyl group, a C2-C4 alkenyl group, a C2-C4 alkynyl group, a C1-C6 halogenated alkyl group, a C3-C8 halogenated cycloalkyl group, a halogen atom, a nitro group, -CN, a carbonyl group (=O), a cyano group, a hydroxyl group, a mercapto group, an amino group, a C1-C4 carboxyl group, a C2 - refers to being substituted by a substituent selected from a C6 ester group, a C2-C4 acylamino group, a C1-C6 alkoxyl group, a C1-C6 alkylthiol group, a C3-C6 cycloalkoxyl group, a C3-C6 cycloalkylthiol group, a C1-C6 halogenated alkoxyl group, a C1-C6 halogenated alkylthiol group, a C6-C12 aryl group, a 5-10 membered heteroaryl group, a 5-10 membered heterocycloalkyl group, and a pyrrolidine-2,5-diketone group.

[0010] In another preferred example, the "substitution" means that one or more (preferably one, two, three or four) hydrogen atoms on the atomic group are replaced with a C1-C4 alkyl group, a C3-C8 cycloalkyl group, a C2-C4 alkenyl group, a C2-C4 alkynyl group, a C1-C4 halogenated alkyl group, a C3-C8 halogenated cycloalkyl group, a halogen atom, a nitro group, -CN, a carbonyl group (=O), a cyano group, a hydroxyl group, a mercapto group, an amino group, a C1-C4 carboxyl group, a C2 - refers to being substituted by a substituent selected from a C6 ester group, a C2-C4 acylamino group, a C1-C4 alkoxyl group, a C1-C4 alkylthiol group, a C3-C6 cycloalkoxyl group, a C3-C6 cycloalkylthiol group, a C1-C4 halogenated alkoxyl group, a C1-C4 halogenated alkylthiol group, a C6-C12 aryl group, a 5-10 membered heteroaryl group, a 5-10 membered heterocycloalkyl group, and a pyrrolidine-2,5-diketone group.

[0011] In another preferred example, the "substituted" refers to one or more (preferably one, two, three or four) hydrogen atoms on the atomic group being replaced by a substituent selected from a C1-C4 alkyl group, a C2-C4 alkenyl group, a C2-C4 alkynyl group, a halogen atom, a C1-C4 alkoxyl group, a C1-C4 carboxyl group and a C2-C6 ester group.

[0012] In another preferred example, the heterocyclic ring of the heterocycloalkyl group, heteroaryl group, heterocycloalkyl ring, and heteroaryl ring each independently has 1 to 4 (preferably 1, 2, 3, or 4) heteroatoms selected from N, O, and S.

[0013] In another preferred embodiment, R1 and R2, R2 and R3, R3 and R4, R 10 and R 11 , R 11 and R 12 , and R 12 and R 13each independently form a substituted or unsubstituted C3-C12 cycloalkyl ring, a substituted or unsubstituted 3-12 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-12 membered heteroaryl ring.

[0014] In another preferred embodiment, R1 and R2 are joined together to form a substituted or unsubstituted C3-C12 cycloalkyl ring, a substituted or unsubstituted 3-12 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-12 membered heteroaryl ring.

[0015] In another preferred embodiment, R2 and R3 together form a substituted or unsubstituted C3-C12 cycloalkyl ring, a substituted or unsubstituted 3-12 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-12 membered heteroaryl ring.

[0016] In another preferred embodiment, R3 and R4 are joined together to form a substituted or unsubstituted C3-C12 cycloalkyl ring, a substituted or unsubstituted 3-12 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-12 membered heteroaryl ring.

[0017] Another favorable example is R 10 and R 11 together form a substituted or unsubstituted C3-C12 cycloalkyl ring, a substituted or unsubstituted 3-12 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-12 membered heteroaryl ring.

[0018] Another favorable example is R 11 and R 12 together form a substituted or unsubstituted C3-C12 cycloalkyl ring, a substituted or unsubstituted 3-12 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-12 membered heteroaryl ring.

[0019] Another favorable example is R 12and R 13 together form a substituted or unsubstituted C3-C12 cycloalkyl ring, a substituted or unsubstituted 3-12 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-12 membered heteroaryl ring.

[0020] In another preferred embodiment, R1, R2, R3, R4, R 10 , R 11 , R 12 and R 13 each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C8 alkyl group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C10 alkoxyl group, a substituted or unsubstituted C1-C10 alkylthiol group, a substituted or unsubstituted 3-10 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-10 membered heteroaryl group; or R1 and R2, R2 and R3, R3 and R4, R 10 and R 11 , R 11 and R 12 , and R 12 and R 13 each independently form a substituted or unsubstituted C3-C8 cycloalkyl ring, a substituted or unsubstituted 3-10 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-10 membered heteroaryl ring.

[0021] In another preferred embodiment, R1, R2, R3, R4, R 10 , R 11 , R 12 and R 13each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C8 alkyl group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C8 alkoxyl group, a substituted or unsubstituted C1-C8 alkylthiol group, a substituted or unsubstituted 3-10 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-10 membered heteroaryl group; or R1 and R2, R2 and R3, R3 and R4, R 10 and R 11 , R 11 and R 12 , and R 12 and R 13 each independently form a substituted or unsubstituted C3-C8 cycloalkyl ring, a substituted or unsubstituted 3-10 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-10 membered heteroaryl ring.

[0022] In another preferred embodiment, R1, R2, R3, R4, R 10 , R 11 , R 12 and R 13 each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C6 alkyl group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C6 alkoxyl group, a substituted or unsubstituted C1-C6 alkylthiol group, a substituted or unsubstituted 3-10 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-10 membered heteroaryl group; or R1 and R2, R2 and R3, R3 and R4, R 10 and R 11 , R 11 and R 12 , and R 12 and R 13each independently form a substituted or unsubstituted C3-C8 cycloalkyl ring, a substituted or unsubstituted 3-10 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-10 membered heteroaryl ring.

[0023] In another preferred embodiment, R1, R2, R3, R4, R 10 , R 11 , R 12 and R 13 each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group; or R1 and R2, R2 and R3, R3 and R4, R 10 and R 11 , R 11 and R 12 , and R 12 and R 13 each independently form a substituted or unsubstituted C3-C6 cycloalkyl ring, a substituted or unsubstituted 3-8 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-8 membered heteroaryl ring.

[0024] In another preferred embodiment, R1, R2, R3, R4, R 10 , R 11 , R 12 and R 13each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group; or R1 and R2, R2 and R3, R3 and R4, R 10 and R 11 , R 11 and R 12 , and R 12 and R 13 each independently form a substituted or unsubstituted C3-C6 cycloalkyl ring, a substituted or unsubstituted 5-7 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-8 membered heteroaryl ring.

[0025] In another preferred embodiment, R1, R2, R3, R4, R 10 , R 11 , R 12 and R 13 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C6 alkyl group, a substituted or unsubstituted C1-C6 alkoxyl group, or a substituted or unsubstituted C1-C6 alkylthiol group; or R1 and R2, R2 and R3, R3 and R4, R 10 and R 11 , R 11 and R 12 , and R 12 and R 13 each independently form a substituted or unsubstituted C3-C6 cycloalkyl ring, or a substituted or unsubstituted 5- to 7-membered heterocycloalkyl ring.

[0026] In another preferred embodiment, R1, R2, R3 and R4 each independently represent a hydrogen atom, a substituted or unsubstituted C1-C6 alkyl group, or a substituted or unsubstituted C1-C6 alkoxyl group; or R2 and R3, R 10 and R 11 and R 11and R 12 each independently form a substituted or unsubstituted C3-C6 cycloalkyl ring, or a substituted or unsubstituted 5-7 membered heterocycloalkyl ring, wherein the heterocycloalkyl ring has 1 to 3 oxygen atoms.

[0027] In another preferred embodiment, the heterocycloalkyl ring is a substituted or unsubstituted [1,3]dioxazole ring.

[0028] In another preferred embodiment, R1 represents a hydrogen atom.

[0029] In another preferred embodiment, R2 and R3 together form a substituted or unsubstituted 3-membered heterocycloalkyl ring, a substituted or unsubstituted 4-membered heterocycloalkyl ring, a substituted or unsubstituted 5-membered heterocycloalkyl ring, a substituted or unsubstituted 6-membered heterocycloalkyl ring, a substituted or unsubstituted 7-membered heterocycloalkyl ring, a substituted or unsubstituted 8-membered heterocycloalkyl ring, a substituted or unsubstituted 9-membered heterocycloalkyl ring, a substituted or unsubstituted 10-membered heterocycloalkyl ring, a substituted or unsubstituted 11-membered heterocycloalkyl ring, or a substituted or unsubstituted 12-membered heterocycloalkyl ring.

[0030] In another preferred embodiment, R2 and R3 together form a substituted or unsubstituted [1,3]dioxole ring.

[0031] In the present invention, the structural formula of the [1,3]dioxazole ring is: [ka]

[0032] In another preferred embodiment, R2 and R3 are each independently substituted or unsubstituted. [ka] Forming; Here A stands for O or S; W stands for O or S; R 15 and R 16 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group.

[0033] In another preferred embodiment, A is O or S.

[0034] In another preferred embodiment, W represents O or S.

[0035] In another preferred embodiment, R2 and R3 are each independently substituted or unsubstituted. [ka] where A is O or S; R 15 and R 16 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group.

[0036] In another preferred embodiment, R1 and R2, R2 and R3, R3 and R4, R 10 and R 11 , R 11 and R 12 , and R 12 and R 13 are each independently a 5-7 membered heterocycloalkyl ring, preferably [ka] Form.

[0037] In another preferred embodiment, R2 and R3 are each independently substituted or unsubstituted. [ka] Form.

[0038] In another preferred embodiment, R4 represents a hydrogen atom.

[0039] In another preferred embodiment, R5, R6, R7, R8, R9 and R 14 each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C8 alkyl group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C8 alkoxyl group, a substituted or unsubstituted C1-C8 alkylthiol group, a substituted or unsubstituted 3-10 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-10 membered heteroaryl group.

[0040] In another preferred embodiment, R5, R6, R7, R8, R9 and R 14 each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C6 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C6 alkoxyl group, a substituted or unsubstituted C1-C6 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group.

[0041] In another preferred embodiment, R5, R6, R7, R8, R9 and R 14each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group.

[0042] In another preferred embodiment, R5, R6, R7, R8, R9 and R 14 each independently represents a hydrogen atom, a methyl group, an ethyl group, a propyl group, or a butyl group.

[0043] Another favorable example is R 10 , R 11 and R 12 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C6 alkoxyl group, or a substituted or unsubstituted C1-C6 alkylthiol group; or R 10 and R 11 and R 11 and R 12 each, independently of one another, form a substituted or unsubstituted 3-membered heterocycloalkyl ring, a substituted or unsubstituted 4-membered heterocycloalkyl ring, a substituted or unsubstituted 5-membered heterocycloalkyl ring, a substituted or unsubstituted 6-membered heterocycloalkyl ring, a substituted or unsubstituted 7-membered heterocycloalkyl ring, a substituted or unsubstituted 8-membered heterocycloalkyl ring, a substituted or unsubstituted 9-membered heterocycloalkyl ring, a substituted or unsubstituted 10-membered heterocycloalkyl ring, a substituted or unsubstituted 11-membered heterocycloalkyl ring, or a substituted or unsubstituted 12-membered heterocycloalkyl ring.

[0044] Another favorable example is R 10 , R 11 and R 12 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C4 alkoxyl group, or a substituted or unsubstituted C1-C4 alkylthiol group; or R 10 and R 11 and R11 and R 12 each, independently of one another, form a substituted or unsubstituted 3-membered heterocycloalkyl ring, a substituted or unsubstituted 4-membered heterocycloalkyl ring, a substituted or unsubstituted 5-membered heterocycloalkyl ring, a substituted or unsubstituted 6-membered heterocycloalkyl ring, a substituted or unsubstituted 7-membered heterocycloalkyl ring, a substituted or unsubstituted 8-membered heterocycloalkyl ring, a substituted or unsubstituted 9-membered heterocycloalkyl ring, a substituted or unsubstituted 10-membered heterocycloalkyl ring, a substituted or unsubstituted 11-membered heterocycloalkyl ring, or a substituted or unsubstituted 12-membered heterocycloalkyl ring.

[0045] In another preferred embodiment, the heterocycloalkyl ring is a substituted or unsubstituted [1,3]dioxazole ring.

[0046] Another favorable example is R 10 , R 11 and R 12 are each independently a hydrogen atom or R 17 -A- stands for; where A is O or S; R 17 represents a substituted or unsubstituted C1-C10 alkyl group, a C2-C4 alkenyl group-C1-C4 alkyl group-, a C2-C8 ester group-C1-C4 alkyl group-, a halogenated C1-C12 alkyl group-, a 5- to 7-membered heterocycloalkyl group-C1-C4 alkyl group-, a pyrrolidine-2,5-diketone group-C1-C4 alkyl group-, a cyano group-C1-C4 alkyl group-, a C1-C4 alkoxyl group-C2-C4 alkyl group-, a C2-C4 alkylthiol group-C1-C4 alkyl group-, or a 5- to 7-membered heteroaryl group-C1-C4 alkyl group-.

[0047] Another favorable example is R 17represents a substituted or unsubstituted C3-C10 alkyl group, a C2-C4 alkenyl group-C1-C4 alkyl group-, a C2-C8 ester group-C1-C4 alkyl group-, a halogenated C1-C12 alkyl group-, a 5-7-membered heterocycloalkyl group-C1-C4 alkyl group-, a pyrrolidine-2,5-diketone group-C1-C4 alkyl group-, a cyano group-C1-C4 alkyl group-, a C1-C4 alkoxyl group-C2-C4 alkyl group-, a C2-C4 alkylthiol group-C1-C4 alkyl group-, or a 5-7-membered heteroaryl group-C1-C4 alkyl group-.

[0048] Another favorable example is R 17 represents a substituted or unsubstituted C1-C6 alkyl group, a C2-C4 alkenyl group-C1-C4 alkyl group-, a C2-C8 ester group-C1-C4 alkyl group-, a halogenated C1-C12 alkyl group-, a 5- to 7-membered heterocycloalkyl group-C1-C4 alkyl group-, a pyrrolidine-2,5-diketone group-C1-C4 alkyl group-, a cyano group-C1-C4 alkyl group-, a C1-C4 alkoxyl group-C2-C4 alkyl group-, a C2-C4 alkylthiol group-C1-C4 alkyl group-, or a 5- to 7-membered heteroaryl group-C1-C4 alkyl group-.

[0049] Another favorable example is R 17 represents a substituted or unsubstituted C3-C6 alkyl group, a C2-C4 alkenyl group-C1-C4 alkyl group-, a C2-C8 ester group-C1-C4 alkyl group-, a halogenated C1-C12 alkyl group-, a 5-7-membered heterocycloalkyl group-C1-C4 alkyl group-, a pyrrolidine-2,5-diketone group-C1-C4 alkyl group-, a cyano group-C1-C4 alkyl group-, a C1-C4 alkoxyl group-C2-C4 alkyl group-, a C2-C4 alkylthiol group-C1-C4 alkyl group-, or a 5-7-membered heteroaryl group-C1-C4 alkyl group-.

[0050] Another favorable example is R 17 represents a substituted or unsubstituted C1-C6 alkyl group, a C2-C4 alkenyl group -C1-C2 alkyl group-, or a C2-C8 ester group -C1-C2 alkyl group-.

[0051] Another favorable example is R 17 represents a substituted or unsubstituted C1-C4 alkyl group, a C2-C4 alkenyl group -C1-C2 alkyl group-, or a C2-C8 ester group -C1-C2 alkyl group-.

[0052] Another favorable example is R 17 represents a substituted or unsubstituted C1-C4 alkyl group, a C2-C4 alkenyl group -C1-C2 alkyl group-, or a C3-C7 ester group -C1-C2 alkyl group-.

[0053] Another favorable example is R 17 represents a substituted or unsubstituted C3-C6 alkyl group, a C2-C4 alkenyl group -C1-C2 alkyl group-, or a C2-C8 ester group -C1-C2 alkyl group-.

[0054] Another favorable example is R 17 represents a methyl group, an ethyl group, a propyl group, a butyl group, an amyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a vinyl group-methyl group, an amyl ester group-methyl group, a halogenated propyl group, a halogenated decyl group, a morpholinyl group-ethyl group, a pyrrolidine-2,5-diketone group-ethyl group, a cyano group-methyl group, a methoxy group-ethyl group, or a pyridine group-methyl group.

[0055] In another preferred example, the amyl ester group is -COOC(CH3)3.

[0056] In another preferred embodiment, the halogenation is monohalogenated, dihalogenated or trihalogenated.

[0057] In another preferred embodiment, the propyl group is an N-propyl group.

[0058] In another preferred embodiment, the decyl group is an N-decyl group.

[0059] In another preferred embodiment, the hexyl group is an N-hexyl group.

[0060] Another favorable example is R 10 , R 11 and R 12 each independently represents a hydrogen atom, a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a methylthio group, an ethylthio group, a propylthio group, or a butylthiol group.

[0061] Another favorable example is R 10 and R 11 , and R 11 and R 12 each independently form a substituted or unsubstituted [1,3]dioxazole ring.

[0062] Another favorable example is R 10 and R 11 are substituted or unsubstituted with each other. [ka] Here A stands for O or S; W stands for O or S; R 15 and R 16 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group.

[0063] Another favorable example is R 10 and R 11 together form a substituted or unsubstituted [1,3]dioxazole ring.

[0064] Another favorable example is R 10 and R 11 are substituted or unsubstituted with each other. [ka] where A is O or S; R 15 and R 16 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group.

[0065] Another favorable example is R 10 and R 11 are substituted or unsubstituted with each other. [ka] Form.

[0066] Another favorable example is R 11 and R 12 together form a substituted or unsubstituted [1,3]dioxazole ring.

[0067] Another favorable example is R 11 and R 12 are substituted or unsubstituted with each other. [ka] Forming; Here A stands for O or S; W stands for O or S; R 15 and R 16 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group.

[0068] In another preferred embodiment, A is O or S.

[0069] In another preferred embodiment, W represents O or S.

[0070] Another favorable example is R 11 and R 12 are substituted or unsubstituted with each other. [ka] where A is O or S; R 15 and R 16 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group.

[0071] Another favorable example is R 11 and R 12 are substituted or unsubstituted with each other. [ka] Form.

[0072] Another favorable example is R 13 represents a hydrogen atom, a substituted or unsubstituted C1-C6 alkoxyl group, or a substituted or unsubstituted C1-C6 alkylthiol group.

[0073] Another favorable example is R 13 represents a hydrogen atom.

[0074] Another favorable example is R 14 represents a hydrogen atom, a methyl group, an ethyl group, a propyl group, or a butyl group.

[0075] Another favorable example is R 14 represents a methyl group.

[0076] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula I-1: [ka] where A is O or S; R1, R4, R5, R6, R7, R8, R9, R 10 , R 11 , R 12 , R 13 and R 14 is defined as above.

[0077] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula I-2: [ka] where A is O or S; R1, R4, R5, R6, R7, R8, R9, R 10 , R 13 and R 14 is defined as above.

[0078] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula I-3: [ka] where A is O or S; R1, R4, R5, R6, R7, R8, R9, R 12 , R 13 and R 14 is defined as above.

[0079] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula I-4: [ka] where A is O or S; W stands for O or S; R1, R4, R5, R6, R7, R8, R9, R 10 , R11 , R 12 , R 13 and R 14 is defined as above.

[0080] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula I-5: [ka] where A is O or S; W stands for O or S; R1, R4, R5, R6, R7, R8, R9, R 10 , R 13 and R 14 is defined as above.

[0081] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula I-6: [ka] where A is O or S; W stands for O or S; R1, R4, R5, R6, R7, R8, R9, R 12 , R 13 and R 14 is defined as above.

[0082] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula: [ka]

[0083] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula: [ka] JPEG0007616583000021.jpg109147

[0084] In another preferred embodiment, the compounds of formula I include berberine and coptisine.

[0085] In another preferred embodiment, the berberine comprises berberine chloride or berberine sulfate.

[0086] In another preferred embodiment, the coptisine comprises coptisine chloride or coptisine sulfate.

[0087] In another preferred embodiment, the pharma- ceutically acceptable salt of the compound of formula I is a salt formed by the compound of formula I with an acid selected from hydrochloric acid, galactaric acid, D-glucuronic acid, hydrobromic acid, hydrofluoric acid, sulfuric acid, nitric acid, phosphoric acid, formic acid, acetic acid, trifluoroacetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tartaric acid, citric acid, picric acid, methanesulfonic acid, benzenesulfonic acid, benzenesulfonic acid, aspartic acid, and glutamic acid, or a combination thereof, preferably an acid selected from hydrochloric acid, hydrobromic acid, and sulfuric acid, or a combination thereof.

[0088] In another preferred embodiment, the tumor is of human origin.

[0089] In another preferred embodiment, the tumor is a human tumor.

[0090] In another preferred embodiment, the tumor comprises a tumor in which the NNMT gene is underexpressed or not expressed.

[0091] In another preferred embodiment, the tumor comprises a tumor in which DNA methyltransferase is highly expressed.

[0092] In another preferred embodiment, the DNA methyltransferase is selected from DNMT1, DNMT3a, DNMT3b, or a combination thereof.

[0093] In another preferred embodiment, the tumor comprises a tumor in which DNMT1 is highly expressed.

[0094] In another preferred embodiment, the tumor comprises a tumor in which DNMT3a is highly expressed.

[0095] In another preferred embodiment, the tumor comprises a tumor in which DNMT3b is highly expressed.

[0096] In another preferred embodiment, the tumor comprises a tumor in which UHRF1 is highly expressed.

[0097] In another preferred embodiment, the tumor comprises a tumor with hypermethylation of nucleotide sites in the NNMT gene and / or hypermethylation of DNA CpG sites in the NNMT gene region.

[0098] In another preferred embodiment, the tumor comprises a tumor in which the nucleotide site in the NNMT gene is hypermethylated.

[0099] In another preferred embodiment, the tumor comprises a tumor in which NNMT gene region DNA CpG sites are hypermethylated.

[0100] In another preferred embodiment, the NNMT gene is a human-derived NNMT gene.

[0101] In another preferred embodiment, the NNMT gene is a human NNMT gene.

[0102] In another preferred embodiment, a tumor in which the NNMT gene is under-expressed or not expressed refers to a tumor in which NNMT protein cannot be detected with an NNMT antibody in 1 μg of protein extracted from the tumor, and more preferably in 5 μg, 10 μg, 100 μg or 1000 μg of protein.

[0103] In another preferred example, a tumor in which the NNMT gene is under-expressed or not expressed refers to a tumor in which the expression level of the NNMT gene in tumor cells is lower than the expression level of the NNMT gene in the same cells or normal cells (e.g., cancerous bladder tissue cells).

[0104] In another preferred example, a tumor in which the NNMT gene is under-expressed or not expressed refers to a tumor in which the ratio (E1 / E0) between the expression level E1 of the NNMT gene in a tumor cell and the expression level E0 of the NNMT gene in the same cell or a normal cell (e.g., a cancerous bladder tissue cell) is <1.0.

[0105] In another preferred example, a tumor in which the NNMT gene is under-expressed or not expressed refers to a tumor in which the ratio (E1 / E0) between the expression level E1 of the NNMT gene in a certain cell (e.g., a tumor cell) and the expression level E0 of the NNMT gene in the same cell or a normal cell (e.g., a cancerous bladder tissue cell) is ≦1.0, preferably ≦0.7, and more preferably ≦0.6, ≦0.5, ≦0.4, ≦0.3, ≦0.2, ≦0.1, ≦0.05, ≦0.01, ≦0.005, ≦0.001, ≦0.0001, ≦0.00001, ≦0.000001 or ≦0.0000001.

[0106] In another preferred embodiment, the identical cells refer to cells in which the NNMT gene is normally expressed (analogous tumor cells).

[0107] In another preferred embodiment, said identical cells refer to similar cells, nevertheless, cells in which the NNMT gene is normally expressed.

[0108] In another preferred embodiment, the normal cells refer to normal tissue cells in which the NNMT gene is normally expressed (eg, cells derived from tumor cells, tumor-adjacent cells, or cancerous bladder tissue cells).

[0109] In another preferred embodiment, E0 is the expression level of the NNMT gene in cells in which the NNMT gene is normally expressed.

[0110] In another preferred embodiment, the cells in which the NNMT gene is normally expressed include cells that are insensitive to the compound of formula I, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof.

[0111] In another preferred embodiment, the tumor in which DNA methyltransferase is highly expressed refers to a tumor in which DNA methyltransferase can be detected with a DNA methyltransferase antibody in 20 μg of protein extracted from the tumor, more preferably in 5 μg, 1 μg, 0.2 μg, 0.1 μg or 0.05 μg of protein.

[0112] In another preferred embodiment, the tumor in which the DNA methyltransferase is highly expressed refers to a tumor in which the expression level of the DNA methyltransferase in tumor cells is greater than the expression level of the DNA methyltransferase in the same cells or normal cells (e.g., cancerous bladder tissue cells).

[0113] In another preferred embodiment, the tumor in which the DNA methyltransferase is highly expressed refers to a tumor in which the ratio (A1 / A0) between the expression level A1 of the DNA methyltransferase in tumor cells and the expression level A0 of the DNA methyltransferase in the same cells or normal cells (e.g., cancerous bladder tissue cells) is >1.0, preferably ≧1.2 or ≧1.5, and more preferably ≧2, ≧3, ≧5, ≧8, ≧10, ≧15, ≧20, ≧30 or ≧50.

[0114] In another preferred embodiment, the identical cells refer to cells in which DNA methyltransferase is normally expressed (analogous tumor cells).

[0115] In another preferred embodiment, said identical cell refers to a similar cell, but in which DNA methyltransferase is normally expressed.

[0116] In another preferred embodiment, the normal cells refer to normal tissue cells in which DNA methyltransferase is normally expressed (eg, cells derived from a tumor cell, cells adjacent to a tumor, or cancerous bladder tissue cells).

[0117] In another preferred embodiment, A0 is the expression level of DNA methyltransferase in cells in which DNA methyltransferase is normally expressed.

[0118] In another preferred embodiment, the cells in which the DNA methyltransferase is normally expressed include cells that are insensitive to isoquinoline compounds.

[0119] In another preferred embodiment, the tumor in which DNMT1 is highly expressed refers to a tumor in which DNMT1 protein can be detected with a DNMT1 antibody in 20 μg of protein extracted from the tumor, more preferably in 5 μg, 1 μg, 0.2 μg, 0.05 μg or 0.01 μg of protein.

[0120] In another preferred embodiment, the tumor in which DNMT1 is highly expressed refers to a tumor in which the expression level of DNMT1 in tumor cells is greater than the expression level of DNMT1 in the same cells or normal cells (e.g., cancerous bladder tissue cells).

[0121] In another preferred example, the tumor in which the DNMT1 is highly expressed refers to a tumor in which the ratio (B1 / B0) between the expression level B1 of DNMT1 in tumor cells and the expression level B0 of DNMT1 in the same cells or normal cells (e.g., cancerous bladder tissue cells) is >1.0, preferably ≧1.2 or ≧1.5, and more preferably ≧2, ≧3, ≧5, ≧8, ≧10, ≧15, ≧20, ≧30 or ≧50.

[0122] In another preferred embodiment, the same cells refer to cells in which DNMT1 is normally expressed (analogous tumor cells).

[0123] In another preferred embodiment, said identical cells refer to similar cells, nevertheless, cells in which DNMT1 is normally expressed.

[0124] In another preferred embodiment, the normal cells refer to normal tissue cells in which DNMT1 is normally expressed (eg, cells derived from a tumor cell, cells adjacent to a tumor, or cancerous bladder tissue cells).

[0125] In another preferred embodiment, B0 is the expression level of DNMT1 in cells in which DNMT1 is normally expressed.

[0126] In another preferred embodiment, the cells in which the DNMT1 is normally expressed include cells that are insensitive to isoquinoline compounds.

[0127] In another preferred embodiment, the tumor in which DNMT3a is highly expressed refers to a tumor in which DNMT3a protein can be detected with a DNMT3a antibody in 20 μg of protein extracted from the tumor, more preferably in 5 μg, 1 μg, 0.2 μg, 0.05 μg or 0.01 μg of protein.

[0128] In another preferred embodiment, the tumor with high expression of DNMT3a refers to a tumor in which the expression level of DNMT3a in tumor cells is greater than the expression level of DNMT3a in the same cells or normal cells (e.g., cancerous bladder tissue cells).

[0129] In another preferred example, the tumor in which the DNMT3a is highly expressed refers to a tumor in which the ratio (C1 / C0) between the expression level C1 of DNMT3a in tumor cells and the expression level C0 of DNMT3a in the same cells or normal cells (e.g., cancerous bladder tissue cells) is >1.0, preferably ≧1.2 or ≧1.5, and more preferably ≧2, ≧3, ≧5, ≧8, ≧10, ≧15, ≧20, ≧30 or ≧50.

[0130] In another preferred embodiment, the same cells refer to cells in which DNMT3a is normally expressed (analogous tumor cells).

[0131] In another preferred embodiment, said identical cells refer to similar cells, nevertheless, cells in which DNMT3a is normally expressed.

[0132] In another preferred embodiment, the normal cells refer to normal tissue cells in which DNMT3a is normally expressed (e.g., cells derived from a tumor cell, cells adjacent to a tumor, or cancerous bladder tissue cells).

[0133] In another preferred embodiment, C0 is the expression level of DNMT3a in cells in which DNMT3a is normally expressed.

[0134] In another preferred embodiment, the cells in which the DNMT3a is normally expressed include cells that are insensitive to isoquinoline compounds.

[0135] In another preferred embodiment, the tumor in which DNMT3b is highly expressed refers to a tumor in which DNMT3b protein can be detected with a DNMT3b antibody in 20 μg of protein extracted from the tumor, more preferably in 5 μg, 1 μg, 0.2 μg, 0.05 μg or 0.01 μg of protein.

[0136] In another preferred embodiment, the tumor in which DNMT3b is highly expressed refers to a tumor in which the expression level of DNMT3b in tumor cells is greater than the expression level of DNMT3b in the same cells or normal cells (e.g., cancerous bladder tissue cells).

[0137] In another preferred example, the tumor in which the DNMT3b is highly expressed refers to a tumor in which the ratio (D1 / D0) between the expression level D1 of DNMT3b in tumor cells and the expression level D0 of DNMT3b in the same cells or normal cells (e.g., cancerous bladder tissue cells) is >1.0, preferably ≧1.2 or ≧1.5, and more preferably ≧2, ≧3, ≧5, ≧8, ≧10, ≧15, ≧20, ≧30 or ≧50.

[0138] In another preferred embodiment, the same cells refer to cells in which DNMT3b is normally expressed (analogous tumor cells).

[0139] In another preferred embodiment, said identical cell refers to a similar cell, yet in which DNMT3b is normally expressed.

[0140] In another preferred embodiment, the normal cells refer to normal tissue cells in which DNMT3b is normally expressed (eg, cells derived from a tumor cell, cells adjacent to a tumor, or cancerous bladder tissue cells).

[0141] In another preferred embodiment, D0 is the expression level of DNMT3b in cells in which DNMT3b is normally expressed.

[0142] In another preferred embodiment, the cells in which the DNMT3b is normally expressed include cells that are insensitive to isoquinoline compounds.

[0143] In another preferred embodiment, the tumor in which UHRF1 is highly expressed refers to a tumor in which UHRF1 protein can be detected with a UHRF1 antibody in 20 μg of protein extracted from the tumor, more preferably in 5 μg, 1 μg, 0.2 μg, 0.05 μg or 0.01 μg of protein.

[0144] In another preferred example, the tumor in which UHRF1 is highly expressed refers to a tumor in which the expression level of UHRF1 in tumor cells is greater than the expression level of UHRF1 in the same cells or normal cells (eg, cancerous bladder tissue cells).

[0145] In another preferred example, the tumor in which UHRF1 is highly expressed refers to a tumor in which the ratio (F1 / F0) between the expression level F1 of UHRF1 in tumor cells and the expression level F0 of UHRF1 in the same cells or normal cells (e.g., cancerous bladder tissue cells) is >1.0, preferably ≧1.2 or ≧1.5, and more preferably ≧2, ≧3, ≧5, ≧8, ≧10, ≧15, ≧20, ≧30 or ≧50.

[0146] In another preferred embodiment, the same cells refer to cells in which UHRF1 is normally expressed (analogous tumor cells).

[0147] In another preferred embodiment, said identical cell refers to a similar cell, yet one in which UHRF1 is normally expressed.

[0148] In another preferred embodiment, the normal cells refer to normal tissue cells in which UHRF1 is normally expressed (eg, cells derived from a tumor cell, cells adjacent to a tumor, or cancerous bladder tissue cells).

[0149] In another preferred embodiment, F0 is the expression level of UHRF1 in cells in which UHRF1 is normally expressed.

[0150] In another preferred embodiment, the cells in which UHRF1 is normally expressed include cells that are insensitive to isoquinoline compounds.

[0151] In another preferred embodiment, a tumor in which the nucleotide site of the NNMT gene is hypermethylated refers to a tumor in which the methylation level of the nucleotide site of the NNMT gene in a certain cell (e.g., a tumor cell) is greater than the methylation level of the nucleotide site of the NNMT gene in the same cell or in a normal cell (e.g., a cancerous bladder tissue cell).

[0152] In another preferred embodiment, a tumor in which the nucleotide site of the NNMT gene is hypermethylated refers to a tumor in which the ratio (L1 / L0) between the methylation level L1 of the nucleotide site of the NNMT gene in a certain cell (e.g., a tumor cell) and the methylation level L0 of the nucleotide site of the NNMT gene in the same cell or a normal cell (e.g., a cancerous bladder tissue cell) is >1.0, preferably ≧1.2 or ≧1.5, and more preferably ≧2, ≧3, ≧5, ≧8, ≧10, ≧15, ≧20, ≧30 or ≧50.

[0153] In another preferred embodiment, a tumor in which the nucleotide site of the NNMT gene is hypermethylated refers to a tumor in which the methylation level of the nucleotide site of the NNMT gene in a certain cell (e.g., a tumor cell) is ≧1%, preferably ≧3%, ≧5%, ≧10%, ≧15% or ≧20%, and more preferably ≧25%, ≧30%, ≧40% or ≧50%.

[0154] In another preferred embodiment, said identical cells refer to cells in which the nucleotide site of the NNMT gene is normally methylated (analogous tumor cells).

[0155] In another preferred embodiment, said identical cell refers to a similar cell, but in which the nucleotide site of the NNMT gene is normally methylated.

[0156] In another preferred embodiment, the normal cells refer to normal tissue cells (eg, cells derived from tumor cells, tumor-adjacent cells, or cancerous bladder tissue cells) in which the nucleotide site of the NNMT gene is normally methylated.

[0157] In another preferred embodiment, cells in which the nucleotide site of the NNMT gene is normally methylated include cells that are insensitive to a compound of formula I, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof.

[0158] In another preferred example, a tumor in which the nucleotide site of the NNMT gene is hypermethylated refers to a tumor in which the methylation level (M%) of the nucleotide site of the NNMT gene in a certain cell (e.g., a tumor cell) is ≧3% and less than M1%, where M1 is any positive integer between 3 and 100.

[0159] In another preferred embodiment, M1 is 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 80, 85, 90, 95 or 100.

[0160] In another preferred embodiment, the methylation level of said nucleotide site of the NNMT gene refers to the ratio between the number of methylated nucleotides in the NNMT gene region and the number of all nucleotides in the NNMT gene region.

[0161] In another preferred embodiment, the methylation level of the nucleotide site of the NNMT gene comprises the methylation level of the nucleotide site of the NNMT gene promoter region.

[0162] In another preferred embodiment, the nucleotide sequence of the NNMT gene promoter region is shown in SEQ ID NO:1.

[0163] In another preferred embodiment, the methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide site within the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site.

[0164] In another preferred example, the region from 1050 bp before the transcription initiation site of the NNMT gene to 499 bp after the transcription initiation site corresponds to positions 951 to 2500 of the nucleotide sequence shown in SEQ ID NO:1.

[0165] In another preferred embodiment, the methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide site within the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site.

[0166] In another preferred example, the region from 1050 bp before the transcription initiation site of the NNMT gene to 193 bp before the transcription initiation site corresponds to positions 951 to 1808 of the nucleotide sequence shown in SEQ ID NO:1.

[0167] In another preferred embodiment, the methylation level of the nucleotide site of the NNMT gene comprises the methylation level of the nucleotide site within the region from 840 bp before the transcription start site to 469 bp before the transcription start site of the NNMT gene.

[0168] In another preferred example, the region from 840 bp before the transcription initiation site of the NNMT gene to 469 bp before the transcription initiation site corresponds to positions 1161 to 1532 of the nucleotide sequence shown in SEQ ID NO:1.

[0169] In another preferred embodiment, the methylation level of the nucleotide site of the NNMT gene includes the methylation level of a nucleotide site within a region between any two of positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050, and 114166066 on human chromosome 11 (including these two positions themselves).

[0170] In another preferred embodiment, the methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide at one or more (e.g., 2, 3, 4, 5, 6 or 7) sites among positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050 and 114166066 of human chromosome 11.

[0171] In another preferred embodiment, the methylation level of the nucleotide site of the NNMT gene comprises the methylation level of a nucleotide at a site selected from position 114165695 of human chromosome 11, position 114165730 of human chromosome 11, position 114165769 of human chromosome 11, position 114165804 of human chromosome 11, position 114165938 of human chromosome 11, position 114166050 of human chromosome 11, position 114166066 of human chromosome 11, or a combination thereof.

[0172] In another preferred embodiment, the methylation level of the nucleotide site of the NNMT gene includes the methylation level of a nucleotide site within a region between any two of positions 1161, 1196, 1235, 1270, 1404, 1516, and 1532 of the nucleotide sequence of SEQ ID NO:1 (including these two positions themselves).

[0173] In another preferred embodiment, the methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide at one or more (e.g., 2, 3, 4, 5, 6 or 7) of positions 1161, 1196, 1235, 1270, 1404, 1516 and 1532 of the nucleotide sequence of SEQ ID NO:1.

[0174] In another preferred embodiment, the methylation level of the NNMT gene region DNA CpG site comprises the methylation level of the nucleotides at the sites selected from the sites 1161, 1196, 1235, 1270, 1404, 1516, 1532 or combinations thereof of the nucleotide sequence of SEQ ID NO:1.

[0175] In another preferred embodiment, a tumor in which the DNA CpG site in the NNMT gene region is hypermethylated refers to a tumor in which the methylation level of the DNA CpG site in the NNMT gene region in a certain cell (e.g., a tumor cell) is greater than the methylation level of the DNA CpG site in the NNMT gene region in the same cell or in a normal cell (e.g., a cancerous bladder tissue cell).

[0176] In another preferred embodiment, the tumor in which the DNA CpG site in the NNMT gene region is hypermethylated refers to a tumor in which the ratio (W1 / W0) between the methylation level W1 of the DNA CpG site in the NNMT gene region of a certain cell (e.g., a tumor cell) and the methylation level W0 of the DNA CpG site in the NNMT gene region of the same cell or a normal cell (e.g., a cancerous bladder tissue cell) is >1.0, preferably ≧1.2 or ≧1.5, and more preferably ≧2, ≧3, ≧5, ≧8, ≧10, ≧15, ≧20, ≧30 or ≧50.

[0177] In another preferred embodiment, the tumor in which the DNA CpG site in the NNMT gene region is hypermethylated refers to a tumor in which the methylation level of the DNA CpG site in the NNMT gene region of a certain cell (e.g., tumor cell) is ≧1%, preferably ≧3%, ≧5%, ≧10%, ≧15% or ≧20%, and more preferably ≧25%, ≧30%, ≧40% or ≧50%.

[0178] In another preferred embodiment, the identical cells refer to cells in which the NNMT gene region DNA CpG sites are normally methylated (similar tumor cells).

[0179] In another preferred embodiment, said identical cells refer to similar cells, nevertheless, cells in which the NNMT gene region DNA CpG sites are normally methylated.

[0180] In another preferred embodiment, the normal cells refer to normal tissue cells (eg, cells derived from tumor cells, tumor-adjacent cells, or cancerous bladder tissue cells) in which the DNA CpG sites in the NNMT gene region are normally methylated.

[0181] In another preferred embodiment, cells in which the NNMT gene region DNA CpG sites are normally methylated include cells that are insensitive to a compound of formula I, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof.

[0182] In another preferred example, the tumor in which the DNA CpG site in the NNMT gene region is hypermethylated refers to a tumor in which the methylation level (M%) of the DNA CpG site in the NNMT gene region of a certain cell (e.g., a tumor cell) is ≧3% and less than M2%, where M2 is any positive integer between 3 and 100.

[0183] In another preferred embodiment, M2 is 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 80, 85, 90, 95 or 100.

[0184] In another preferred embodiment, the methylation level of the CpG site refers to the ratio between the number of methylated CpG nucleotides in a gene region and the number of all nucleotides in the gene region.

[0185] In another preferred embodiment, the methylation level of the DNA CpG site of the NNMT gene region refers to the ratio between the number of methylated CpG nucleotides in the NNMT gene region and the number of all nucleotides in the NNMT gene region.

[0186] In another preferred embodiment, the methylation level of the CpG site refers to the ratio between the number of methylated CpG nucleotides in a gene region and the number of all CpG nucleotides in the gene region.

[0187] In another preferred embodiment, the methylation level of said NNMT gene region DNA CpG site refers to the ratio between the number of methylated CpG nucleotides in the NNMT gene region and the number of all CpG nucleotides in the NNMT gene region.

[0188] In another preferred embodiment, the methylation level of DNA CpG sites refers to the ratio between the number of methylated CpG sites in a region of DNA and the number of all CpG sites in the region of DNA.

[0189] In another preferred embodiment, the methylation level of the DNA CpG site refers to the ratio between the number of methylated CpG nucleotides in a region of DNA and the number of all nucleotides in the region of DNA.

[0190] In another preferred embodiment, the methylation level of the DNA CpG site refers to the ratio between the number of methylated CpG nucleotides in a region of DNA and the number of all CpG nucleotides in the region of DNA.

[0191] In another preferred embodiment, the methylation level of the NNMT gene region DNA CpG sites refers to the ratio between the number of methylated CpG sites in the NNMT gene region DNA and the number of all CpG sites in the NNMT gene region DNA.

[0192] In another preferred embodiment, the methylation level of the NNMT gene region DNA CpG site refers to the ratio between the number of methylated CpG nucleotides in the NNMT gene region DNA and the number of all CpG nucleotides in the NNMT gene region DNA.

[0193] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region comprises the methylation level of DNA CpG sites in the NNMT gene promoter region.

[0194] In another preferred embodiment, the nucleotide sequence of the NNMT gene promoter region is shown in SEQ ID NO:1.

[0195] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region comprises the methylation level of DNA CpG sites in the region from 1050 bp before the transcription start site to 499 bp after the transcription start site of the NNMT gene.

[0196] In another preferred example, the region from 1050 bp before the transcription initiation site of the NNMT gene to 499 bp after the transcription initiation site corresponds to positions 951 to 2500 of the nucleotide sequence shown in SEQ ID NO:1.

[0197] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region comprises the methylation level of DNA CpG sites in the region from 1050 bp before the transcription start site to 193 bp before the transcription start site of the NNMT gene.

[0198] In another preferred example, the region from 1050 bp before the transcription initiation site of the NNMT gene to 193 bp before the transcription initiation site corresponds to positions 951 to 1808 of the nucleotide sequence shown in SEQ ID NO:1.

[0199] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region comprises the methylation level of DNA CpG sites in the region from 840 bp before the transcription start site to 469 bp before the transcription start site of the NNMT gene.

[0200] In another preferred example, the region from 840 bp before the transcription initiation site of the NNMT gene to 469 bp before the transcription initiation site corresponds to positions 1161 to 1532 of the nucleotide sequence shown in SEQ ID NO:1.

[0201] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region includes the methylation level of DNA CpG sites within a region between any two of positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050, and 114166066 on human chromosome 11 (including these two positions themselves).

[0202] In another preferred embodiment, the methylation level of the DNA CpG site in the NNMT gene region includes the methylation level of one or more (e.g., 2, 3, 4, 5, 6 or 7) sites among positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050 and 114166066 of human chromosome 11.

[0203] In another preferred embodiment, the methylation level of the DNA CpG site of the NNMT gene region comprises the methylation level of a site selected from position 114165695 of human chromosome 11, position 114165730 of human chromosome 11, position 114165769 of human chromosome 11, position 114165804 of human chromosome 11, position 114165938 of human chromosome 11, position 114166050 of human chromosome 11, position 114166066 of human chromosome 11, or a combination thereof.

[0204] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region includes the methylation level of DNA CpG sites within the region between any two of positions 1161, 1196, 1235, 1270, 1404, 1516 and 1532 of the nucleotide sequence of SEQ ID NO:1 (including these two positions themselves).

[0205] In another preferred embodiment, the methylation level of the NNMT gene region DNA CpG sites includes the methylation levels of one or more (e.g., 2, 3, 4, 5, 6 or 7) of the sites at positions 1161, 1196, 1235, 1270, 1404, 1516 and 1532 of the nucleotide sequence of SEQ ID NO:1.

[0206] In another preferred embodiment, the methylation level of the NNMT gene region DNA CpG site comprises the methylation level of a site selected from the sites at positions 1161, 1196, 1235, 1270, 1404, 1516, 1532 or combinations thereof in the sequence of SEQ ID NO:1.

[0207] In another preferred embodiment, the tumor is selected from lung cancer, kidney cancer, breast cancer, colon cancer, lymphoma, leukemia, pancreatic cancer, brain cancer, liver cancer, prostate cancer, or a combination thereof.

[0208] In another preferred embodiment, the lung cancer is selected from non-small cell lung cancer, small cell lung cancer, or a combination thereof.

[0209] In another preferred embodiment, the colon cancer comprises colon adenocarcinoma.

[0210] In another preferred embodiment, the lymphoma is selected from B cell lymphoma, T cell lymphoma, or a combination thereof.

[0211] In another preferred embodiment, the lymphoma comprises diffuse large B-cell lymphoma.

[0212] In another preferred embodiment, the brain tumor is selected from glioblastoma, glioma, medulloblastoma, neuroblastoma, or a combination thereof.

[0213] In another preferred embodiment, the brain medulloblastoma comprises a cerebellar medulloblastoma.

[0214] In another preferred embodiment, the glioblastoma comprises glioblastoma multiforme.

[0215] In another preferred embodiment, the brain tumor comprises a medulloblastoma.

[0216] In another preferred embodiment, the renal cancer is selected from renal clear cell adenocarcinoma, renal cancer Wilms, or a combination thereof.

[0217] In another preferred embodiment, the renal cancer comprises renal clear cell adenocarcinoma.

[0218] In another preferred embodiment, the renal cancer comprises Wilms renal cancer.

[0219] In another preferred embodiment, the renal cancer cancer cells comprise renal cancer Wilms cells.

[0220] In another preferred embodiment, the leukemia is selected from T lymphocytic leukemia, myeloid leukemia, or a combination thereof.

[0221] In another preferred embodiment, the T lymphocytic leukemia comprises acute T lymphocytic leukemia.

[0222] In another preferred embodiment, the myeloid leukemia comprises M4 AML acute myeloid leukemia.

[0223] In another preferred embodiment, the myeloid leukemia comprises FAB M4 AML acute myeloid leukemia.

[0224] In another preferred embodiment, said expression comprises protein expression and / or mRNA expression.

[0225] In another preferred embodiment, the composition is a pharmaceutical composition.

[0226] In another preferred embodiment, the composition or formulation further comprises a pharma- ceutically acceptable carrier.

[0227] In another preferred embodiment, said expression is mRNA expression or protein expression.

[0228] In another preferred embodiment, the composition or formulation is in the form of a solid, liquid or semi-solid.

[0229] In another preferred embodiment, the composition or preparation is an oral preparation, an external preparation, or an injectable preparation.

[0230] In another preferred embodiment, the composition or preparation is in the form of a tablet, an injection, an infusion, an ointment, a gel, a solution, a pill, or a coating.

[0231] A second aspect of the present invention provides a marker for determining whether a compound of formula I according to the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, is suitable for the prophylaxis and / or treatment of a tumor patient, the marker comprising a methylation level of the NNMT gene and / or a DNA CpG site in the NNMT gene region.

[0232] In another preferred embodiment, the marker comprises an expression level of the NNMT gene, an expression level of DNA methyltransferase, an expression level of UHRF1, a methylation level of a nucleotide site of the NNMT gene and / or a methylation level of a DNA CpG site in the NNMT gene region.

[0233] In another preferred embodiment, the marker comprises the NNMT gene, DNA methyltransferase, UHRF1, a nucleotide site of the NNMT gene and a DNA CpG site in the NNMT gene region.

[0234] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region includes the methylation level of DNA CpG sites in the NNMT gene promoter region.

[0235] In another preferred example, when the tumor cells of a tumor patient have low or no expression of the NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of nucleotide sites of the NNMT gene, and / or hypermethylation of DNA CpG sites in the NNMT gene region, the compound of formula I according to the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, becomes suitable for the prevention and / or treatment of the tumor patient.

[0236] In another preferred embodiment, high expression of the NNMT gene, low expression of DNA methyltransferase, low expression of UHRF1, low methylation of nucleotide sites of the NNMT gene, and / or low methylation of DNA CpG sites in the NNMT gene region in tumor cells of a tumor patient renders the compound of formula I according to the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, unsuitable for the prevention and / or treatment of the tumor patient.

[0237] In another preferred embodiment, the meaning that the compound of formula I as defined in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, is suitable for the prophylaxis and / or treatment of the tumor patient includes the meaning that the tumor cells of the tumor patient are sensitive to the compound of formula I as defined in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof.

[0238] In another preferred embodiment, the meaning that the compound of formula I as defined in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, is not suitable for the prophylaxis and / or treatment of the tumor patient includes the meaning that the tumor cells of the tumor patient are insensitive to the compound of formula I as defined in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma-ceutically acceptable salt thereof.

[0239] In another preferred embodiment, the tumor in which the NNMT gene is under-expressed or not expressed is a tumor as described in the first aspect of the present invention.

[0240] In another preferred embodiment, the tumor in which said DNA methyltransferase (eg DNMT1) is highly expressed is a tumor as described in the first aspect of the present invention.

[0241] In another preferred embodiment, said tumor in which UHRF1 is highly expressed is a tumor as described in the first aspect of the present invention.

[0242] In another preferred embodiment, the tumour in which said nucleotide site of the NNMT gene is hypermethylated is a tumour as described in the first aspect of the invention.

[0243] In another preferred embodiment, the tumor in which said NNMT gene region DNA CpG sites are hypermethylated is a tumor as described in the first aspect of the present invention.

[0244] In another preferred example, a tumor in which the NNMT gene is highly expressed refers to a tumor in which the ratio (E1 / E0) between the expression level E1 of the NNMT gene in a certain cell (e.g., a tumor cell) and the expression level E0 of the NNMT gene in the same cell or a normal cell (e.g., a cancerous bladder tissue cell) is >1.0, preferably ≧1.2 or ≧1.5, and more preferably ≧2, ≧3, ≧5, ≧8, ≧10, ≧15, ≧20, ≧30 or ≧50.

[0245] In another preferred embodiment, the tumor in which the DNA methyltransferase is underexpressed refers to a tumor in which the ratio (A1 / A0) between the expression level A1 of the DNA methyltransferase in tumor cells and the expression level A0 of the DNA methyltransferase in the same cells or normal cells (e.g., cancerous bladder tissue cells) is <1.0, preferably ≦0.7, and more preferably ≦0.6, ≦0.5, ≦0.4, ≦0.3, ≦0.2, ≦0.1, ≦0.05, ≦0.01, ≦0.005, ≦0.001, ≦0.0001, ≦0.00001, ≦0.000001 or ≦0.0000001.

[0246] In another preferred example, the tumor in which UHRF1 is underexpressed refers to a tumor in which the ratio (F1 / F0) between the expression level F1 of UHRF1 in tumor cells and the expression level F0 of UHRF1 in the same cells or normal cells (e.g., cancerous bladder tissue cells) is <1.0, preferably ≦0.7, and more preferably ≦0.6, ≦0.5, ≦0.4, ≦0.3, ≦0.2, ≦0.1, ≦0.05, ≦0.01, ≦0.005, ≦0.001, ≦0.0001, ≦0.00001, ≦0.000001 or ≦0.0000001.

[0247] In another preferred embodiment, a tumor in which the nucleotide site of the NNMT gene is hypomethylated refers to a tumor in which the ratio (L1 / L0) between the methylation level L1 of the nucleotide site of the NNMT gene in a certain cell (e.g., a tumor cell) and the methylation level L0 of the nucleotide site of the NNMT gene in the same cell or a normal cell (e.g., a cancerous bladder tissue cell) is <1.0, preferably ≦0.7, and more preferably ≦0.6, ≦0.5, ≦0.4, ≦0.3, ≦0.2, ≦0.1, ≦0.05, ≦0.01, ≦0.005, ≦0.001, ≦0.0001, ≦0.00001, ≦0.000001 or ≦0.0000001.

[0248] In another preferred embodiment, the tumor in which the DNA CpG site of the NNMT gene region is hypomethylated refers to a tumor in which the ratio (W1 / W0) between the methylation level W1 of the DNA CpG site of the NNMT gene region of a certain cell (e.g., a tumor cell) and the methylation level W0 of the DNA CpG site of the NNMT gene region of the same cell or a normal cell (e.g., a cancerous bladder tissue cell) is <1.0, preferably ≦0.7, and more preferably ≦0.6, ≦0.5, ≦0.4, ≦0.3, ≦0.2, ≦0.1, ≦0.05, ≦0.01, ≦0.005, ≦0.001, ≦0.0001, ≦0.00001, ≦0.000001 or ≦0.0000001.

[0249] A third aspect of the present invention provides a detection kit, comprising: (i) A detection reagent is provided for detecting the expression level of the NNMT gene and / or the methylation level of DNA CpG sites in the NNMT gene region.

[0250] In another preferred embodiment, the detection kit comprises: (i) A detection reagent is provided for detecting the expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of a nucleotide site in the NNMT gene, and / or the methylation level of a DNA CpG site in the NNMT gene region.

[0251] In another preferred embodiment, the detection sample of the detection kit includes tumor cells.

[0252] In another preferred embodiment, NNMT gene expression refers to the mRNA expression and / or protein expression of said gene.

[0253] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region comprises the methylation level of DNA CpG sites in the NNMT gene promoter region.

[0254] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region refers to the methylation level of DNA CpG sites within the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site.

[0255] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region refers to the methylation level of DNA CpG sites in the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site.

[0256] In another preferred embodiment, the methylation level of DNA CpG sites in the NNMT gene region refers to the methylation level of DNA CpG sites in the region from 840 bp before the transcription start site of the NNMT gene to 469 bp before the transcription start site.

[0257] A fourth aspect of the present invention provides the use of a detection kit according to the third aspect of the present invention for the manufacture of a companion detection kit for determining whether a compound of formula I according to the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, is suitable for the prophylaxis and / or treatment of a tumor patient.

[0258] In another preferred embodiment, the companion detection kit further comprises an instruction manual or label.

[0259] In another preferred embodiment, the instructions or label include: The present invention provides that when the tumor cells of a tumor patient have low or no expression of the NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of nucleotide sites of the NNMT gene, and / or hypermethylation of DNA CpG sites in the NNMT gene region, the compound of formula I according to the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, becomes suitable for the prevention and / or treatment of the tumor patient.

[0260] In another preferred embodiment, the instructions or label state that high expression of the NNMT gene, low expression of DNA methyltransferase, low expression of UHRF1, hypomethylation of nucleotide sites in the NNMT gene, and / or hypomethylation of DNA CpG sites in the NNMT gene region in tumor cells of a tumor patient renders the compound of formula I described in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, unsuitable for the prevention and / or treatment of the tumor patient.

[0261] In another preferred embodiment, the compound of formula I as defined in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, suitable for the prophylaxis and / or treatment of tumor patients is as defined in the second aspect of the present invention.

[0262] In another preferred embodiment, the meaning in which the compound of formula I as defined in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof is not suitable for the prophylaxis and / or treatment of tumor patients is as defined in the second aspect of the present invention.

[0263] A fifth aspect of the present invention provides a medical kit comprising: (i) a detection reagent used to detect the expression level of the NNMT gene and / or the methylation level of the DNA CpG site in the NNMT gene region; (ii) a compound of formula I as defined in the first aspect of the invention above, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof.

[0264] In another preferred embodiment, the medical kit comprises: (i) a detection reagent used to detect the expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of the nucleotide site of the NNMT gene, and / or the methylation level of the DNA CpG site in the NNMT gene region; (ii) a compound of formula I as defined in the first aspect of the invention above, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof.

[0265] In another preferred embodiment, the medical kit further comprises instructions or a label.

[0266] In another preferred embodiment, the instructions or label state that when low or no expression of the NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of nucleotide sites in the NNMT gene, and / or hypermethylation of DNA CpG sites in the NNMT gene region in tumor cells of a tumor patient, the compound of formula I described in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, becomes suitable for the prevention and / or treatment of the tumor patient.

[0267] In another preferred embodiment, the instructions or label state that high expression of the NNMT gene, low expression of DNA methyltransferase, low expression of UHRF1, low methylation of nucleotide sites in the NNMT gene, and / or low methylation of DNA CpG sites in the NNMT gene region in tumor cells of a tumor patient renders the compound of formula I described in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, unsuitable for the prevention and / or treatment of the tumor patient.

[0268] A sixth aspect of the present invention provides a method for the prevention and / or treatment of tumors comprising administering to a subject a compound of formula I as defined in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof.

[0269] In another preferred embodiment, the tumor is a tumor as described in the first aspect of the invention.

[0270] In another preferred embodiment, the subject's tumor comprises a tumor in which the NNMT gene is underexpressed or not expressed.

[0271] In another preferred embodiment, the subject's tumor comprises a tumor in which DNA methyltransferase is highly expressed.

[0272] In another preferred embodiment, the subject's tumor comprises a tumor in which UHRF1 is highly expressed.

[0273] In another preferred embodiment, the subject's tumor comprises a tumor in which the nucleotide site in the NNMT gene is hypermethylated.

[0274] In another preferred embodiment, the subject's tumor comprises a tumor in which NNMT gene region DNA CpG sites are hypermethylated.

[0275] A seventh aspect of the present invention provides an apparatus or system comprising: (i) a detection module used to detect the expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of the nucleotide site of the NNMT gene, and / or the methylation level of the DNA CpG site in the NNMT gene region; (ii) an output module; The output module includes: information that, in tumor cells of a tumor patient, low or no expression of the NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of nucleotide sites of the NNMT gene, and / or hypermethylation of DNA CpG sites in the NNMT gene region, the compound of formula I as described in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, becomes suitable for the prevention and / or treatment of the tumor patient; and / or When high expression of the NNMT gene, low expression of DNA methyltransferase, low expression of UHRF1, hypomethylation of nucleotide sites of the NNMT gene, and / or hypomethylation of DNA CpG sites in the NNMT gene region in tumor cells of a tumor patient occurs, information is output that the compound of formula I described in the first aspect of the present invention, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof becomes unsuitable for the prevention and / or treatment of the tumor patient.

[0276] In another preferred embodiment, the device comprises a gene detector or a protein detector.

[0277] In another preferred embodiment, the device or system further comprises a sample delivery module.

[0278] In another preferred embodiment, the sample supply module is used to supply a tumor cell extract.

[0279] In another preferred embodiment, the device or system further comprises a data processing module.

[0280] In another preferred embodiment, the data processing module processes the expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of a nucleotide site of the NNMT gene and / or the methylation level of a DNA CpG site in the NNMT gene region to obtain their numerical ranges.

[0281] In another preferred embodiment, the data processing module processes the expression level of the NNMT gene and / or the methylation level of DNA CpG sites in the NNMT gene promoter region to obtain their numerical ranges.

[0282] In another preferred embodiment, the data processing module processes the expression level of the NNMT gene and / or the methylation level of DNA CpG sites within the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site to obtain their numerical ranges.

[0283] In another preferred embodiment, the data processing module processes the expression level of the NNMT gene and / or the methylation level of DNA CpG sites within the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site to obtain their numerical ranges.

[0284] In another preferred embodiment, the data processing module processes the expression level of the NNMT gene and / or the methylation level of DNA CpG sites within the region from 840 bp before the transcription start site of the NNMT gene to 469 bp before the transcription start site to obtain their numerical ranges.

[0285] An eighth aspect of the present invention provides a compound of formula I, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof; [ka] Here, R1, R2, R3, R4, R5, R6, R7, R8, R 9、 R 10 , R 11 , R 12 , R 13 and R 14 is as described in the first aspect of the invention.

[0286] In another preferred embodiment, the compound of formula I is as described in the first aspect of the invention.

[0287] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula I-4: [ka] where A is O or S; W stands for O or S; R1, R4, R5, R6, R7, R8, R9, R 12 , R 10 , R 11 , R 13 and R 14 is defined as in the first aspect of the invention.

[0288] In another preferred embodiment, R1, R4, R 10 , R 11 , R 12 and R 13 each independently represents a hydrogen atom, a substituted or unsubstituted C1-C6 alkyl group, a substituted or unsubstituted C1-C6 alkoxyl group, or a substituted or unsubstituted C1-C6 alkylthiol group.

[0289] In another preferred embodiment, R5, R6, R7, R8, R9 and R 14 each independently represents a hydrogen atom.

[0290] Another favorable example is R 10 is a hydrogen atom or R 17 -A- stands for; Here A stands for O or S; R 17 represents a substituted or unsubstituted C3-C6 alkyl group, a C2-C4 alkenyl group -C1-C2 alkyl group-, or a C2-C8 ester group -C1-C2 alkyl group-.

[0291] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula I-1: [ka] Here A stands for O or S; R1, R4, R5, R6, R7, R8, R9, R 12 , R 10 , R11 , R 13 and R 14 is defined as in the first aspect of the invention.

[0292] Another favorable example is R 10 is a hydrogen atom or R 17 -A- stands for; Here A stands for O or S; R 17 represents a substituted or unsubstituted C3-C6 alkyl group, a C2-C4 alkenyl group -C1-C2 alkyl group-, or a C2-C8 ester group -C1-C2 alkyl group-.

[0293] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula: [ka]

[0294] In another preferred embodiment, the structure of the compound of formula I is shown in the following formula: [ka]

[0295] A ninth aspect of the invention provides a pharmaceutical composition comprising a compound of formula I as defined in the eighth aspect of the invention above, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, and a pharma- ceutically acceptable carrier.

[0296] It should be understood that within the scope of the present invention, the above technical features of the present invention, when combined with the following specific technical features (e.g., embodiments), will constitute new or preferred technical solutions, which will not be repeated here due to the limited size of the full text. [Brief description of the drawings]

[0297]

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[0298] As a result of long-term and in-depth research, the present inventors have unexpectedly found for the first time that the compounds of the present invention have obvious inhibitory effects on tumor cells with low (or no) expression of the NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of the nucleotide site of the NNMT gene and / or hypermethylation of the DNA CpG site in the NNMT gene region. The expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of the nucleotide site of the NNMT gene and / or the methylation level of the DNA CpG site in the NNMT gene promoter region serve as markers for determining whether the compounds of the present invention are suitable for the prevention and / or treatment of tumor patients. The present inventors have achieved the present invention based on this.

[0299] term As used herein, the terms "including," "comprising," and "having" may be used interchangeably and have closed, semi-closed, and open definitions. In other words, the terms include the meanings "consisting of" and "consisting essentially of."

[0300] As used herein, "there is hypermethylation of a DNA CpG site," "hypermethylate a DNA CpG site," and "a DNA CpG site is hypermethylated" may be used interchangeably.

[0301] As used herein, "there is hypomethylation of a DNA CpG site," "to hypomethylate a DNA CpG site," and "a DNA CpG site is hypomethylated" may be used interchangeably.

[0302] As used herein, "IC50" and "IC 50 The term "50% inhibitory concentration" may be used interchangeably and refers to the concentration of an inhibitor at which 50% inhibitory effect is achieved.

[0303] As used herein, "methylation of DNA CpG sites," "methylation of CpG nucleotides," and "CpG methylation" may be used interchangeably.

[0304] As used herein, the term "P / S" refers to the addition of Penicillin and Streptomycin to the relevant media.

[0305] As used herein, the term "a cell" refers to a single cell (e.g., a single cancer cell) or a group of cells that includes multiple similar cells (e.g., tumor tissue).

[0306] As used herein, "the compound of the present invention is suitable for a tumor patient" means that the tumor of the tumor patient is sensitive to the compound of the present invention, and so on.

[0307] As used herein, "the compounds of the present invention are not suitable for tumor patients" means that the tumors of the tumor patients are insensitive to the compounds of the present invention, and the like.

[0308] As used herein, "the expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of the nucleotide site of the NNMT gene and / or the methylation level of the DNA CpG site in the NNMT gene region" refers to one or more of the expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of the nucleotide site of the NNMT gene and the methylation level of the DNA CpG site in the NNMT gene region.

[0309] As used herein, "low or absent expression of the NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of nucleotide sites in the NNMT gene, and / or hypermethylation of DNA CpG sites in the NNMT gene region" refers to one or more of low or absent expression of the NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of nucleotide sites in the NNMT gene, and hypermethylation of DNA CpG sites in the NNMT gene region.

[0310] As used herein, "high expression of the NNMT gene, low expression of DNA methyltransferase, low expression of UHRF1, hypomethylation of nucleotide sites in the NNMT gene, and / or hypomethylation of DNA CpG sites in the NNMT gene region" refers to one or more of high expression of the NNMT gene, low expression of DNA methyltransferase, low expression of UHRF1, hypomethylation of nucleotide sites in the NNMT gene, and hypomethylation of DNA CpG sites in the NNMT gene region.

[0311] As used herein, the English name of the term "NNMT" is Nicotinamide N-Methyltransferase.

[0312] As used herein, the term "bp" refers to base pair.

[0313] As used herein, the term "SST" refers to the transcription start site.

[0314] As used herein, the term "Chr11" refers to human chromosome 11 as defined according to the human genome version GCF_000001405.25 (GRCh37.p13).

[0315] As used herein, the term "human chromosome 11" refers to human chromosome 11 defined according to the human genome version GCF_000001405.25 (GRCh37.p13).

[0316] As used herein, the terms "before the transcription start site" and "after the transcription start site" do not include the transcription start site itself.

[0317] As used herein, "position 114165695 of human chromosome 11" refers to the nucleotide at position 114165695 of human chromosome 11; "position 114165730 of human chromosome 11" refers to the nucleotide at position 114165730 of human chromosome 11; "position 114165769 of human chromosome 11" refers to the nucleotide at position 114165769 of human chromosome 11; "position 114165804 of human chromosome 11" refers to the nucleotide at position 114165804 on human chromosome 11; "position 114165938 on human chromosome 11" refers to the nucleotide at position 114165938 on human chromosome 11; "position 114166050 on human chromosome 11" refers to the nucleotide at position 114166050 on human chromosome 11; and "position 114166066 on human chromosome 11" refers to the nucleotide at position 114166066 on human chromosome 11.

[0318] As used herein, gene expression includes protein expression of the gene and / or mRNA expression of the gene, and the like.

[0319] As used herein, the term "DNMT3a" refers to DNA methyltransferase 3a.

[0320] As used herein, the term "DNMT3b" refers to DNA methyltransferase 3b.

[0321] As used herein, the term "DNMT1" refers to DNA methyltransferase 1.

[0322] As used herein, the term "UHRF1" refers to ubiquitin-related tau protein 1 that contains a PHD and a RING finger domain.

[0323] It should be understood that those skilled in the art can select the substituents and substitution patterns on the compounds of the present invention to produce chemically stable compounds, and can synthesize said compounds using techniques known in the art and the methods described below. When substituted with one or more (multiple) substituents, it should be understood that these substituents can be located on the same carbon or on different carbons, as long as a stable structure is produced.

[0324] As used herein, the terms "substitution" or "substituted" refer to the replacement of hydrogen atoms on a group with non-hydrogen groups as necessary to satisfy their valences, and which produce chemically stable compounds, i.e., compounds that do not spontaneously undergo transformations such as cyclization or elimination.

[0325] As used herein, "R", "R1" and "R 1 " have the same meaning and may be used interchangeably, and other similar definitions have the same meaning. As used herein, [ka] represents the bonding site of the atomic group.

[0326] As used herein, the term "alkyl group" refers to a linear (i.e., unbranched) or branched saturated hydrocarbon group containing only carbon atoms, or a combination of linear and branched groups. A carbon number specification preceding the alkyl group (e.g., C1-C6 alkyl group) indicates that the alkyl group has 1 to 6 carbon atoms, e.g., C1-C4 alkyl group indicates an alkyl group containing 1 to 4 carbon atoms. Representative examples of these alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, t-butyl, or similar groups.

[0327] As used herein, the term "C2-C4 alkenyl group" refers to a hydrocarbyl group formed by a linear or branched alkene molecule of 2 to 4 carbon atoms having one or more double bonds, by the loss of one hydrogen atom attached to the double bond. Representative examples thereof include vinyl groups (CH2=CH-), (C(CH3)2=CH-), or similar groups.

[0328] As used herein, the term "C2-C4 alkynyl group" refers to a hydrocarbyl group formed by a linear or branched alkene molecule of two to four carbon atoms having one or more triple bonds, by the loss of one hydrogen atom attached to the triple bond. Representative examples thereof include ethynyl groups (CH≡CH-), (HC-C≡CH-), or similar groups.

[0329] In the present invention, a "halogen atom" refers to F, Cl, Br or I.

[0330] In the present invention, "halogenated" refers to replacement with a halogen atom.

[0331] As used herein, the term "halogenated alkyl group" refers to an alkyl group in which one or more (preferably one, two, three or four) hydrogen atoms are replaced with halogen atoms. The alkyl group and halogen atoms are as defined above. The carbon number specified before the halogenated alkyl group (e.g., C1-C8 halogenated alkyl group) refers to the halogenated alkyl group having 1 to 8 carbon atoms, for example, C1-C6 halogenated alkyl group refers to a halogenated alkyl group containing 1 to 6 carbon atoms. Representative examples of these halogenated alkyl groups include, but are not limited to, -CF3, -CHF2, monofluorinated isopropyl group, difluorinated butyl group or similar atomic groups.

[0332] As used herein, the term "cycloalkyl ring" refers to a saturated or partially saturated monocyclic, bicyclic or polycyclic (fused, bridged or spiro) ring system. A carbon number specification (e.g., C3-C12) before a cycloalkyl ring indicates that the cycloalkyl ring has 3 to 12 ring carbon atoms. In some preferred embodiments, the term "C3-C8 cycloalkyl ring" refers to a saturated or partially saturated monocycloalkyl or dicycloalkyl ring having 3 to 8 ring carbon atoms, including cyclopropyl, cyclobutyl, cycloamyl, cycloheptyl or similar rings. A "spirocycloalkyl ring" refers to a bicyclic or polycyclic ring sharing one carbon atom (called a spiro atom) between monocyclic rings, which may contain one or more double bonds, but none of the rings has a completely conjugated pi-electron system. "Fused cycloalkyl ring" refers to an all-carbon atom bicyclic or polycyclic ring in which each ring in the system shares an adjacent pair of carbon atoms with another ring in the system, where one or more rings may contain one or more double bonds, but none of the rings has a complete conjugated π-electron system. "Bridged cycloalkyl ring" refers to an all-carbon atom polycyclic ring in which any two rings share two carbon atoms that are not directly connected, where such rings may contain one or more double bonds, but none of the rings has a complete conjugated π-electron system. Representative examples of these cycloalkyl rings include, but are not limited to, cyclopropyl, cyclobutyl, cycloamyl, cycloheptyl, or the like.

[0333] As used herein, the term "cycloalkyl group" refers to a saturated or partially saturated monocyclic, bicyclic or polycyclic (fused, bridged or spiro) ring group. The carbon number specification before the cycloalkyl group (e.g., C3-C12) indicates that the cycloalkyl group has 3 to 12 ring carbon atoms, and in some preferred embodiments, the term "C3-C8 cycloalkyl group" refers to a saturated or partially saturated monocycloalkyl or dicycloalkyl group having 3 to 8 ring carbon atoms, including cyclopropyl, cyclobutyl, cycloamyl, cycloheptyl or similar groups. A "spirocycloalkyl group" refers to a bicyclic or polycyclic group that shares a carbon atom (called a spiro atom) between the monocyclic rings, and such groups may contain one or more double bonds, but none of the groups has a completely conjugated pi-electron system. "Fused cycloalkyl group" refers to a bicyclic or polycyclic group of all carbon atoms in which each ring in the system shares an adjacent pair of carbon atoms with another ring in the system, where one or more of the rings may contain one or more double bonds, but neither ring has a complete conjugated pi-electron system. "Bridged cycloalkyl group" refers to a polycyclic group of all carbon atoms in which any two rings share two carbon atoms that are not directly connected, where such group may contain one or more double bonds, but neither ring has a complete conjugated pi-electron system. Representative examples of these cycloalkyl groups are: [ka] Including, but not limited to:

[0334] As used herein, the term "halogenated cycloalkyl group" refers to a cycloalkyl group in which one or more (preferably one, two, three or four) hydrogen atoms are replaced with halogen atoms. The cycloalkyl group and halogen atoms are as defined above. The carbon number specified before the cycloalkyl group (e.g., C3-C8 halogenated cycloalkyl group) refers to the cycloalkyl group having 3 to 8 ring carbon atoms, for example, C3-C8 halogenated cycloalkyl group refers to a halogenated cycloalkyl group containing 3 to 8 ring carbon atoms. Representative examples of these halogenated cycloalkyl groups include, but are not limited to, monofluorinated cyclopropyl group, monochlorinated cyclobutyl group, monofluorinated cycloamyl group, difluorinated cycloheptyl group or similar atomic groups.

[0335] The term "alkoxyl group" refers to the RO-group, where R is an alkyl group. Alkyl groups are as defined above. The carbon number specified before the alkoxyl group (e.g., C1-C8 alkoxyl group) indicates that the alkyl group in the alkoxyl group has 1 to 8 carbon atoms. Representative examples of these alkoxyl groups include, but are not limited to, methoxy, ethoxy, N-propoxy, isopropoxy, t-butoxy, or similar groups.

[0336] As used herein, the term "alkylthiol group" refers to an R-S group, where R is an alkyl group. The alkyl group is as defined above. The carbon number specified before the alkylthiol group (e.g., C1-C8 alkoxyl group) indicates that the alkyl group in the alkylthiol group has 1 to 8 carbon atoms. Representative examples of these alkylthiol groups include, but are not limited to, methylthio, ethylthio, N-propylthio, isopropylthio, t-butylthio, or similar groups.

[0337] The term "cycloalkoxyl group" refers to the group RO- where R is a cycloalkyl group. Cycloalkyl groups are as defined above. The carbon number specified before the cycloalkoxyl group (e.g., C3-C8 cycloalkoxyl group) indicates that the cycloalkyl group in the cycloalkoxyl group has 3 to 8 carbon atoms. Representative examples of these cycloalkoxyl groups include, but are not limited to, cyclopropoxy, cyclobutoxy, or similar groups.

[0338] The term "cycloalkylthiol group" refers to an RS-atom, where R is a cycloalkyl group. Cycloalkyl groups are as defined above. The carbon number specified before the cycloalkylthiol group (e.g., C3-C8 cycloalkoxyl group) indicates that the cycloalkyl group in the cycloalkylthiol group has 3 to 8 carbon atoms. Representative examples of these cycloalkylthiol groups include, but are not limited to, a cyclopropylthio group, a cyclobutylthio group, or a similar atomic group.

[0339] As used herein, the term "halogenated alkoxyl group" refers to a halogenated alkyl group -O-, where the halogenated alkyl group is as defined above. For example, a C1-C6 halogenated alkoxyl group refers to a halogenated alkoxyl group having 1 to 6 carbon atoms. Representative examples of these halogenated alkoxyl groups include, but are not limited to, monofluorinated methoxyl group, monofluorinated ethoxyl group, difluorinated butoxy group, or similar atomic groups.

[0340] As used herein, the term "halogenated alkylthiol group" refers to a halogenated alkyl group -S-. The halogenated alkyl group is as defined above. For example, a C1-C6 halogenated alkylthiol group refers to a halogenated alkylthiol group having 1 to 6 carbon atoms. Representative examples of these halogenated alkylthiol groups include, but are not limited to, a monofluorinated methylthio group, a monofluorinated ethylthio group, a difluorinated butylthiol group, or a similar atomic group.

[0341] The term "heterocycloalkyl ring", also referred to as "heterocycle", refers to a fully saturated or partially unsaturated ring (including, but not limited to, a 3- to 7-membered monocyclic ring, a 7- to 11-membered bicyclic ring, or an 8- to 16-membered tricyclic ring) in which at least one heteroatom is present in the ring having at least one carbon atom. The number of members qualifying the heterocycle refers to the number of ring atoms in the heterocycloalkyl ring. For example, a 3- to 16-membered heterocycle refers to a heterocycle having 3 to 16 ring atoms. In each heterocycle having a heteroatom, there may be one or more (e.g., 1, 2, 3, or 4) heteroatoms, each of which is independently selected from a nitrogen atom, an oxygen atom, or a sulfur atom, where the nitrogen atom or sulfur atom may be oxidized and the nitrogen atom may also be quaternized. The heterocycle may be bonded to any heteroatom or carbon atom residue of the ring or ring system molecule. Representative examples of these monocyclic heterocycloalkyl rings include, but are not limited to, azetidinyl, oxetane, imidazoline, imidazolidone, tetrahydrofuranyl, piperidinyl, piperazinyl, 2-oxypiperazinyl, 2-oxypiperidinyl, 4-piperidinone, tetrahydropyranyl, morpholine, thiomorpholine, thiomorpholine sulfoxide, thiomorpholine sulfone, 1,3-dioxane, tetrahydro-1,1-dioxythiophene, etc. Polycyclic heterocycloalkyl rings include spiro, fused, and bridged heterocycles. Related spiro, fused, and bridged heterocycles are optionally connected to other rings by a single bond or further fused to other cycloalkyl and heterocycles through any two or more atoms on the ring.

[0342] The term "heterocycloalkyl group" refers to a fully saturated or partially unsaturated cyclic group (including, but not limited to, a 3- to 7-membered monocyclic ring, a 7- to 11-membered bicyclic ring, or an 8- to 16-membered tricyclic ring) in which at least one heteroatom is present in a ring having at least one carbon atom. The number of members preceding a heterocycloalkyl group refers to the number of ring atoms in the heterocycloalkyl group. For example, a 3- to 16-membered heterocycloalkyl group refers to a heterocycloalkyl group having 3 to 16 ring atoms. In each heterocycle having a heteroatom, there may be one or more (e.g., 1, 2, 3, or 4) heteroatoms, each of which is independently selected from a nitrogen atom, an oxygen atom, or a sulfur atom, where the nitrogen atom or sulfur atom may be oxidized and the nitrogen atom may also be quaternized. The heterocycloalkyl group may be attached to the residue of any heteroatom or carbon atom of the ring or ring system molecule. Representative examples of these single-ring heterocycloalkyl groups include, but are not limited to, azetidinyl, oxetane, imidazoline, imidazolidone, tetrahydrofuranyl, piperidinyl, piperazinyl, 2-oxypiperazinyl, 2-oxypiperidinyl, 4-piperidinone, tetrahydropyranyl, morpholine, thiomorpholine, thiomorpholine sulfoxide, thiomorpholine sulfone, 1,3-dioxane, tetrahydro-1,1-dioxythiophene, and the like. Polycyclic heterocycloalkyl groups include spiro, fused, and bridged heterocyclic groups. Related spiro, fused, and bridged heterocycloalkyl groups are optionally connected to other atomic groups by single bonds or further fused to other cycloalkyl and heterocyclic rings through any two or more atoms on the ring.

[0343] The term "aryl ring" refers to an all carbon atom monocyclic or condensed polycyclic ring (rings sharing adjacent pairs of carbon atoms) having a conjugated π electron system, which is an aromatic cyclic hydrocarbon compound. The carbon number specified before the aryl ring (e.g., C6-C12 aryl group) indicates that the aryl ring has 6 to 12 ring carbon atoms. Representative examples of these aryl rings include phenyl rings and naphthoyl rings. The aryl ring can be condensed to other carbocyclic rings (including saturated or unsaturated rings), but it does not contain heteroatoms such as nitrogen atoms, oxygen atoms, or sulfur atoms, and the point of attachment of the main chain must be on a carbon atom on the ring of the conjugated π electron system. Representative examples of these aryl rings include phenyl rings, naphthoyl rings, or similar rings.

[0344] The term "aryl group" refers to an all-carbon atom monocyclic or fused polycyclic (rings sharing adjacent pairs of carbon atoms) atomic group having a conjugated π electron system, which is an atomic group of an aromatic cyclic hydrocarbon compound. The carbon number specified before the aryl group (e.g., C6-C12 aryl group) indicates that the aryl group has 6 to 12 ring carbon atoms. Representative examples of these aryl groups include phenyl and naphthoyl groups. The aryl group can be fused to other cyclic atomic groups (including saturated or unsaturated rings), but it does not contain heteroatoms such as nitrogen, oxygen, or sulfur atoms, and the point of attachment of the main chain must be on a carbon atom on the ring of the conjugated π electron system. Representative examples of these aryl groups are: [ka] Including, but not limited to:

[0345] The term "heteroaryl ring" refers to an aromatic heterocyclic ring having one or more (preferably one, two, three or four) heteroatoms. The ring may be a single ring (monocyclic) or multiple rings (bicyclic, tricyclic or polycyclic) that are fused or covalently linked, and each heterocyclic ring that contains a heteroatom may have one or more (e.g., one, two, three or four) heteroatoms independently selected from oxygen, sulfur and nitrogen atoms. The number of members in the heteroaryl ring refers to the number of ring atoms in the heteroaryl ring. For example, a 5-12 membered heteroaryl ring refers to a heteroaryl ring having 5 to 12 ring atoms. Representative examples of these heteroaryl rings include, but are not limited to, a pyrrolyl ring, a pyrazole ring, an imidazole ring, an oxazole ring, an isoxazole ring, a thiazole ring, a thiadiazole ring, an isothiazole ring, a furan ring, a pyridine ring, a pyrazine ring, a pyrimidine ring, a pyrazine ring, a triazine ring, a triazole ring, a tetrazolyl ring, and the like.

[0346] The term "heteroaryl group" refers to an aromatic heterocyclic ring system having one or more (preferably one, two, three or four) heteroatoms. The group may be a single ring (monocyclic) or multiple fused or covalently linked rings (bicyclic, tricyclic or polycyclic), and each heteroatom-containing heterocycle may have one or more (e.g., one, two, three or four) heteroatoms independently selected from oxygen, sulfur and nitrogen atoms. The number of members in the heteroaryl group refers to the number of ring atoms in the heteroaryl group. For example, a 5-12 membered heteroaryl group refers to a heteroaryl group having 5 to 12 ring atoms. Representative examples of these heteroaryl groups include, but are not limited to, pyrrolyl groups, pyrazole groups, imidazole groups, oxazole groups, isoxazole groups, thiazole groups, thiadiazole groups, isothiazole groups, furan groups, pyridine groups, pyrazine groups, pyrimidine groups, pyrazine groups, triazine groups, triazole groups, tetrazolyl groups, and the like.

[0347] As used herein, the term "carboxyl group" refers to a group of atoms of -COOH or -alkyl-COOH, where alkyl is as defined above. For example, a "C2-C4 carboxyl group" refers to a group of atoms of -C1-C3 alkyl-COOH. Representative examples of these carboxyl groups include, but are not limited to, -COOH, -CH2COOH, -C2H4COOH, or similar groups.

[0348] As used herein, the term "ester group" refers to a group of atoms of RC(O)-O- or -C(O)-OR, where alkyl group (R) is as defined above. For example, a "C2-C4 ester group" refers to a group of atoms of -C1-C3 alkyl group -C(O)-O- or a group of atoms of -C(O)-O-C1-C3 alkyl group. Representative examples of these ester groups include, but are not limited to, CH3COO-, C2H5COO-, C3H8COO-, (CH3)2CHCOO-, -COOCH3, -COOC2H5, -COOC3H8, -COOC(CH3)3, or similar groups.

[0349] As used herein, the term "acylamino group" refers to the group RC(O)-N- or -C(O)-NR, where the alkyl group (R) is as defined above. For example, a "C2-C4 acylamino group" refers to the group -C1-C3 alkyl group -C(O)-N- or the group -C(O)-N-C1-C3 alkyl group. Representative examples of these acylamino groups include, but are not limited to, CH3CO-N-, CH5CO-N-, CH8CO-N-, (CH3)2CHCO-N-, -CO-N-CH3, -CO-N-C2H5, -CO-N-C3H8 or similar groups.

[0350] As used herein, an "amino group" alone or as part of another substituent refers to -NH2.

[0351] As used herein, a "nitro group" alone or as part of another substituent refers to --NO.sub.2.

[0352] As used herein, a "cyan group" alone or as part of another substituent refers to -CN.

[0353] As used herein, a "hydroxyl group" alone or as part of another substituent refers to --OH.

[0354] As used herein, a "mercapto group" alone or as part of another substituent refers to -SH.

[0355] In this specification, all substituents are meant to be unsubstituted unless expressly stated as "substituted." The term "substituted" refers to a particular substituent replacing one or more hydrogen atoms on a particular atomic group. Particular substituents are those described above or appearing in each example. Preferably, the "substituted" refers to one or more (preferably one, two, three, four, five, six, seven or eight) hydrogen atoms on a ring or atomic group being replaced by a substituent selected from a C1-C8 alkyl group, a C3-C8 cycloalkyl group, a C1-C8 halogenated alkyl group, a C3-C8 halogenated cycloalkyl group, a halogen atom, a nitro group, -CN, a hydroxyl group, a mercapto group, an amino group, a C1-C4 carboxyl group, a C2-C4 ester group, a C2-C4 acylamino group, a C1-C8 alkoxyl group, a C1-C8 alkylthiol group, a C1-C8 halogenated alkoxyl group, a C1-C8 halogenated alkylthiol group, a C6-C12 aryl group, a 5-10 membered heteroaryl group and a 5-10 membered heterocycloalkyl group. Unless otherwise specified, an optionally substituted radical may bear a substituent selected from a specified group at any substitutable position of the radical, and said substituent may be the same or different at each position.

[0356] In the present invention, "prevention" refers to a method of preventing the onset of a disease and / or its associated symptoms or protecting a subject from morbidity. As used herein, "prevention" also refers to delaying the onset of a disease and / or its associated symptoms, as well as reducing the subject's risk of morbidity.

[0357] "Treatment" according to the present invention means slowing and terminating the progression of the disease or eliminating the disease, but does not require 100% inhibition, elimination or reversal. In some embodiments, the tumor and its complications are reduced, inhibited and / or reversed by at least about 10%, 30%, 50%, 80%, or 100%, etc. under the action of the compounds of the present invention, compared to levels observed in the absence of the compounds of the present invention.

[0358] compound As used herein, "a compound of the present invention," "isoquinoline compound of the present invention," "a compound of formula I of the present invention," or "a compound of formula I," may be used interchangeably, and refer to a compound having the structure of formula I, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof. This term should be understood to include mixtures of the above components. [ka]

[0359] Specifically, the compounds of formula I above are defined as in the first aspect of the invention.

[0360] According to the present study, the compounds of the present invention have more obvious inhibitory effect on tumor cells with low or no expression of NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of nucleotide site of NNMT gene and / or hypermethylation of DNA CpG site of NNMT gene region.Tumor cells with low expression of NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, hypermethylation of nucleotide site of NNMT gene and / or hypermethylation of DNA CpG site of NNMT gene region are sensitive to the compounds of the present invention.

[0361] The compounds of formula I of the present invention may form pharma- ceutically acceptable salts with acids in the cationic state.

[0362] The term "pharmaceutical acceptable salt" refers to a salt formed by a compound of the present invention and an acid and suitable for use as a medicament. Pharmaceutically acceptable salts include inorganic salts and organic salts. One type of preferred salt is a salt formed by a compound of the present invention and an acid, and suitable acids for forming such salts include, but are not limited to, inorganic acids such as hydrochloric acid, hydrobromic acid, hydrofluoric acid, sulfuric acid, nitric acid, and phosphoric acid, organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tartaric acid, citric acid, picric acid, methanesulfonic acid, benzenesulfonic acid, and benzenesulfonic acid, and acidic amino acids such as aspartic acid and glutamic acid.

[0363] The present invention may convert the compounds as shown in formula I into their pharma- ceutically acceptable salts in a conventional manner. For example, adding a solution of the corresponding acid to a solution of the compound and removing the entire salt after salification allows to obtain the corresponding salt of the compound of the present invention.

[0364] In a preferred embodiment of the present invention, the structure of the compound of formula I is shown in the following formula I-1: [ka] Here A stands for O or S; R1, R4, R5, R6, R7, R8, R9, R 12 , R 10 , R 11 , R 13 and R 14 is defined as in the first aspect of the invention; R 10 is a hydrogen atom or R 17 -A- stands for; Here A stands for O or S; R 17 represents a substituted or unsubstituted C3-C6 alkyl group, a C2-C4 alkenyl group -C1-C2 alkyl group-, or a C2-C8 ester group -C1-C2 alkyl group-.

[0365] Preferred compounds of the present invention are [ka] is selected from.

[0366] Representatively, preferred compounds of the invention are [ka] Selected from JPEG0007616583000034.jpg155147.

[0367] In another preferred embodiment, the berberine comprises berberine chloride or berberine sulfate.

[0368] NNMT gene In the present invention, the English name of NNMT is Nicotinamide N-Methyltransferase. Different databases have different identification numbers for NNMT gene, such as HGNC:7861; Entrez Gene:4837; Ensembl:ENSG00000166741; OMIM:600008; UniProtKB:P40261.

[0369] According to the human genome version GCF_000001405.25 (GRCh37.p13), the NNMT gene region is located from bp 114,128,528 to bp 114,184,258 on human chromosome 11, and is a DNA sequence with a total length of 55,731 bp. This region includes the NNMT gene promoter region, the NNMT gene exon region and the NNMT gene intron region, and the NNMT gene transcription start site is at bp 114,166,535.

[0370] The NNMT gene promoter region is the nucleotide sequence from bp 114,164,535 to bp 114,167,034 on human chromosome 11, i.e., the sequence from 2000 bp (inside the brackets) before the transcription start site of the NNMT gene to the transcription start site itself and 499 bp (underlined) after it. The NNMT gene promoter region is 2500 bp in length, and its nucleotide sequence is shown in SEQ ID NO:1.

[0371] SEQ ID NO:1: GAGGAGGTGCTTGCCAGACACTGGGTCATGGCAGTGGTCGGTGAAGCTGCAGTTGCCTAGGGCAGGGATGGAGAGAGAGTCTGGGCATGAGGAGAGGGTCTCGGGATGTTTGGCTGGACTAGATTTTACAGAAAGCCTTATCCAGGCTTTTAAAATTACTCTTTCCAGACTTCATCTGAGACTCCTTCTTCAGCCAACATTCCTTAGCCCTGAATACATTTCCTATCCTCATCTTTCCCTTCTTTTTTTTCCTTTCTTTTACATGTTTAAATTTAAACCATTCTTCGTGACCCCTTTTCTTGGGAGATTCATGGCAAGAACGAGAAGAATGATGGTGCTTGTTAGGGGATGTCCTGTCTCTCTGAACTTTGGGGTCCTATGCATTAAATAATTTTCCTGACGAGCTCAAGTGCTCCCTCTGGTCTACAATCCCTGGCGGCTGGCCTTCATCCCTTGGGCAAGCATTGCATACAGCTCATGGCCCTCCCTCTACCATACCC .

[0372] In the present invention, the region from 1050 bp before the transcription initiation site of the NNMT gene to 499 bp after the transcription initiation site corresponds to positions 951-2500 of the nucleotide sequence shown in SEQ ID NO:1.

[0373] In the present invention, the region from 1050 bp before the transcription initiation site of the NNMT gene to 193 bp before the transcription initiation site corresponds to positions 951-1808 of the nucleotide sequence shown in SEQ ID NO:1.

[0374] In the present invention, the region from 840 bp before the transcription initiation site of the NNMT gene to 469 bp before the transcription initiation site corresponds to positions 1161-1532 of the nucleotide sequence shown in SEQ ID NO:1.

[0375] In the present invention, the sites of the nucleotide sequence of SEQ ID NO: 1 corresponding to positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050 and 114166066 of human chromosome 11 are shown in Table 1, respectively. [Table 1]

[0376] DNA methylation DNA methylation is a form of chemical modification of DNA that alters gene expression without changing the DNA sequence. Many studies have shown that DNA methylation may modulate gene expression by altering chromatin structure, DNA morphology, DNA stability, and DNA-protein interaction patterns.

[0377] DNA methylation is one of the first and most extensively studied epigenetic regulators. In the broad sense, DNA methylation refers to the chemical modification process in which specific bases in DNA sequences acquire one methyl group via covalent bond with S-adenosyl methionine as the methyl donor under the catalysis of DNA methyltransferase 1. This DNA methylation modification can occur at the C-5 position of cytosine, the N-6 position of adenine, and the N-7 position of guanine. In general research, DNA methylation refers to the process in which the fifth carbon atom of cytosine in CpG dinucleotides is methylated. The product is called 5-methylcytosine (5-mC), which is the main form of DNA methylation in eukaryotes such as plants and animals. DNA methylation, as a relatively stable modification, can be inherited to new generations of DNA during the DNA replication process under the action of DNA methyltransferases, making it an important regulator of epigenetic inheritance.

[0378] DNA methylation reactions can be divided into two types: in the first type, DNA with two unmethylated strands is methylated, called de novo methylation, and in the second type, double-stranded DNA with one methylated strand is methylated on the other unmethylated strand, called maintenance methylation.

[0379] Typically, DNA methylation is the methylation of DNA CpG sites. CpG dinucleotides are distributed very unevenly in the human genome, and some segments of the genome have CpGs at higher than normal rates. Enriched regions of CpG sites (also called CpG islands) are mainly located in promoter and exon regions of genes, and some regions are enriched in CpG dinucleotides, among which more than 60% of gene promoters contain CpG islands. Here, CpG is an abbreviation of cytosine (C)-phosphate (p)-guanine (G).

[0380] Intracellular gene expression is subject to various types of regulation by signal transduction pathways, transcription factors, and epigenetic modifications. DNA methylation is an important method by which epigenetic modifications regulate gene expression. The DNA methylation level in a specific gene region always affects the expression level of that gene. DNA methylation, an epigenetic modification, has a more stable effect on gene expression and is less susceptible to the extracellular environment compared to the regulation of gene expression by signal transduction pathways and transcription factors. DNA methylation is an ideal biomarker because it can be easily detected by existing technologies.

[0381] use The present invention provides the use of the compounds of the invention in the prevention and / or treatment of tumors.

[0382] tumor According to the present study, the compounds of the present invention are useful for the prevention and / or treatment of tumors.

[0383] In the present invention, the terms "tumor," "carcinosis," "cancer," and "mass" may be used interchangeably.

[0384] In a preferred embodiment of the present invention, the "tumor" described in the present invention includes tumors in which the NNMT gene is underexpressed or not expressed. As a representative example, the tumors in which the NNMT gene is underexpressed or not expressed described in the present invention are as described in the first aspect of the present invention.

[0385] In a preferred embodiment of the present invention, the "tumor" according to the present invention includes a tumor in which DNA methyltransferase is highly expressed. As a representative example, the tumor in which DNA methyltransferase is highly expressed according to the present invention is as described in the first aspect of the present invention.

[0386] The DNA methyltransferase according to the present invention includes, but is not limited to, DNMT1, DNMT3a, DNMT3b, or a combination thereof. Preferably, the DNA methyltransferase according to the present invention includes DNMT1.

[0387] In a preferred embodiment of the present invention, the "tumor" according to the present invention includes a tumor in which DNMT1 is highly expressed. As a representative example, the tumor in which DNMT1 is highly expressed according to the present invention is as described in the first aspect of the present invention.

[0388] In a preferred embodiment of the present invention, the "tumor" according to the present invention includes a tumor in which DNMT3a is highly expressed. As a representative example, the tumor in which DNMT3a is highly expressed according to the present invention is as described in the first aspect of the present invention.

[0389] In a preferred embodiment of the present invention, the "tumor" according to the present invention includes a tumor in which DNMT3b is highly expressed. As a representative example, the tumor in which DNMT3b is highly expressed according to the present invention is as described in the first aspect of the present invention.

[0390] In a preferred embodiment of the present invention, the "tumor" according to the present invention includes a tumor in which UHRF1 (ubiquitin-related tau protein 1 containing PHD and ring finger domain) is highly expressed. As a representative example, the tumor in which UHRF1 according to the present invention is highly expressed is as described in the first aspect of the present invention.

[0391] In a preferred embodiment of the present invention, the "tumor" according to the present invention includes a tumor in which the nucleotide site of the NNMT gene is hypermethylated. As a representative example, the tumor in which the nucleotide site of the NNMT gene according to the present invention is hypermethylated is as described in the first aspect of the present invention.

[0392] In a preferred embodiment of the present invention, the "tumor" according to the present invention includes a tumor in which the NNMT gene region DNA CpG site is hypermethylated. As a representative example, the tumor in which the NNMT gene region DNA CpG site is hypermethylated according to the present invention is as described in the first aspect of the present invention.

[0393] As a more detailed example, the tumor according to the invention is as described in the first aspect of the invention.

[0394] In the present invention, representative tumor types corresponding to various tumor cell lines are shown in Table 2 below. [Table 2]

[0395] marker The present invention provides a marker for determining whether the compound of the present invention is suitable for the prevention and / or treatment of tumor patients, the marker comprising an expression level of the NNMT gene, an expression level of DNA methyltransferase, an expression level of UHRF1, a methylation level of a nucleotide site of the NNMT gene, and / or a methylation level of a DNA CpG site in the NNMT gene region.

[0396] In one embodiment, the expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of the nucleotide site of the NNMT gene and / or the methylation level of the DNA CpG site of the NNMT gene promoter region serve as markers for determining whether the compound of the present invention is suitable for the prevention and / or treatment of tumor patients. The method includes: In tumor cells of a tumor patient, when the NNMT gene is under-expressed or not expressed, the DNA methyltransferase is over-expressed, the UHRF1 is over-expressed, the nucleotide site of the NNMT gene is over-methylated, and / or the DNA CpG site of the NNMT gene region is over-methylated, the compound of the present invention is suitable for the prevention and / or treatment of a tumor patient; and / or This includes, but is not limited to, high expression of the NNMT gene, low expression of DNA methyltransferase, low expression of UHRF1, low methylation of nucleotide sites in the NNMT gene, and / or low methylation of DNA CpG sites in the NNMT gene region in tumor cells of a tumor patient, making the compounds of the present invention unsuitable for the prevention and / or treatment of tumor patients.

[0397] Specifically, tumors in which the NNMT gene is under-expressed or not expressed, tumors in which DNA methyltransferase (e.g., DNMT1) is highly expressed, tumors in which UHRF1 is highly expressed, tumors in which nucleotide sites in the NNMT gene are hypermethylated, and / or tumors in which DNA CpG sites in the NNMT gene region are hypermethylated are as described in the first aspect of the present invention.

[0398] Specifically, tumors in which the NNMT gene is highly expressed, tumors in which DNA methyltransferase (e.g., DNMT1) is underexpressed, tumors in which UHRF1 is underexpressed, tumors in which nucleotide sites in the NNMT gene are hypomethylated, and / or tumors in which DNA CpG sites in the NNMT gene region are hypomethylated are as described in the second aspect of the present invention.

[0399] The present invention further provides the use of said marker (or the expression level thereof) or detection agent, which is used to manufacture a detection kit, which is used to determine whether the compound of the present invention is suitable for the prevention and / or treatment of a tumor patient.

[0400] Compositions or formulations, active ingredient combinations and medical kits, and methods of administration Preferably, the composition according to the present invention is a pharmaceutical composition, and the composition according to the present invention may comprise a pharma- ceutically acceptable carrier.

[0401] As used herein, "a pharma- ceutically acceptable carrier" refers to one or more compatible solid, semi-solid, liquid, and gel fillers that must be suitable for human or animal use and have sufficient purity and low toxicity. "Compatibility" refers to the ability of each component in the drug composition to mix with the active ingredient of the drug, and to mix them with each other without significantly decreasing the efficacy of the drug.

[0402] In the present invention, it should be understood that the pharma- ceutically acceptable carrier is not particularly limited and may be selected from materials commonly used in the art, prepared by a conventional method, or purchased from the market. Some of the pharma-ceutically acceptable carriers include cellulose and its derivatives (e.g., methylcellulose, ethylcellulose, hydroxypropylmethylcellulose, sodium carboxymethylcellulose, etc.), gelatin, talc, solid lubricants (e.g., stearic acid and magnesium stearate), calcium sulfate, vegetable oils (e.g., soybean oil, sesame oil, peanut oil, olive oil, etc.), polyhydric alcohols (e.g., propylene glycol, glycerin, mannitol, sorbitol, etc.), emulsifiers (e.g., Tween), wetting agents (e.g., sodium lauryl sulfate), buffers, chelating agents, thickeners, pH adjusters, penetration enhancers, colorants, flavorings, stabilizers, antioxidants, preservatives, bacteriostatic agents, heat-free raw water, etc.

[0403] In a preferred embodiment of the present invention, the composition or formulation is in the form of a solid, liquid or semi-solid.

[0404] In a preferred embodiment of the present invention, the type of the composition or preparation is an oral preparation, an external preparation, or an injectable preparation.

[0405] Representative examples of the composition or preparation include tablets, injections, infusions, ointments, gels, solutions, pills, and coatings.

[0406] The drug formulation should be consistent with the dosage regimen. The drug of the present invention may also be used with other synergistic therapeutic drugs (before, during, or after use). When using a drug composition or formulation, a safe and effective amount of the drug is administered to the subject (e.g., a human or non-human mammal). The safe and effective amount is usually at least about 10 μg / kg of body weight, and in most cases, less than about 8 mg / kg of body weight, preferably about 10 μg / kg to about 1 mg / kg of body weight. Of course, the specific dosage should be determined in consideration of conditions such as the route of administration and the health condition of the patient, but these conditions are taken into account by a skilled physician.

[0407] The present invention has the following main beneficial effects:

[0408] The present invention provides biomarkers for precise dosing of the compounds of the present invention, and these biomarkers can effectively identify tumor patients who are sensitive to antitumor drugs, thereby improving the therapeutic efficacy and avoiding the dosing of these drugs to patients with tumors that are insensitive to antitumor drugs, thereby achieving precise application of these drugs.

[0409] Through a series of studies, the present invention unexpectedly finds for the first time that the expression level of the NNMT gene, the expression level of DNA methyltransferase, the expression level of UHRF1, the methylation level of the nucleotide site of the NNMT gene and / or the methylation level of the DNA CpG site in the NNMT gene promoter region can function as markers for determining whether the compound of the present invention is suitable for the prevention and / or treatment of tumor patients.

[0410] Tumors with low or no expression of NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, high methylation of nucleotide site of NNMT gene, and / or high methylation of DNA CpG site in NNMT gene region are highly sensitive to the compound of the present invention, that is, the compound of the present invention has excellent therapeutic effect on tumors with low or no expression of NNMT gene, high expression of DNA methyltransferase, high expression of UHRF1, high methylation of nucleotide site of NNMT gene, and / or high methylation of DNA CpG site in NNMT gene region. Moreover, the detection method of DNA CpG site methylation level has high completeness, stability and reliability, so it is suitable for developing molecular markers.

[0411] The present invention will now be further described in conjunction with specific examples. It should be understood that these embodiments are intended only to illustrate the present invention, without limiting the scope of the present invention. In the following examples, the experimental methods without specific conditions are usually in accordance with general conditions or in accordance with the manufacturer's recommendations. Unless otherwise specified, percentages and ratios are calculated by weight. EXAMPLES

[0412] The structural formulas of various isoquinoline compounds (berberine, berberine chloride, methylated coptisine, coptisine chloride, compound BBR-A1, compound BBR-A2 and compound BBR-A5) are as follows: [ka] JPEG0007616583000038.jpg166147JPEG0007616583000039.jpg91147

[0413] DNMT3a refers to DNA methyltransferase 3a, NCBI entrez gene:1788; Uniprotkb / Swiss-port:Q9Y6K1.

[0414] DNMT3b refers to DNA methyltransferase 3b, NCBI entrez gene:1789; Uniprotkb / Swiss-port:Q9UBC3.

[0415] DNMT1 refers to DNA methyltransferase 1, NCBI entrez gene:1786; Uniprotkb / Swiss-port:P26358.

[0416] UHRF1 refers to ubiquitin-related tau protein 1 containing PHD and RING finger domains, NCBI entrez gene:29128; Uniprotkb / Swiss-port:Q96T88.

[0417] The English name of the NNMT gene is Nicotinamide N-Methyltransferase.

[0418] The nucleotide sequence of the promoter region of the NNMT gene is shown in SEQ ID NO:1.

[0419] The region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site corresponds to positions 951 to 2500 of the nucleotide sequence shown in SEQ ID NO:1.

[0420] The region from 1050 bp before the transcription initiation site of the NNMT gene to 193 bp before the transcription initiation site corresponds to positions 951 to 1808 of the nucleotide sequence shown in SEQ ID NO:1.

[0421] The region from 840 bp before the transcription initiation site of the NNMT gene to 469 bp before the transcription initiation site corresponds to positions 1161 to 1532 of the nucleotide sequence shown in SEQ ID NO:1.

[0422] Example 1 Preparation of Compound 1 [ka]

[0423] Coptisine / berberine (12.0g, 35.6mmol) was added to a 100mL single-hole flask, and simultaneously vacuum was applied with an oil pump, and the reaction mixture was slowly heated to 190-210℃ for 2 hours, during which the solid turned from yellow to dark red. The reaction was monitored by TLC to determine the complete conversion of the raw material coptisine (DCM:MeOH=10:1). The crude reaction product was cooled to room temperature and purified by silica gel column chromatography (eluent DCM:MeOH=20:1) to obtain compound 1 (weight 8.2g, yield 79%) as a dark red powder.

[0424] compound 1 1 H NMR(400MHz,CD3OD):δ 9.26(s,1H),8.02 (s,1H),7.52(d,J=8.0Hz,1H),7.43(s,1H),6.88(d,J=8.0Hz,1H),6.83(s,1H),6.03 (s,2H),4.60(t,J=6.0Hz,2H),3.87(s,3H),3.35(t,J=6.0Hz,2H),3.14-3.11(m,2H).

[0425] Example 2 Preparation of compound BBR-A1 [ka]

[0426] Compound 1 (200 mg, 0.62 mmol) and 1-propyl bromide (305 mg, 2.48 mmol, 4.0 eq) are dissolved in DMF (3 mL) and heated to 80 °C while stirring for 12 h. The reaction is monitored until the conversion of the raw material compound 1 is complete by TLC (DCM:MeOH = 10:1). The crude reaction product obtained by distilling off the solvent under reduced pressure is purified by silica gel column chromatography (eluent DCM:MeOH = 20:1) to obtain compound BBR-A1 (124 mg, 55%) as a yellow solid.

[0427] Compound BBR-A1 1 H NMR(400MHz,CD3OD):δ 9.68(s,1H),8.70 (s,1H),8.10(d,J=8.0Hz,1H),8.00(d,J=8.0 Hz,1H),7.66(s,1H),6.96(s,1H),6.11(s,2H),4.94(t,J=6.0Hz,2H),4.37(t,J=6.0 Hz,2H),4.10(s,3H),3.25(t,J=8.0Hz,2H),1.97-1.93(m,2H),1.13(t,J=7.2Hz,3H). ESI-MS(m / z): Theoretical value C 22 H 22 NO4, [M] +364.4, Observed value: 364.0.

[0428] Example 3 Preparation of compound BBR-A2 [ka]

[0429] Compound 1 (200 mg, 0.62 mmol) and allyl bromide (300 mg, 2.48 mmol, 4.0 equiv) are dissolved in DMF (3 mL), heated to 80 °C and stirred for 12 h. The reaction is monitored until the conversion of raw material compound 1 is complete (DCM:MeOH = 10:1). The crude reaction product obtained by distilling off the solvent under reduced pressure is purified by silica gel column chromatography (eluent DCM:MeOH = 20:1) to obtain compound BBR-A2 (121 mg, 54%) as a yellow solid.

[0430] Compound BBR-A2 1 H NMR(400MHz,CD3OD):δ 9.72(s,1H),8.71(s,1H),8.11(d,J=8.0Hz,1H),8.01(d,J=8.0Hz,1H),7.67(s,1H),6.97(s,1H),6.26-6.19(m,1H) ),6.11(s,2H),5.44(d,J=16.0Hz,1H),5.28(d,J=16.0Hz,1H),4.96-4.84(m,4H),4.11(s,3H),3.28-3.24(m,2H). ESI-MS(m / z): Theoretical value C 22 H 20 NO4, [M] +362.4, Observed value: 362.0.

[0431] Example 4 Preparation of compound BBR-A5 [ka]

[0432] Compound 1 (200 mg, 0.62 mmol) and tert-butyl bromoacetate (484 mg, 2.48 mmol, 4.0 equiv) are dissolved in DMF (3 mL) and heated to 80 °C while stirring for 12 h. The reaction is monitored until the conversion of raw material compound 1 is complete (DCM:MeOH = 10:1). The crude reaction product obtained by distilling off the solvent under reduced pressure is purified by silica gel column chromatography (eluent DCM:MeOH = 20:1) to obtain compound BBR-A5 (175 mg, 65%) as a yellow solid.

[0433] Compound BBR-A5 1 H NMR(400MHz,CD3OD):δ 9.97(s,1H),8.71 (s,1H),8.12(d,J=8.0Hz,1H),8.00(d,J=8.0Hz,1H),7.67(s,1H),6.99(s,1H),6.11 (s,2H),5.03(s,2H),4.96-4.93(m,2H),4.10(s,3H),3.29-3.26(m,2H),1.46(s,9H). ESI-MS(m / z): Theoretical value C 25 H 26 NO6, [M] +436.5, Observed value: 436.0.

[0434] Example 5 The inhibitory effects of the isoquinoline compounds on various tumor cell lines are detected using cell activity detection agents.

[0435] Experimental background: Cell vitality was detected by Promega CellTiter-Glo kit, which directly measures intracellular ATP content and reflects cell activity. This experiment demonstrated the IC value of isoquinoline compounds that suppress the activity of various tumor cell lines. 50 Detect the value.

[0436] Experimental method and results: Various tumor cells were cultured in a medium containing 10% FBS (with P / S added). After subculture for 3 hours or overnight, various isoquinoline compounds were added in serial dilutions, and the median inhibitory concentration (IC) was determined after 3 days of culture. 50 The names, origins and culture conditions of each tumor cell line are as follows: cell line NCI-H82 (ATCC, no. HTB-175), cultured in RPMI1640 medium + P / S with 10% fetal bovine serum; cell line G-401 (ATCC, no. CRL-1441) cultured in McCoy's 5a medium + P / S with 10% fetal bovine serum; cell line MDA-MB-453 (ATCC, no. HTB-131) cultured in Leibovitz's L-15 medium + P / S with 10% fetal bovine serum; cell line SW48 (ATCC, no. CCL-231) cultured in Leibovitz's L-15 medium + P / S with 10% fetal bovine serum; cell line CFPAC-1 (ATCC, no. CRL-1918) cultured in IMDM medium + P / S with 10% fetal bovine serum; cell line 786-O (ATCC, no. CRL-1932) cultured in RPMI1640 medium + P / S with 10% fetal bovine serum; cell line GB-1 (JCRB, no. IFO50489), cultured in DMEM medium + P / S with 10% fetal bovine serum; Cell line SF126 (JCRB, number IFO50286) cultured in EMEM medium + P / S with 10% fetal bovine serum.

[0437] The experimental results are shown in Table 3 below. [Table 3] Note: IC 50 is the half inhibitory concentration (50% inhibiting concentration), i.e., the concentration of inhibitor at which 50% inhibitory effect is achieved.

[0438] As seen in Table 3, by detecting the sensitivity of various cells to isoquinoline compounds, NCI-H82 (human small cell lung cancer cells), G-401 (human renal cell carcinoma Wilms cells), MDA-MB-453 (breast cancer cells), and SW48 (human colon adenocarcinoma cells) showed high sensitivity to isoquinoline compounds (IC 50 GB-1 (human brain glioblastoma cells), CFPAC-1 (human pancreatic cancer cells), SF-126 (human brain tumor cells), and 786-O (renal clear cell adenocarcinoma cells) are sensitive to isoquinoline compounds (IC 50 They found that the α-amyloid ion concentration was insensitive to the α-amyloid ion concentration (high values).

[0439] Example 6 Gene expression analysis experiments were performed using RT-qPCR to detect the mRNA transcription levels of the NNMT gene in four tumor cell lines that were sensitive to isoquinoline compounds and four tumor cell lines that were insensitive to them, and to measure the NNMT gene expression patterns of these tumor cell lines, respectively. The experimental results are shown in Figure 1.

[0440] As can be seen from Figure 1, when performing gene expression analysis experiments using RT-qPCR to detect the mRNA transcription levels of the NNMT gene in four tumor cell lines sensitive to isoquinoline compounds (NCI-H82, G-401, MDA-MB-453, SW48) and four tumor cell lines insensitive to isoquinoline compounds (786-O, CFPAC-1, GB-1, and SF-126), it was found that the NNMT gene was low expressed in sensitive cells (NCI-H82, G-401, MDA-MB-453, and SW48) and high expressed in insensitive cells (786-O, CFPAC-1, GB-1, and SF-126).

[0441] Therefore, the conclusion that can be drawn from Figure 1 is that the inhibitory effect of isoquinoline compounds is significantly stronger on tumor cell lines with low NNMT gene expression than on tumor cell lines with high NNMT gene expression, that is, the expression of the NNMT gene in tumor cells is inversely correlated with the sensitivity to isoquinoline compounds.

[0442] Example 7 For the promoter region of the NNMT gene, the region from 1050bp before the transcription start site of the NNMT gene to 499bp after the transcription start site, and the region from 1050bp before the transcription start site of the NNMT gene to 193bp before the transcription start site of the NNMT gene in four tumor cell lines sensitive to isoquinoline compounds (NCI-H82, G-401, MDA-MB-453, and SW48) and four tumor cell lines insensitive to isoquinoline compounds (786-O, CFPAC-1, GB-1, and SF-126), sequencing was performed with bisulfite to detect the methylation level of DNA CpG sites in the relevant regions. Genomic DNA is treated with bisulfite, and unmethylated cytosines are deaminated to uracil, but methylated cytosines are not deaminated, so that methylation sites can be found by comparing the sequencing samples treated with bisulfite with the sequencing samples that were not treated. The experimental results are shown in Figures 2, 3, and 4.

[0443] As shown in Figure 2 (promoter region of the NNMT gene), Figure 3 (region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site), and Figure 4 (region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site), isoquinoline compounds have a strong inhibitory effect on tumor cells in which DNA CpG sites are hypermethylated in the promoter region of the NNMT gene, the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site, and the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site, but have a weak inhibitory effect on tumor cells in which DNA CpG sites are hypomethylated in the promoter region of the NNMT gene, the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site, and the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site. This indicates that the methylation levels of DNA CpG sites within the promoter region of the NNMT gene, the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site, and the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site in tumor cells are positively correlated with their sensitivity to isoquinoline compounds.

[0444] Example 8 In this study, we investigated the methylation of specific DNA CpG sites within the region from 840 bp before the transcription start site of the NNMT gene (position 114165695 on human chromosome 11) to 469 bp before the transcription start site (position 114166066 on human chromosome 11) in three tumor cell lines sensitive to isoquinoline compounds (NCI-H82, G-401, and SW48) and three tumor cell lines insensitive to isoquinoline compounds (786-O, CFPAC-1, and SF-126).

[0445] First, genomic DNA is treated with bisulfite, which deaminates unmethylated cytosines to uracil, but does not deaminate methylated cytosines, and by comparing the bisulfite-treated sequencing sample with the treated sequencing sample, methylation sites are found. Then, PCR amplification and sequencing analysis is performed on this region with primers to detect the methylation level of CpG sites within this DNA region.

[0446] Analysis revealed that seven CpG sites (positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050, and 114166066 on human chromosome 11) were almost all methylated in tumor cell lines sensitive to isoquinoline compounds (NCI-H82, G-401, and SW48), but none of these seven CpG sites were methylated in tumor cell lines insensitive to isoquinoline compounds (786-O, CFPAC-1, and SF-126). The methylation status of the relevant sites is shown in Figure 5.

[0447] The portions of the nucleotide sequence of SEQ ID NO:1 corresponding to positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050, and 114166066 on human chromosome 11 are shown below, respectively. [Table 4]

[0448] Example 9 The inhibitory effects of the isoquinoline compounds on various tumor cell lines are detected using cell activity detection agents.

[0449] Experimental background: Cell vitality was detected by Promega CellTiter-Glo kit, which directly measures intracellular ATP content and reflects cell activity. This experiment demonstrated the IC value of isoquinoline compounds that suppress the activity of various tumor cell lines. 50 Detect the value.

[0450] Experimental method and results: Various tumor cells were cultured in a medium containing 10% FBS (with P / S added). After subculture for 3 hours or overnight, various isoquinoline compounds were added in serial dilutions, and the median inhibitory concentration (IC) was determined after 3 days of culture. 50 The names, origins and culture conditions of each tumor cell line are as follows: cell line D341 Med (ATCC, no. HTB-187), cultured in EMEM medium + P / S with 20% fetal bovine serum; cell line Kelly (ECACC, no. 92110411) cultured in RPMI1640 medium + P / S with 10% fetal bovine serum and 2 mM glutamine; Cell line NB-1 (ATCC, no. HTB-131) cultured in Leibovitz's L-15 medium + P / S with 10% fetal bovine serum.

[0451] The experimental results are shown in Table 5 below. [Table 5] Note: IC 50 is the half inhibitory concentration (50% inhibiting concentration), i.e., the concentration of inhibitor at which 50% inhibitory effect is achieved.

[0452] As seen in Table 5, by detecting the sensitivity of various cells to isoquinoline compounds, D341 Med (cerebellar medulloblastoma), Kelly (neuroblastoma), and NB-1 (neuroblastoma) were found to be sensitive to isoquinoline compounds (IC 50 Although GB-1 (human brain glioblastoma cell line) and SF-126 (human brain tumor cell line) are sensitive to isoquinoline compounds (IC 50 They found that the α-amyloid ion concentration was insensitive to the α-amyloid ion concentration (high values).

[0453] Example 10 Gene expression analysis experiments were performed using RT-qPCR to detect the mRNA transcription levels of the NNMT gene in three tumor cell lines (D341 Med, Kelly, and NB-1) that are sensitive to isoquinoline compounds and two tumor cell lines (GB-1 and SF-126) that are insensitive to them, and to measure the NNMT gene expression patterns of these tumor cell lines. The experimental results are shown in Figure 6.

[0454] As can be seen from Figure 6, when gene expression analysis experiments were performed using RT-qPCR to detect the mRNA transcription levels of the NNMT gene in three tumor cell lines sensitive to isoquinoline compounds (D341 Med, Kelly, NB-1) and two tumor cell lines insensitive to them (GB-1, SF126), it was found that the NNMT gene was lowly expressed in the sensitive cells (D341 Med, Kelly, NB-1) and highly expressed in the insensitive cells (GB-1, SF126).

[0455] Therefore, the conclusion drawn from Figure 6 is that the inhibitory effect of isoquinoline compounds is significantly stronger on tumor cell lines with low NNMT gene expression than on tumor cell lines with high NNMT gene expression, i.e., the expression of the NNMT gene in tumor cells is inversely correlated with sensitivity to isoquinoline compounds.

[0456] Example 11 The promoter region of the NNMT gene, the region from 1050bp before the transcription start site of the NNMT gene to 499bp after the transcription start site, and the region from 1050bp before the transcription start site of the NNMT gene to 193bp before the transcription start site of the NNMT gene in three tumor cell lines (D341 Med, Kelly, and NB-1) that are sensitive to isoquinoline compounds and two tumor cell lines (GB-1, SF126) that are insensitive to isoquinoline compounds are sequenced with bisulfite to detect the methylation level of DNA CpG sites in the relevant regions. Genomic DNA is treated with bisulfite, and unmethylated cytosines are deaminated to uracil, but methylated cytosines are not deaminated, so that methylation sites are found by comparing the sequencing samples treated with bisulfite with the sequencing samples that were not treated. The experimental results are shown in Figures 7, 8, and 9.

[0457] As shown in Figure 7 (promoter region of the NNMT gene), Figure 8 (region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site), and Figure 9 (region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site), isoquinoline compounds have a strong inhibitory effect on tumor cells in which DNA CpG sites are hypermethylated in the promoter region of the NNMT gene, the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site, and the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site, but have a weak inhibitory effect on tumor cells in which DNA CpG sites are hypomethylated in the promoter region of the NNMT gene, the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site, and the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site. This indicates that the methylation levels of DNA CpG sites within the promoter region of the NNMT gene, the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site, and the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site in tumor cells are positively correlated with their sensitivity to isoquinoline compounds.

[0458] Example 12 The methylation level of cellular DNA is maintained by DNA methyltransferases DNMT3a, DNMT3b and DNMT1, and DNMT3a and DNMT3b perform de novo methylation on DNA, while DNMT1 replicates and maintains methylated DNA with the help of the protein UHRF1 (ubiquitin-like tau protein 1 containing PHD and RING finger domains). This example detects the correlation between NNMT expression in tumors and DNMT1, UHRF1, DNMT3a and DNMT3b expression.

[0459] Experimental method and results: Obtain the expression data of NNMT gene, DNMT1, UHRF1, DNMT3a and DNMT3b in various cells from the public database (Cancer Cell Line Encyclopedia, CCLE, a total of 1019 cell lines), then use bioinformatics methods to analyze the correlation between NNMT expression and DNMT1, UHRF1, DNMT3a and DNMT3b expression in these cells, and the correlation between the expression level of NNMT gene in each cell and the expression level of DNMT1, UHRF1, DNMT3a and DNMT3b. The experimental results are shown in Figure 10.

[0460] As can be seen from FIG. 10, the expression of NNMT in each cell is inversely correlated with the expression of DNA methyltransferase and UHRF1.

[0461] Example 13 The expression level of NNMT in the relevant cells is significantly inversely correlated with its sensitivity to isoquinoline compounds, whereas the expression level of its DNMT1 gene is significantly positively correlated with its sensitivity to isoquinoline compounds, further detecting the role of NNMT and DNMT1 in the sensitivity of cells to isoquinoline compounds.

[0462] Experimental method and results: NNMT gene is introduced into NCI-H82 cells via a viral vector to make NCI-H82 cells overexpress NNMT protein. After downregulating DNMT1 expression in NCI-H82 cells by shRNA introduction and detecting intracellular ATP to detect overexpression of NNMT protein and / or downregulation of DNMT1, the sensitivity of cells to isoquinoline compound (berberine chloride) is changed. The experimental results are shown in Figure 11. Vector is the control group of NCI-H82 cells introduced with empty virus.

[0463] As can be seen from FIG. 11, when NNMT protein (ov-NNMT in the figure) in NCI-H82 cells, which are sensitive to isoquinoline compounds, is solely overexpressed, or DNMT1 expression in NCI-H82 cells is downregulated using two different shRNAs targeting the DNMT1 gene (in the figure, sh-DNMT1 #1 is an shRNA targeting the DNMT1 gene, the corresponding DNA sequence is GATCCGGCCAATGAGACTGACATCAATT CAAGAGATTGATGTCAGTCTCATTGGGCTTTTTG (SEQ ID NO: 2); sh-DNMT1 #1 is another shRNA targeting the DNMT1 gene, the corresponding DNA sequence is GATCCGGATGAGTCCATCAAGGAAGATTCAAGAGATCTTCCTTGATGGACTCATCCTTTTTTG (SEQ ID NO: 3)), the NCI-H82 cells become less sensitive to berberine chloride. When NNMT protein was overexpressed in NCI-H82 cells while downregulating DNMT1 expression (ov-NNMT / sh-DNMT1 #1 and ov-NNMT / sh-DNMT1 #2 in the figure), the sensitivity of NCI-H82 cells to berberine chloride became more significantly reduced.

[0464] At the same time, the results of Western Blot experiment showed that the NNMT protein content of overexpressed NNMT protein in NCI-H82 (ov-NNMT) compared with normal NCI-H82 (Vector) is shown in Figure 12. The results of Western Blot experiment showed that the DNMT1 protein content of tumor cells down-regulated by both shRNAs in NCI-H82 (sh-DNMT1 #1 or sh-DNMT1 #2-DNMT1) compared with normal NCI-H82 (shVector) is shown in Figure 13.

[0465] Therefore, this embodiment further verifies that by overexpressing NNMT protein in NCI-H82 cells and downregulating DNMT1 expression in NCI-H82 cells, the NNMT expression level of tumor cells is significantly inversely correlated with its sensitivity to isoquinoline compounds, while the expression level of DNMT1 gene is significantly positively correlated with its sensitivity to inhibitors of the oxidative phosphorylation pathway.

[0466] Example 14 To verify whether cells sensitive to isoquinoline compounds still maintain sensitivity to isoquinoline compounds in vivo, berberine chloride is used to detect its effectiveness against mouse subcutaneous tumors inoculated with sensitive cells (NCI-H82).

[0467] Experimental method and results: 5x10 6 10 NCI-H82 cells and 5x10 cells in which NNMT protein was overexpressed and DNMT1 was underexpressed. 6 NCI-H82 cells (i.e. ov-NNMT / sh-DNMT1, the method of overexpressing NNMT protein and down-regulating the expression level of DNMT1 is mentioned in Example 13) are subcutaneously inoculated into nude mice to set up various tumor-bearing mice. Berberine chloride is intraperitoneally injected into the tumor-bearing mice of each group at a dosage of 10 mg / kg / day, and the changes in the tumor size of the mice over time are measured, and at the end of the experiment, the tumors of the mice of each group are dissected and photographed to detect the inhibitory effect of berberine chloride on these tumors. The control group is given the solvent by the same intraperitoneal injection. The tumor volume is calculated as follows: tumor volume = 1 / 2 length x width. 2 The experimental results are shown in Figures 14 and 15.

[0468] As can be seen from Figure 14 and Figure 15, berberine chloride significantly suppresses the subcutaneous tumor of nude mice inoculated with NCI-H82, but the inhibitory effect on the subcutaneous tumor of nude mice inoculated with ov-NNMT / sh-DNMT1 is lower than that on the subcutaneous tumor of nude mice inoculated with NCI-H82.This shows that isoquinoline compounds such as berberine chloride have a stronger inhibitory effect on tumors with low expression of NNMT, that is, tumors with low expression of NNMT have a strong sensitivity to isoquinoline compounds such as berberine chloride, and tumors with high expression of NNMT and low expression of DNMT1 have a weak sensitivity to isoquinoline compounds such as berberine chloride.

[0469] All documents cited above as references in this application are to be understood as being incorporated by reference. Moreover, it should be understood that after reading this text, those skilled in the art may make various modifications or alterations to the present invention, and equivalent forms thereof are also within the scope of the claims of this application.

Claims

1. Use of a compound of formula I, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, for the preparation of a composition or formulation for use in the prevention and / or treatment of tumors, comprising: wherein the tumor comprises a tumor in which the NNMT gene is underexpressed or not expressed; and / or The tumor comprises a tumor in which a nucleotide site in the NNMT gene is hypermethylated; and / or The tumor comprises a tumor in which NNMT gene region DNA CpG sites are hypermethylated; 【Chemistry 1】 Here, R １ , R ２ , R ３ , R ４ , R １０ , R １１ , R １２ and R １３ each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C12 alkyl group, a substituted or unsubstituted C3-C12 cycloalkyl group, a substituted or unsubstituted C1-C12 alkoxyl group, a substituted or unsubstituted C1-C12 alkylthiol group, a substituted or unsubstituted 3-12 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-12 membered heteroaryl group; or R １ and R ２ , R ２ and R ３ , R ３ and R ４ , R １０ and R １１ , R １１ and R １２ , and R １２ and R １３ each independently form a substituted or unsubstituted C3-C12 cycloalkyl ring, a substituted or unsubstituted 3-12 membered heterocycloalkyl ring, a substituted or unsubstituted C6-C12 aryl ring, or a substituted or unsubstituted 3-12 membered heteroaryl ring; R ５ , R ６ , R ７ , R ８ , R ９ and R １４ each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C12 alkyl group, a substituted or unsubstituted C3-C12 cycloalkyl group, a substituted or unsubstituted C1-C12 alkoxyl group, a substituted or unsubstituted C1-C12 alkylthiol group, a substituted or unsubstituted 3-12 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-12 membered heteroaryl group; Here, the optional "substitution" refers to one, two, three or four hydrogen atoms on the atomic group being replaced with a C1-C8 alkyl group, a C3-C8 cycloalkyl group, a C2-C4 alkenyl group, a C2-C4 alkynyl group, a C1-C8 halogenated alkyl group, a C3-C8 halogenated cycloalkyl group, a halogen atom, a nitro group, -CN, a carbonyl group, a cyano group, a hydroxyl group, a mercapto group, an amino group, a C1-C4 carboxyl group, a C2-C8 ester group, It refers to being substituted by a substituent selected from a C2-C4 acylamino group, a C1-C8 alkoxyl group, a C1-C8 alkylthiol group, a C3-C8 cycloalkoxyl group, a C3-C8 cycloalkylthiol group, a C1-C8 halogenated alkoxyl group, a C1-C8 halogenated alkylthiol group, a C6-C12 aryl group, a 5-10 membered heteroaryl group, a 5-10 membered heterocycloalkyl group, and a pyrrolidine-2,5-diketone group; The heterocycloalkyl group, heteroaryl group, heterocycloalkyl ring, and heteroaryl ring each independently have from 1 to 4 heteroatoms selected from N, O, and S on the heterocyclic ring.

2. The use according to claim 1 ,

2. R １ and R ４ each independently represents a hydrogen atom, a substituted or unsubstituted C1-C6 alkyl group, a substituted or unsubstituted C1-C6 alkoxyl group, or a substituted or unsubstituted C1-C6 alkylthiol group; R ２ and R ３ each independently represents a hydrogen atom, a substituted or unsubstituted C1-C6 alkyl group, a substituted or unsubstituted C1-C6 alkoxyl group, or a substituted or unsubstituted C1-C6 alkylthiol group; or R ２ and R ３ together form a substituted or unsubstituted 3-membered heterocycloalkyl ring, a substituted or unsubstituted 4-membered heterocycloalkyl ring, a substituted or unsubstituted 5-membered heterocycloalkyl ring, a substituted or unsubstituted 6-membered heterocycloalkyl ring, a substituted or unsubstituted 7-membered heterocycloalkyl ring, a substituted or unsubstituted 8-membered heterocycloalkyl ring, a substituted or unsubstituted 9-membered heterocycloalkyl ring, a substituted or unsubstituted 10-membered heterocycloalkyl ring, a substituted or unsubstituted 11-membered heterocycloalkyl ring, or a substituted or unsubstituted 12-membered heterocycloalkyl ring; R ５ , R ６ , R ７ , R ８ , R ９ and R １４ each independently represents a hydrogen atom, a halogen atom, -CN, a hydroxyl group, a mercapto group, a nitro group, an amino group, -COOH, -CHO, a substituted or unsubstituted C1-C8 alkyl group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C8 alkoxyl group, a substituted or unsubstituted C1-C8 alkylthiol group, a substituted or unsubstituted 3-10 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-10 membered heteroaryl group; R １０ , R １１ and R １２ are each independently a hydrogen atom or R １７ -A-; or R １０ and R １１ and R １１ and R １２ each independently form a substituted or unsubstituted 3-membered heterocycloalkyl ring, a substituted or unsubstituted 4-membered heterocycloalkyl ring, a substituted or unsubstituted 5-membered heterocycloalkyl ring, a substituted or unsubstituted 6-membered heterocycloalkyl ring, a substituted or unsubstituted 7-membered heterocycloalkyl ring, a substituted or unsubstituted 8-membered heterocycloalkyl ring, a substituted or unsubstituted 9-membered heterocycloalkyl ring, a substituted or unsubstituted 10-membered heterocycloalkyl ring, a substituted or unsubstituted 11-membered heterocycloalkyl ring, or a substituted or unsubstituted 12-membered heterocycloalkyl ring; where A is O or S; R １３ represents a hydrogen atom, a substituted or unsubstituted C1-C6 alkoxyl group, or a substituted or unsubstituted C1-C6 alkylthiol group; and / or R １７ represents a substituted or unsubstituted C1-C6 alkyl group, a C2-C4 alkenyl group-C1-C4 alkyl group-, a C2-C8 ester group-C1-C4 alkyl group-, a halogenated C1-C12 alkyl group-, a 5-7-membered heterocycloalkyl group-C1-C4 alkyl group-, a pyrrolidine-2,5-diketone group-C1-C4 alkyl group-, a cyano group-C1-C4 alkyl group-, a C1-C4 alkoxyl group-C2-C4 alkyl group-, a C2-C4 alkylthiol group-C1-C4 alkyl group-, or a 5-7-membered heteroaryl group-C1-C4 alkyl group- 2. The use according to claim 1 .

3. R １ represents a hydrogen atom; R ２ and R ３ are substituted or unsubstituted with each other. 【Chemistry 2】 Forming R ４ refers to a hydrogen atom; R ５ , R ６ , R ７ , R ８ and R ９ each independently represents a hydrogen atom, a methyl group, an ethyl group, a propyl group, or a butyl group; R １０ , R １１ and R １２ are each independently a hydrogen atom or R １７ -A-; or R １０ and R １１ , and R １１ and R １２ are each independently substituted or unsubstituted 【Chemistry 3】 Forming R １３ represents a hydrogen atom; R １４ represents a hydrogen atom, a methyl group, an ethyl group, a propyl group, or a butyl group; R １５ and R １６ each independently represents a hydrogen atom, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C3-C8 cycloalkyl group, a substituted or unsubstituted C1-C4 alkoxyl group, a substituted or unsubstituted C1-C4 alkylthiol group, a substituted or unsubstituted 3-8 membered heterocycloalkyl group, a substituted or unsubstituted C6-C12 aryl group, or a substituted or unsubstituted 3-8 membered heteroaryl group; R １７ represents a methyl group, an ethyl group, a propyl group, a butyl group, an amyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a vinyl group-methyl group-, an amyl ester group-methyl group-, a halogenated propyl group, a halogenated decyl group, a morpholinyl group-ethyl group-, a pyrrolidine-2,5-diketone group-ethyl group-, a cyano group-methyl group-, a methoxy group-ethyl group-, or a pyridine group-methyl group-; A stands for O or S; and / or W stands for O or S 2. The use according to claim 1 .

4. The structure of the compound of formula I is shown below in formula I-4: 【Chemistry 4】 where A is O or S; W is O or S; R １ , R ４ , R ５ , R ６ , R ７ , R ８ , R ９ , R １０ , R １１ , R １２ , R １３ and R １４ is as claimed in claim 1; Alternatively, the structure of the compound of formula I above is shown in formula I-5 below: 【Chemistry 5】 where A is O or S; W is O or S; R １ , R ４ , R ５ , R ６ , R ７ , R ８ , R ９ , R １０ , R １３ and R １４ is as claimed in claim 1; Alternatively, the structure of the compound of formula I above is shown in formula I-6: 【Chemistry 6】 where A is O or S; W is O or S; R １ , R ４ , R ５ , R ６ , R ７ , R ８ , R ９ , R １２ , R １３ and R １４ is as defined in claim 1 2. The use according to claim 1 .

5. The structure of the compound of formula I according to claim 1, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, is 【Chemistry 7】 【change】 2. The use according to claim 1 .

6. the tumor is a human tumor; the NNMT gene is a human NNMT gene; said expression includes protein expression and / or mRNA expression; the composition is a pharmaceutical composition; The composition or formulation further comprises a pharma- ceutically acceptable carrier; The composition or formulation is in solid, liquid or semi-solid form; and / or The composition or preparation is an oral preparation, an external preparation, or an injectable preparation.

2. The use according to claim 1 .

7. The tumor in which the NNMT gene is under-expressed or not expressed refers to a tumor in which the ratio (E1 / E0) between the expression level E1 of the NNMT gene in a tumor cell and the expression level E0 of the NNMT gene in the same cell or a normal cell is <1.0, and the same cell refers to a similar tumor cell in which the NNMT gene is normally expressed; A tumor in which the nucleotide site of the NNMT gene is hypermethylated refers to a tumor in which the ratio (L1 / L0) between the methylation level L1 of the nucleotide site of the NNMT gene in a tumor cell and the methylation level L0 of the nucleotide site of the NNMT gene in an identical cell or a normal cell is >1.0, and the identical cell refers to a similar tumor cell in which the nucleotide site of the NNMT gene is normally methylated; and / or The tumor in which the DNA CpG site of the NNMT gene region is hypermethylated refers to a tumor in which the ratio (W1 / W0) between the methylation level W1 of the DNA CpG site of the NNMT gene region in tumor cells and the methylation level W0 of the DNA CpG site of the NNMT gene region in the same cell or normal cell is >1.0, and the same cell refers to a similar tumor cell in which the DNA CpG site of the NNMT gene region is normally methylated.

2. The use according to claim 1 .

8. The tumor in which the NNMT gene is under-expressed or not expressed refers to a tumor in which the ratio (E1 / E0) between the expression level E1 of the NNMT gene in a tumor cell and the expression level E0 of the NNMT gene in the same cell or a normal cell is ≦0.7, and the same cell refers to a similar tumor cell in which the NNMT gene is normally expressed; A tumor in which the nucleotide site of the NNMT gene is hypermethylated refers to a tumor in which the ratio (L1 / L0) between the methylation level L1 of the nucleotide site of the NNMT gene in a tumor cell and the methylation level L0 of the nucleotide site of the NNMT gene in an identical cell or a normal cell is ≧2, and the identical cell refers to a similar tumor cell in which the nucleotide site of the NNMT gene is normally methylated; and / or The tumor in which the DNA CpG site of the NNMT gene region is hypermethylated refers to a tumor in which the ratio (W1 / W0) between the methylation level W1 of the DNA CpG site of the NNMT gene region in tumor cells and the methylation level W0 of the DNA CpG site of the NNMT gene region in the same cell or normal cell is ≧2, and the same cell refers to a similar tumor cell in which the DNA CpG site of the NNMT gene region is normally methylated.

2. The use according to claim 1 .

9. The tumor in which the NNMT gene is under-expressed or not expressed refers to a tumor in which the ratio (E1 / E0) between the expression level E1 of the NNMT gene in a tumor cell and the expression level E0 of the NNMT gene in the same cell or a normal cell is ≦0.4, and the same cell refers to a similar tumor cell in which the NNMT gene is normally expressed; A tumor in which the nucleotide site of the NNMT gene is hypermethylated refers to a tumor in which the ratio (L1 / L0) between the methylation level L1 of the nucleotide site of the NNMT gene in a tumor cell and the methylation level L0 of the nucleotide site of the NNMT gene in an identical cell or a normal cell is ≧5, and the identical cell refers to a similar tumor cell in which the nucleotide site of the NNMT gene is normally methylated; and / or The tumor in which the DNA CpG site of the NNMT gene region is hypermethylated refers to a tumor in which the ratio (W1 / W0) between the methylation level W1 of the DNA CpG site of the NNMT gene region in tumor cells and the methylation level W0 of the DNA CpG site of the NNMT gene region in the same cell or normal cell is ≧5, and the same cell refers to a similar tumor cell in which the DNA CpG site of the NNMT gene region is normally methylated.

2. The use according to claim 1 .

10. The tumor in which the NNMT gene is under-expressed or not expressed refers to a tumor in which the ratio (E1 / E0) between the expression level E1 of the NNMT gene in a tumor cell and the expression level E0 of the NNMT gene in the same cell or a normal cell is ≦0.1, and the same cell refers to a similar tumor cell in which the NNMT gene is normally expressed; A tumor in which the nucleotide site of the NNMT gene is hypermethylated refers to a tumor in which the ratio (L1 / L0) between the methylation level L1 of the nucleotide site of the NNMT gene in a tumor cell and the methylation level L0 of the nucleotide site of the NNMT gene in an identical cell or a normal cell is ≧10, and the identical cell refers to a similar tumor cell in which the nucleotide site of the NNMT gene is normally methylated; and / or The tumor in which the DNA CpG site of the NNMT gene region is hypermethylated refers to a tumor in which the ratio (W1 / W0) between the methylation level W1 of the DNA CpG site of the NNMT gene region in tumor cells and the methylation level W0 of the DNA CpG site of the NNMT gene region in the same cell or normal cell is ≧10, and the same cell refers to a similar tumor cell in which the DNA CpG site of the NNMT gene region is normally methylated.

2. The use according to claim 1 .

11. The tumor in which the nucleotide site of the NNMT gene is hypermethylated refers to a tumor in which the methylation level (M%) of the nucleotide site of the NNMT gene in tumor cells is ≧3% and ≦M1%, where M1 is any positive integer between 3 and 100; The methylation level of the nucleotide site of the NNMT gene refers to the ratio between the number of methylated nucleotides in the NNMT gene region and the number of all nucleotides in the NNMT gene region; The methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide site of the NNMT gene promoter region; The methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide site within the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site; The methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide site within the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site; The methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide site within the region from 840 bp before the transcription start site of the NNMT gene to 469 bp before the transcription start site; The methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide site within a region between any two of positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050, and 114166066 of human chromosome 11 (including these two positions themselves); The methylation level of the nucleotide site of the NNMT gene comprises a methylation level of a nucleotide at a site selected from position 114165695 of human chromosome 11, position 114165730 of human chromosome 11, position 114165769 of human chromosome 11, position 114165804 of human chromosome 11, position 114165938 of human chromosome 11, position 114166050 of human chromosome 11, position 114166066 of human chromosome 11, or a combination thereof; The methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide site within the region between any two of the sites of positions 1161, 1196, 1235, 1270, 1404, 1516, and 1532 of the nucleotide sequence of SEQ ID NO:1 (including these two positions themselves); The methylation level of the nucleotide site of the NNMT gene includes the methylation level of the nucleotide at one or more of the following sites of the nucleotide sequence of SEQ ID NO:1: 1161, 1196, 1235, 1270, 1404, 1516, and 1532; The tumor with hypermethylation of the DNA CpG site of the NNMT gene region refers to a tumor in which the methylation level (M%) of the DNA CpG site of the NNMT gene region in tumor cells is ≧3% and ≦M2%, where M2 is any positive integer between 3 and 100; The methylation level of the DNA CpG site of the NNMT gene region refers to the ratio between the number of methylated CpG nucleotides in the NNMT gene region and the number of all nucleotides in the NNMT gene region; The methylation level of the DNA CpG site of the NNMT gene region refers to the ratio between the number of methylated CpG nucleotides in the NNMT gene region and the number of all CpG nucleotides in the NNMT gene region; The methylation level of the DNA CpG site in the NNMT gene region includes the methylation level of the DNA CpG site in the NNMT gene promoter region; The methylation level of DNA CpG sites in the NNMT gene region includes the methylation level of DNA CpG sites in the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site; The methylation level of the DNA CpG site in the NNMT gene region includes the methylation level of the DNA CpG site in the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site; The methylation level of the DNA CpG site in the NNMT gene region includes the methylation level of the DNA CpG site in the region from 840 bp before the transcription start site of the NNMT gene to 469 bp before the transcription start site; The methylation level of the DNA CpG site in the NNMT gene region includes the methylation level of the DNA CpG site in the region between any two of positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050, and 114166066 of human chromosome 11 (including these two positions themselves); The methylation level of the NNMT gene region DNA CpG site comprises the methylation level of a site selected from position 114165695 of human chromosome 11, position 114165730 of human chromosome 11, position 114165769 of human chromosome 11, position 114165804 of human chromosome 11, position 114165938 of human chromosome 11, position 114166050 of human chromosome 11, position 114166066 of human chromosome 11, or a combination thereof; The methylation level of the DNA CpG site of the NNMT gene region includes the methylation level of the DNA CpG site within the region between any two of the following positions: 1161, 1196, 1235, 1270, 1404, 1516, and 1532 of the nucleotide sequence of SEQ ID NO: 1 (including these two positions themselves); and / or The methylation level of the DNA CpG site of the NNMT gene region includes the methylation level of the site selected from the site of SEQ ID NO: 1 at positions 1161, 1196, 1235, 1270, 1404, 1516, 1532, or a combination thereof.

2. The use according to claim 1 .

12. M1 is 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 80, 85, 90, 95 or 100; M2 is 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 80, 85, 90, 95 or 100; The nucleotide sequence of the NNMT gene promoter region is shown in SEQ ID NO:1; The region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site is from position 951 to position 2500 of the nucleotide sequence shown in SEQ ID NO:1; The region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site is from position 951 to position 1808 of the nucleotide sequence shown in SEQ ID NO:1; and / or The region from 840 bp before the transcription start site of the NNMT gene to 469 bp before the transcription start site corresponds to positions 1161 to 1532 of the nucleotide sequence shown in SEQ ID NO:

1.

12. The use according to claim 11 .

13. The tumor is selected from lung cancer, kidney cancer, breast cancer, colon cancer, lymphoma, leukemia, pancreatic cancer, brain cancer, liver cancer, prostate cancer, or a combination thereof.

2. The use according to claim 1 .

14. The lung cancer is selected from non-small cell lung cancer, small cell lung cancer, or a combination thereof; The colon cancer comprises colon adenocarcinoma; the lymphoma is selected from a B cell lymphoma, a T cell lymphoma, or a combination thereof; The brain tumor is selected from glioblastoma, glioma, medulloblastoma, neuroblastoma, or a combination thereof; The renal cancer is selected from renal clear cell adenocarcinoma, renal cancer Wilms, or a combination thereof; and / or The leukemia is selected from T-lymphocytic leukemia, myeloid leukemia, or a combination thereof.

14. The use according to claim 13.

15. The lymphoma comprises diffuse large B-cell lymphoma; The brain medulloblastoma comprises a cerebellar medulloblastoma; The glioblastoma comprises glioblastoma multiforme; the renal cancer cancer cells include renal cancer Wilms cells; The T-lymphocytic leukemia comprises acute T-lymphocytic leukemia; The myeloid leukemia comprises M4 AML acute myeloid leukemia; and / or The myeloid leukemia includes FAB M4 grade AML acute myeloid leukemia.

15. The use according to claim 14.

16. A method for helping to determine whether a compound of formula I according to claim 1, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, is suitable for the prophylaxis and / or treatment of a tumor patient, the method comprising: When low or no expression of the NNMT gene, hypermethylation of nucleotide sites of the NNMT gene, and / or hypermethylation of DNA CpG sites in the NNMT gene region are detected in tumor cells of a tumor patient compared to normal cells, it is determined that the compound of formula I according to claim 1, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, is suitable for the prevention and / or treatment of the tumor patient; When high expression of the NNMT gene, hypomethylation of nucleotide sites of the NNMT gene, and / or hypomethylation of DNA CpG sites in the NNMT gene region are detected in tumor cells of a tumor patient compared to normal cells, it is determined that the compound of formula I described in claim 1, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, is not suitable for the prevention and / or treatment of the tumor patient.

17. The tumor includes a tumor in which the NNMT gene is underexpressed or not expressed; the tumor comprises a tumor in which a nucleotide site in the NNMT gene is hypermethylated; The tumor comprises a tumor in which NNMT gene region DNA CpG sites are hypermethylated; The nucleotide site of the NNMT gene includes a nucleotide site of the NNMT gene promoter region; The nucleotide site of the NNMT gene includes the nucleotide site of the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site; The nucleotide site of the NNMT gene includes the nucleotide site of the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site; The nucleotide site of the NNMT gene includes the nucleotide site of the region from 840 bp before the transcription start site of the NNMT gene to 469 bp before the transcription start site; The nucleotide site of the NNMT gene includes a nucleotide site within a region between any two of positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050, and 114166066 of human chromosome 11 (including these two positions themselves); The nucleotide site of the NNMT gene comprises a site selected from position 114165695 on human chromosome 11, position 114165730 on human chromosome 11, position 114165769 on human chromosome 11, position 114165804 on human chromosome 11, position 114165938 on human chromosome 11, position 114166050 on human chromosome 11, position 114166066 on human chromosome 11, or a combination thereof; The nucleotide site of the NNMT gene includes a nucleotide site within a region between any two of positions 1161, 1196, 1235, 1270, 1404, 1516, and 1532 of the nucleotide sequence of SEQ ID NO:1 (including these two positions themselves); The nucleotide sites of the NNMT gene include one or more of the sites at positions 1161, 1196, 1235, 1270, 1404, 1516, and 1532 of the nucleotide sequence of SEQ ID NO:1; The NNMT gene region DNA CpG site includes a DNA CpG site in the NNMT gene promoter region; The DNA CpG site in the NNMT gene region includes the DNA CpG site in the region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site; The DNA CpG site in the NNMT gene region includes the DNA CpG site in the region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site; The DNA CpG site in the NNMT gene region includes the DNA CpG site in the region from 840 bp before the transcription start site of the NNMT gene to 469 bp before the transcription start site; The NNMT gene region DNA CpG site includes a DNA CpG site in the region between any two of positions 114165695, 114165730, 114165769, 114165804, 114165938, 114166050, and 114166066 of human chromosome 11 (including these two positions themselves); The NNMT gene region DNA CpG site comprises a site selected from position 114165695 on human chromosome 11, position 114165730 on human chromosome 11, position 114165769 on human chromosome 11, position 114165804 on human chromosome 11, position 114165938 on human chromosome 11, position 114166050 on human chromosome 11, position 114166066 on human chromosome 11, or a combination thereof; The NNMT gene region DNA CpG site comprises a DNA CpG site within the region between any two of positions 1161, 1196, 1235, 1270, 1404, 1516 and 1532 of the nucleotide sequence of SEQ ID NO:1 (including these two positions themselves); and / or The NNMT gene region DNA CpG site includes a site selected from the sites at positions 1161, 1196, 1235, 1270, 1404, 1516, 1532, or combinations thereof of SEQ ID NO:

1.

17. The method of claim 16.

18. The nucleotide sequence of the NNMT gene promoter region is shown in SEQ ID NO:1; The region from 1050 bp before the transcription start site of the NNMT gene to 499 bp after the transcription start site is from position 951 to position 2500 of the nucleotide sequence shown in SEQ ID NO:1; The region from 1050 bp before the transcription start site of the NNMT gene to 193 bp before the transcription start site is from position 951 to position 1808 of the nucleotide sequence shown in SEQ ID NO:1; and / or The region from 840 bp before the transcription start site of the NNMT gene to 469 bp before the transcription start site corresponds to positions 1161 to 1532 of the nucleotide sequence shown in SEQ ID NO:

1.

20. The method of claim 17 .

19. A method for producing a companion detection kit using the detection kit, comprising: The detection kit comprises: (i) a detection reagent used for detecting the expression level of the NNMT gene, the methylation level of a nucleotide site of the NNMT gene, and / or the methylation level of a DNA CpG site in the NNMT gene region; The said companion detection kit is used to determine whether the compound of formula I according to claim 1, or its optical isomer or racemate, or its solvate, or its pharma- ceutically acceptable salt, is suitable for the prophylaxis and / or treatment of tumor patients; The kit further comprises an instruction manual or label, the instruction manual or label including: When the NNMT gene is under-expressed or not expressed, the nucleotide site of the NNMT gene is hypermethylated, and / or the DNA CpG site of the NNMT gene region is hypermethylated in the tumor cells of a tumor patient, the compound of formula I according to claim 1, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, becomes suitable for the prevention and / or treatment of the tumor patient; and / or The disclosure states that when high expression of the NNMT gene, low methylation of the nucleotide site of the NNMT gene, and / or low methylation of the DNA CpG site in the NNMT gene region occurs in tumor cells of a tumor patient, the compound of formula I described in claim 1, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof becomes unsuitable for the prevention and / or treatment of the tumor patient. Method for producing the companion detection kit.

20. (i) a detection agent used to detect the expression level of the NNMT gene, the methylation level of a nucleotide site of the NNMT gene, and / or the methylation level of a DNA CpG site in the NNMT gene region; (ii) a compound of formula I according to claim 1, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof. A medical kit comprising:

21. (i) a detection module used to detect the expression level of the NNMT gene, the methylation level of the nucleotide site of the NNMT gene, and / or the methylation level of the DNA CpG site of the NNMT gene region; (ii) information that under- or non-expression of the NNMT gene, hypermethylation of nucleotide sites of the NNMT gene, and / or hypermethylation of DNA CpG sites in the NNMT gene region in tumor cells of a tumor patient renders the compound of formula I according to claim 1, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, suitable for the prevention and / or treatment of a tumor patient; and / or and an output module for outputting information that when high expression of the NNMT gene, low methylation of the nucleotide site of the NNMT gene, and / or low methylation of the DNA CpG site of the NNMT gene region occurs in tumor cells of a tumor patient, the compound of formula I according to claim 1, or an optical isomer or racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof becomes unsuitable for the prevention and / or treatment of the tumor patient. An apparatus or system comprising:

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