IP Library Granted Patent US 6,888,027
Granted Patent B2
US 6,888,027 · App. 10/381,790 · Granted May 3, 2005

Carbamic acid compounds comprising a sulfonamide linkage as HDAC inhibitors

Assignee: Topotarget UK Limited
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Quick Facts
Patent No.
US 6,888,027
App. No.
10/381,790
Granted
May 3, 2005
Kind
B2
Abstract

This invention pertains to certain active carbamic acid compounds which inhibit HDAC activity and which have the following formula: (I) A is an aryl group; Q 1 is a covalent bond or an aryl leader group; J is a sulfonamide linkage selected from: —S(═O) 2 NR 1 — and —NR 1 S(═O) 2 —; R1 is a sulfonamido substituent; and, Q 2 is an acid leader group; with the proviso that if J is —S(═O) 2 NR 1 —, then Q 1 is an aryl leader group; and pharmaceutically acceptable salts, solvates, amides, esters, ethers, chemically protected forms, and prodrugs thereof. The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit HDAC, and, e.g., to inhibit proliferative conditions, such as cancer and psoriasis.

Claims (140)

1. A compound of the formula:

wherein:

A is an unsubstituted phenyl group;

Q 1 is a covalent bond or a C 1-7 alkylene group;

J is:

R 1 is hydrogen, C 1-7 alkyl, C 3-20 heterocyclyl, or C 5-20 aryl; and,

Q 2 is:

and pharmaceutically acceptable salts thereof.

2. A compound according to claim 1 , wherein Q 1 is a covalent bond.

3. A compound according to claim 1 , wherein Q 1 is a C 1-7 alkylene group.

4. A compound according to claim 1 , wherein Q 1 is:

a saturated linear C 1-7 alkylene group,

a saturated branched C 1-7 alkylene group,

a partially unsaturated linear C 1-7 alkylene group, or

a partially unsaturated branched C 1-7 alkylene group.

5. A compound according to claim 1 , wherein Q 1 is —CH 2 —.

6. A compound according to claim 1 , wherein Q 1 is —CH(CH 3 )—.

7. A compound according to claim 1 , wherein Q 1 is —CH(CH 2 CH 3 )—.

8. A compound according to claim 1 , wherein Q 1 is —CH 2 CH 2 —.

9. A compound according to claim 1 , wherein Q 1 is —CH 2 CH(CH 3 )—.

10. A compound according to claim 1 , wherein Q 1 is —CH(CH 3 )CH 2 —.

11. A compound according to claim 1 , wherein Q 1 is —CH 2 CH(CH 2 CH 3 )—.

12. A compound according to claim 1 , wherein Q 1 is —CH(CH 2 CH 3 )CH 2 —.

13. A compound according to claim 1 , wherein Q 1 is —CH═CH—.

14. A compound according to claim 1 , wherein Q 1 is —CH 2 CH 2 CH 2 —.

15. A compound according to claim 1 , wherein Q 1 is —CH═CHCH 2 —.

16. A compound according to claim 1 , wherein Q 1 is —CH 2 CH 2 CH 2 CH 2 —.

17. A compound according to claim 1 , wherein Q 1 is —CH═CH 2 CH═CH—.

18. A compound according to claim 1 , wherein Q 1 is selected from:

—(CH 2 ) 2 —,

—CH(CH 3 )CH 2 —,

—CH 2 CH(CH 3 )—,

—CH(CH 2 CH 3 )CH 2 —,

—CH 2 CH(CH 2 CH 3 )—,

—CH═CH—;

—(CH 2 ) 3 —,

—CH(CH 3 )CH 2 CH 2 —,

—CH 2 CH(CH 3 )CH 2 —,

—CH 2 CH 2 CH(CH 3 )—,

—CH(CH 2 CH 3 )CH 2 CH 2 —,

—CH 2 CH(CH 2 CH 3 )CH 2 —,

—CH 2 CH 2 CH(CH 2 CH 3 )—,

—CH═CHCH 2 —,

—CH 2 CH═CH—,

—C(CH 3 )═CH—,

—CH═C(CH 3 )—,

—C(CH 3 )═CHCH 2 —,

—CH═C(CH 3 )CH 2 —,

—CH═CHCH(CH 3 )—,

—CH(CH 3 )CH═CH—,

—CH 2 C(CH 3 )═CH—,

—CH 2 CH═C(CH 3 )—;

—(CH 2 ) 4 —,

 —CH(CH 3 )CH 2 CH 2 CH 2 —,

—CH 2 CH(CH 3 )CH 2 CH 2 —,

—CH 2 CH 2 CH(CH 3 )CH 2 —,

—CH 2 CH 2 CH 2 CH(CH 3 )—,

—CH(CH 2 CH 3 )CH 2 CH 2 CH 2 —,

—CH 2 CH(CH 2 CH 3 )CH 2 CH 2 —,

—CH 2 CH 2 CH(CH 2 CH 3 )CH 2 —,

—CH 2 CH 2 CH 2 CH(CH 2 CH 3 )—,

—CH═CHCH 2 CH 2 —,

—CH 2 CH═CHCH 2 —,

—CH 2 CHCH═CH—,

—CH═CHCH═CH—;

—(CH 2 ) 5 —,

—CH(CH 3 )CH 2 CH 2 CH 2 CH 2 —,

—CH 2 CH(CH 3 )CH 2 CH 2 CH 2 —,

—CH 2 CH 2 CH(CH 3 )CH 2 CH 2 —,

—CH 2 CH 2 CH 2 CH(CH 3 )CH 2 —,

—CH 2 CH 2 CH 2 CH 2 CH(CH 3 )—,

—CH(CH 2 CH 3 )CH 2 CH 2 CH 2 CH 2 —,

—CH 2 CH(CH 2 CH 3 )CH 2 CH 2 CH 2 —,

—CH 2 CH 2 CH(CH 2 CH 3 )CH 2 CH 2 —,

—CH 2 CH 2 CH 2 CH(CH 2 CH 3 )CH 2 —,

—CH 2 CH 2 CH 2 CH 2 CH(CH 2 CH 3 )—,

—CH═CHCH 2 CH 2 CH 2 —,

—CH 2 CH═CHCH 2 CH 2 —,

—CH 2 CH 2 CH═CHCH 2 —,

—CH 2 CH 2 CH 2 CH═CH—,

—CH═CHCH═CHCH 2 —,

—CH 2 CH═CHCH═CH—,

—CH═CHCH 2 CH═CH—;

—(CH 2 ) 6 —,

—CH═CHCH 2 CH 2 CH 2 CH 2 —,

—CH 2 CH═CHCH 2 CH 2 CH 2 —,

—CH 2 CH 2 CH═CHCH 2 CH 2 —,

—CH 2 CH 2 CH 2 CH═CHCH 2 —,

—CH 2 CH 2 CH 2 CH 2 CH═CH—,

—CH═CHCH═CHCH 2 CH 2 —,

—CH═CHCH 2 CH═CHCH 2 —,

—CH═CHCH 2 CH 2 CH═CH—,

—CH 2 CH═CHCH═CHCH 2 —,

—CH 2 CH═CHCH 2 CH═CH—, and

—CH 2 CH 2 CH═CHCH═CH—.

19. A compound according to claim 1 , wherein R 1 is hydrogen.

20. A compound according to claim 2 , wherein R 1 is hydrogen.

21. A compound according to claim 3 , wherein R 1 is hydrogen.

22. A compound according to claim 4 , wherein R 1 is hydrogen.

23. A compound according to claim 5 , wherein R 1 is hydrogen.

24. A compound according to claim 6 , wherein R 1 is hydrogen.

25. A compound according to claim 7 , wherein R 1 is hydrogen.

26. A compound according to claim 8 , wherein R 1 is hydrogen.

27. A compound according to claim 9 , wherein R 1 is hydrogen.

28. A compound according to claim 10 , wherein R 1 is hydrogen.

29. A compound according to claim 11 , wherein R 1 is hydrogen.

30. A compound according to claim 12 , wherein R 1 is hydrogen.

31. A compound according to claim 13 , wherein R 1 is hydrogen.

32. A compound according to claim 14 , wherein R 1 is hydrogen.

33. A compound according to claim 15 , wherein R 1 is hydrogen.

34. A compound according to claim 16 , wherein R 1 is hydrogen.

35. A compound according to claim 17 , wherein R 1 is hydrogen.

36. A compound according to claim 18 , wherein R 1 is hydrogen.

37. A compound of the following formula, and pharmaceutically acceptable salts thereof:

38. A compound of the following formula, and pharmaceutically acceptable salts thereof:

39. A compound according to claim 1 , selected from compounds of the following formulae, and pharmaceutically acceptable salts and solvates thereof:

40. A composition comprising a compound according to claim 1 , and a pharmaceutically acceptable carrier.

41. A composition comprising a compound according to claim 37 , and a pharmaceutically acceptable carrier.

42. A composition comprising a compound according to claim 38 , and a pharmaceutically acceptable carrier.

43. A composition comprising a compound according to claim 39 , and a pharmaceutically acceptable carrier.

44. A method of inhibiting cell proliferation comprising contacting a cell with an effective amount of a compound according to claim 1 .

45. A method of inhibiting cell proliferation comprising contacting a cell with an effective amount of a compound according to claim 37 .

46. A method of inhibiting cell proliferation comprising contacting a cell with an effective amount of a compound according to claim 38 .

47. A method of inhibiting cell proliferation comprising contacting a cell with an effective amount of a compound according to claim 39 .

48. A method of inhibiting HDAC comprising contacting a cell with an effective amount of a compound according to claim 1 .

49. A method of inhibiting HDAC comprising contacting a cell with an effective amount of a compound according to claim 37 .

50. A method of inhibiting HDAC comprising contacting a cell with an effective amount of a compound according to claim 38 .

51. A method of inhibiting HDAC comprising contacting a cell with an effective amount of a compound according to claim 39 .

52. A method of treating a proliferative condition in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 1 .

53. A method of treating a proliferative condition in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 37 .

54. A method of treating a proliferative condition in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 38 .

55. A method of treating a proliferative condition in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 39 .

56. A method of treating cancer in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 1 .

57. A method of treating cancer in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 37 .

58. A method of treating cancer in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 38 .

59. A method of treating cancer in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 39 .

60. A method of treating psoriasis in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 1 .

61. A method of treating psoriasis in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 37 .

62. A method of treating psoriasis in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 38 .

63. A method of treating psoriasis in a patient comprising administering to said patient a therapeutically-effective amount of a compound according to claim 39 .

Assignments (4)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED ON REEL 046313 FRAME 0332. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jul 26, 2018
From: TOPOTARGET UK
To: SWK FUNDING LLC
Reel/Frame 046633/0664 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Jun 6, 2018
From: TOPOTARGET UK LIMITED
To: SWK FUNDING LLC
Reel/Frame 046313/0332 →
CHANGE OF ADDRESS Recorded Aug 22, 2013
From: TOPOTARGET UK LIMITED
To: TOPOTARGET UK LIMITED
Reel/Frame 031075/0707 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 20, 2004
From: WATKINS, CLARE J.; ROMERO-MARTIN, MARIA ROSARIO; MOORE, KATHRYN J.; RITCHIE, JAMES; FINN, PAUL W.; HARRIS, C. JOHN; DUFFY, JAMES E.S.; KALVINSH, IVARS; LOZA, EINARS; STARCHENKOV, IGOR; DIKOVSKA, KLARA; GAILITE, VIJA; VORONA, MAXIM; PISKUNOVA, IRINA; ANDRIANOV, VICTOR
To: TOPOTARGET UK LIMITED
Reel/Frame 015801/0031 →
Priority Claims (1)
GB 0023986 · Sep 29, 2000 · national
Continuity (3)
Provisional Application 6029778400 · Jun 14, 2001
Provisional Application 6030813600 · Jul 30, 2001
Related Publication 20040077726A1 · Apr 22, 2004