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RU-2023128348-A - METHODS OF TREATMENT OF INFLAMMATION

RU2023128348ARU 2023128348 ARU2023128348 ARU 2023128348ARU-2023128348-A

Inventors

  • Стейнер, Митчелл С.
  • БАРНЕТ, Кестер Гари

Assignees

  • ВЕРУ ИНК.

Dates

Publication Date
20260508
Application Date
20210804
Priority Date
20210405

Claims (20)

  1. 1. A method of treating inflammation in a subject in need thereof by administering to the subject a composition containing a therapeutically effective amount of a compound of formula (I):
  2. wherein A is phenyl, indolyl or indazolyl optionally substituted with at least one of the following: (C 1 -C 4 ) alkyl, halo(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) haloalkyl, (C 1 -C 4 ) alkylamino, amino(C 1 -C 4 ) alkyl, F, Cl, Br, I, CN, -CH 2 CN, NH 2 , hydroxyl, OC(O)CF 3 , -OCH 2 Ph, -NHCO-(C 1 -C 4 ) alkyl, COOH, -C(O)Ph, C(O)O-(C 1 -C 4 ) alkyl, C(O)H, -C(O)NH 2 or NO 2 ;
  3. B is imidazole or benzimidazole optionally substituted with at least one of the following: (C 1 -C 4 ) alkyl, halo(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) alkyl, O-halo(C 1 -C 4 ) alkyl, F, Cl, Br, I, CN, -CH 2 CN, hydroxyl or NO 2 ;
  4. R 1 , R 2 and R 3 independently represent at least one of the following: hydrogen, (C 1 -C 4 ) alkyl, halo(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) haloalkyl, (C 1 -C 4 ) alkylamino, amino(C 1 -C 4 ) alkyl, F, Cl, Br, I, CN, -CH 2 CN, NH2, hydroxyl, OC(O)CF 3 , -OCH 2 Ph, -NHCO-(C 1 -C 4 ) alkyl, COOH, -C(O)Ph, C(O)O-(C 1 -C 4 ) alkyl, C(O)H, -C(O)NH 2 or NO 2 ;
  5. X represents a bond or NH;
  6. Y represents -C=O; and
  7. m is 1-3,
  8. or a pharmaceutically acceptable salt, hydrate, polymorph or isomer thereof.
  9. 2. The method of treating inflammation according to claim 1, wherein A is phenyl or indolyl optionally substituted with at least one of the following: (C 1 -C 4 ) alkyl, halo(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) haloalkyl, (C 1 -C 4 ) alkylamino, amino(C 1 -C 4 ) alkyl, F, Cl, Br, I, CN, -CH 2 CN, NH 2 , hydroxyl, OC(O)CF 3 , -OCH 2 Ph, -NHCO-(C 1 -C 4 ) alkyl, COOH, -C(O)Ph, C(O)O-(C 1 -C 4 ) alkyl, C(O)H, -C(O)NH 2 or NO 2 ;
  10. B is imidazole optionally substituted with at least one (C 1 -C 4 ) alkyl;
  11. R 1 , R 2 and R 3 independently represent at least one of the following: hydrogen, (C 1 -C 4 ) alkyl, halo(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) haloalkyl, (C 1 -C 4 ) alkylamino, amino(C 1 -C 4 ) alkyl, F, Cl, Br, I, CN, -CH 2 CN, NH2, hydroxyl, OC(O)CF 3 , -OCH 2 Ph, -NHCO-(C 1 -C 4 ) alkyl, COOH, -C(O)Ph, C(O)O-(C 1 -C 4 ) alkyl, C(O)H, -C(O)NH 2 or NO 2 ;
  12. X represents a bond or NH;
  13. Y represents -C=O; and
  14. m is 1-3,
  15. or a pharmaceutically acceptable salt, hydrate, polymorph or isomer thereof.
  16. 3. The method of treating inflammation according to claim 1, wherein A is phenyl optionally substituted with at least one of the following: (C 1 -C 4 ) alkyl, halo(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) haloalkyl, (C 1 -C 4 ) alkylamino, amino(C 1 -C 4 ) alkyl, F, Cl, Br, I, CN, -CH 2 CN, NH 2 , hydroxyl, OC(O)CF 3 , -OCH 2 Ph, -NHCO-(C 1 -C 4 ) alkyl, COOH, -C(O)Ph, C(O)O-(C 1 -C 4 ) alkyl, C(O)H, -C(O)NH 2 or NO 2 ;
  17. B is imidazole optionally substituted with at least one (C 1 -C 4 ) alkyl;
  18. R 1 , R 2 and R 3 independently represent at least one of the following: hydrogen, (C 1 -C 4 ) alkyl, halo(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) alkyl, O-(C 1 -C 4 ) haloalkyl, (C 1 -C 4 ) alkylamino, amino(C 1 -C 4 ) alkyl, F, Cl, Br, I, CN, -CH 2 CN, NH 2 , hydroxyl, OC(O)CF 3 , -OCH 2 Ph, -NHCO-(C 1 -C 4 ) alkyl, COOH, -C(O)Ph, C(O)O-(C 1 -C 4 ) alkyl, C(O)H, -C(O)NH 2 or NO 2 ;
  19. X represents a bond or NH;
  20. Y represents -C=O; and