Compound having Axl and c-Met kinase inhibitory activity, preparation thereof and application thereof
AssigneeShanghai Institute of Materia Medica, Chinese Academy of Sciences
InventorsWenhu Duan, Meiyu Geng, Hefeng Zhang, Jian Ding, Jing Ai, Xia Peng, Yinchun Ji
Life of this patent
Estimating the term…
Abstract
A compound having Axl and c-Met kinase inhibitory activity, a preparation method therefor and an application thereof are provided. Specifically, provided herein are a compound having the structure represented by formula (I), a preparation method therefor and an application thereof in the preparation of a medication for the treatment and/or prevention of tumor-associated diseases and/or kinase-related diseases.
Claims7
A compound of formula (I) or its stereoisomer, geometric isomer, tautomer, its pharmaceutically acceptable salt, its hydrate or solvate,
- wherein, T is selected from the group consisting of substituted or unsubstituted 5-10 membered aryl;
- the “substituted” means that one or more hydrogen atoms on the group is substituted by a substituent selected from the group consisting of unsubstituted C1-C6 alkyl, unsubstituted C3-C8 cycloalkyl, or halogen;
- U is selected from the group consisting of substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted C2-C6 alkenyl, substituted or unsubstituted C2-C6 alkynyl;
- the “substituted” means that one or more hydrogen atoms on the group is substituted by a substituent selected from the group consisting of unsubstituted C1-C6 alkoxy;
- Q is selected from N or C—Rc;
- V1, V2, V3 and V4 are the same or different, and are each independently C—Rd;
- Rc is H;
- Rd is selected from the group consisting of H, unsubstituted C1-C6 alkyl, or halogen;
- Z is formula (V):
- wherein R5a is at each occurrence independently selected from the group consisting of H, unsubstituted C1-C6 alkyl, unsubstituted C2-C6 alkenyl, or unsubstituted C2-C6 alkynyl;
- or the compound having formula (I) has formula (VI) or formula (VII):
- wherein R2a, R2b and R2c are at each occurrence independently selected from the group consisting of H, unsubstituted C1-C6 alkyl, unsubstituted C2-C6 alkenyl, unsubstituted C2-C6 alkynyl, unsubstituted-(CH2)t—(C3-C11 cycloalkyl), unsubstituted —(CH2)t-(3-11 membered heterocycloalkyl), and unsubstituted-(CH2)t—OR2d;
- R2d is H;
- W1, W2, W3, and W4 are at each occurrence independently selected from C—R1a;
- each R1a is H;
- each t is independently selected from 0, 1, 2, 3, or 4;
- or the compound having formula (I) has formula (XI) or formula (XII):
- wherein X1 is N or O;
- R4a is selected from the group consisting of H, halogen, and unsubstituted C1-C6 alkyl;
- Rg, Rh, Ri, Rj are at each occurrence independently H;
- for compound (XI), dotted line is a double bond;
- for compound (XII), dotted line is a single bond;
- M is C—H or N;
- Rk is at each occurrence independently selected from the group consisting of H, unsubstituted C1-C6 alkyl, unsubstituted C2-C6 alkenyl, or unsubstituted C2-C6 alkynyl.
A compound or its stereoisomer, geometric isomer, tautomer, its pharmaceutically acceptable salt, its hydrate or solvate, wherein, the compound is selected from the group consisting of:
- Compound
- Structural formula
- No. 1
- No. 2
- No. 3
- No. 4
- No. 5
- No. 7
- No. 10
- No. 11
- No. 14
- No. 15
- No. 17
- No. 19
- No. 25
- No. 26
- No. 28
- No. 29
- No. 38
- No. 41
- No. 42
- No. 51
Dependencies are inferred from the claim text.