IP Library › Granted Patent US 10,988,476
Granted Patent B2
US 10,988,476 · App. 16/848,942 · Granted Apr 27, 2021

Substituted pyrimidines as cyclin-dependent kinase inhibitors

Inventors: Guangxin Xia (Shanghai, CN); Qian Wang (Shanghai, CN); Chen Shi (Shanghai, CN); Xiong Zhai (Shanghai, CN); Hui Ge (Shanghai, CN); Xuemei Liao (Shanghai, CN); Yu Mao (Shanghai, CN); Zhixiong Xiang (Shanghai, CN); Yanan Han (Shanghai, CN); Guoyong Huo (Shanghai, CN); Yanjun Liu (Shanghai, CN)
Assignee: SHANGHAI PHARMACEUTICALS HOLDING CO., LTD.
C07D471/04A61P35/00C07F5/025C07F7/083C07F7/0812C07F7/0816C07F9/6561C07F9/65842Y02P20/55
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Quick Facts
Patent No.
US 10,988,476
App. No.
16/848,942
Granted
Apr 27, 2021
Kind
B2
Abstract

The present invention discloses a substituted pyridine compound represented by formula I, and a pharmaceutically acceptable salt, stereoisomer and tautomer thereof. The compounds of the present invention are useful in the treatment of cancers.

Claims (46)

1. A compound represented by formula I:

or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof,

wherein:

m is 1;

n is 0;

p is 1;

q is 1;

R 1 is F;

R 2 is CH 3 ;

R 3 is CH(CH 3 ) 2 ;

R 4 is F;

R 5 is (CH 2 ) 2 N(R 11a )(R 11b );

R 6a is H;

R 6b is H;

R 6c is H;

R 6d is H;

R 11a is C 1 -C 3 alkyl;

R 11b is C 1 -C 3 alkyl;

X is N; and

Y is CH.

2. The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof, wherein R 11a is C 2 -C 3 alkyl.

3. The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof, wherein R 11a is CH 3 or CH 2 CH 3 .

4. The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof, wherein R 11b is C 2 -C 3 alkyl.

5. The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof, wherein R 11b is CH 3 or CH 2 CH 3 .

6. The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof, wherein:

R 11a is C 2 -C 3 alkyl; and

R 11b is C 2 -C 3 alkyl.

7. The compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof, wherein:

R 11a is CH 3 or CH 2 CH 3 ; and

R 11b is CH 3 or CH 2 CH 3 .

8. The compound according to claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt or tautomer thereof.

9. A pharmaceutical composition comprising at least one pharmaceutically acceptable excipient and a compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof.

10. A method for inhibiting cyclin-dependent kinase activity in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof.

11. A method for inhibiting tumor cells in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof.

12. The method according to claim 11 , wherein the tumor is selected from the group consisting of acute monocytic leukemia, brain astrocytoma, breast cancer, chronic myelogenous leukemia, colon cancer, gastric carcinoma, hepatocellular carcinoma, liver adenocarcinoma, malignant glioblastoma, non-small cell carcinoma, non-small cell lung cancer, pancreatic cancer, and prostate adenocarcinoma.

13. A method for treating a tumor in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the compound according to claim 1 , or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof.

14. The method according to claim 13 , wherein the tumor is selected from the group consisting of acute monocytic leukemia, brain astrocytoma, breast cancer, chronic myelogenous leukemia, colon cancer, gastric carcinoma, hepatocellular carcinoma, liver adenocarcinoma, malignant glioblastoma, non-small cell carcinoma, non-small cell lung cancer, pancreatic cancer, and prostate adenocarcinoma.

15. A compound selected from the group consisting of:

or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof.

16. A compound selected from the group consisting of:

or a pharmaceutically acceptable salt or tautomer thereof.

17. A compound selected from the group consisting of:

or a stereoisomer or tautomer thereof.

18. A compound selected from the group consisting of:

or a tautomer thereof.

Priority Claims (3)
CN 201511028799.6 · Dec 31, 2015 · national
CN 201610516637.5 · Jul 1, 2016 · national
CN 201610877404.8 · Sep 30, 2016 · national
Continuity (2)
Division 16067158
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