IP Library Patent Application 12966516
Patent Application
App. No. 12/966,516

THIOTUNGSTATE ANALOGUES AND USES THEREOF

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Patent No.
US None
App. No.
12/966,516
Abstract

The current invention provides novel thiotungstate derivatives, methods of making novel thiotungstate derivatives, pharmaceutical compositions of novel thiotungstate derivatives, methods of using novel thiotungstate derivatives to treat diseases associated with aberrant vascularization, copper metabolism disorders and obesity and methods of using pharmaceutical compositions of thiotungstate derivatives to treat diseases associated with aberrant vascularization, copper metabolism disorders, neurodegenerative disorders, obesity or NF-κB dysregulation.

Claims (87)

1 . A compound of structural formula (I):

or a solvate or hydrate thereof wherein:

R 1 , R 2 , R 3 , R 5 , R 6 and R 7 are independently hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, cycloalkyl, substituted cycloalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, substituted heteroarylalkyl, heteroalkyl or substituted heteroalkyl;

R 4 and R 8 are independently hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, cycloalkyl, substituted cycloalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, substituted heteroarylalkyl, heteroalkyl or substituted heteroalkyl or are absent when N is part of an aromatic ring;

optionally, R 1 and R 2 taken together are alkyldiyl, substituted alkyldiyl, heteroalkyldiyl or substituted heteroalkyldiyl;

optionally, R 5 and R 6 taken together are alkyldiyl, substituted alkyldiyl, heteroalkyldiyl or substituted heteroalkyldiyl;

optionally, R 1 and R 2 taken together, R 2 and R 3 taken together and R 2 and R 4 taken together are alkyldiyl, substituted alkyldiyl, heteroalkyldiyl or substituted heteroalkyldiyl;

optionally, R 5 and R 6 taken together, R 6 and R 7 taken together and R 6 and R 8 taken together are alkyldiyl, substituted alkyldiyl, heteroalkyldiyl or substituted heteroalkyldiyl;

optionally, R 3 and R 7 taken together are alkyldiyl, substituted alkyldiyl, heteroalkyldiyl or substituted heteroalkyldiyl; and

Y −2 is (W 2 S 12 ) −2 , (W 2 S 9 ) −2 , (W 2 S 7 ) −2 , (W 2 S 8 ) −2 , (W 2 S 11 ) −2 , (W 2 S 6 ) −2 or (W 2 S 13 ) −2 .

2 . A compound of structural formula (I):

or a solvate or hydrate thereof wherein:

Y −2 is (WS 4 ) −2 ; and

a) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

wherein R 1 (R 2 )(R 3 )N has the structure:

b) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

wherein R 9 is n-C 8 H 17 , n-C 9 H 19 , n-C 10 H 21 , n-C 11 H 23 , n-C 12 H 25 , n-C 13 H 27 , n-C 14 H 29 , n-C 15 H 31 , n-C 16 H 33 , n-C 17 H 35 or n-C 18 H 37 ;

c) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

d) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

e) wherein R 1 (R 2 )(R 3 )N has the structure:

f) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

wherein R 5 , R 6 and R 7 are independently hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, cycloalkyl, substituted cycloalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, substituted heteroarylalkyl, heteroalkyl or substituted heteroalkyl;

R 8 is independently hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, cycloalkyl, substituted cycloalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, substituted heteroarylalkyl, heteroalkyl or substituted heteroalkyl or are absent when N is part of an aromatic ring;

optionally, R 5 and R 6 taken together are alkyldiyl, substituted alkyldiyl, heteroalkyldiyl or substituted heteroalkyldiyl; and

optionally, R 5 and R 6 taken together, R 6 and R 7 taken together and R 6 and R 8 taken together are alkyldiyl, substituted alkyldiyl, heteroalkyldiyl or substituted heteroalkyldiyl.

3 . The compound of claim 2 , wherein

a) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

wherein R 1 (R 2 )(R 3 )N has the structure:

b) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

wherein R 9 is n-C 8 H 17 , n-C 9 H 19 , n-C 10 H 21 , n-C 11 H 23 , n-C 12 H 25 , n-C 13 H 27 , n-C 14 H 29 , n-C 15 H 31 , n-C 16 H 33 , n-C 17 H 35 or n-C 18 H 37 ;

c) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

d) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

e) wherein R 1 (R 2 )(R 3 )N has the structure:

f) wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

4 . The compound of claim 2 , wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

wherein R 1 (R 2 )(R 3 )N has the structure:

5 . The compound of claim 2 , wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

wherein R 9 is n-C 8 H 17 , n-C 9 H 19 , n-C 10 H 21 , n-C 11 H 23 , n-C 12 H 25 , n-C 13 H 27 , n-C 14 H 29 , n-n-C 15 H 31 , n-C 16 H 33 , n-C 17 H 35 or n-C 18 H 37 .

6 . The compound of claim 2 , wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

7 . The compound of claim 2 , wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

8 . The compound of claim 2 , wherein R 1 (R 2 )(R 3 )N has the structure:

9 . The compound of claim 2 , wherein R 1 (R 2 )(R 3 )N has the structure:

10 - 35 . (canceled)

36 . A pharmaceutical composition comprising the compound of claim 2 and a pharmaceutically acceptable diluent, excipient or adjuvant.

37 . A method for treating cancer in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 2 .

38 . A method for treating cancer in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 36 .

39 . The method of claim 37 further comprising administering to the patient in need of such treatment a therapeutically effective amount of another anti-cancer agent or a pharmaceutical composition comprising i) said another anti-cancer agent and ii) a pharmaceutically acceptable diluent, excipient or adjuvant.

40 . The method of claim 38 further comprising administering to the patient in need of such treatment a therapeutically effective amount of another anti-cancer agent or a pharmaceutical composition comprising i) said another anti-cancer agent and ii) a pharmaceutically acceptable diluent, excipient or adjuvant.

41 . The method of claim 37 further comprising administering to the patient in need of such treatment a therapeutically effective amount of zinc or a pharmaceutical composition comprising i) zinc and ii) a pharmaceutically acceptable diluent, excipient or adjuvant.

42 . The method of claim 38 further comprising administering to the patient in need of such treatment a therapeutically effective amount of zinc or a pharmaceutical composition comprising i) zinc and ii) a pharmaceutically acceptable diluent, excipient or adjuvant.

43 . The method of claim 37 , wherein the cancer is breast cancer, renal cancer, brain cancer, colon cancer, prostrate cancer, chondrosarcoma or angiosarcoma.

44 . A method for treating wet type macular degeneration or rheumatoid arthritis in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 2 .

45 . A method for treating wet type macular degeneration or rheumatoid arthritis in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 36 .

46 . A method for treating aberrant vascularization in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 2 .

47 . A method for treating aberrant vascularization in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 36 .

48 . A method for treating excess copper levels in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 2 .

49 . A method for treating excess copper levels in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 36 .

50 . A method for treating obesity in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 2 .

51 . A method for treating obesity in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 36 .

52 . The method of claim 50 further comprising administering to the patient in need of such treatment a therapeutically effective amount of another anti-obesity agent or a pharmaceutical composition comprising i) said another anti-obesity agent and ii) a pharmaceutically acceptable diluent, excipient or adjuvant.

53 . The method of claim 51 further comprising administering to the patient in need of such treatment a therapeutically effective amount of another anti-obesity agent or a pharmaceutical composition comprising i) said another anti-obesity agent and ii) a pharmaceutically acceptable diluent, excipient or adjuvant.

54 . A method for treating neurodegenerative disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 2 .

55 . A method for treating neurodegenerative disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 36 .

56 . The method of claim 54 , wherein the neurodegenerative disease is Alzheimer's disease, amyotrophic lateral sclerosis or prion disease.

57 . The method of claim 55 , wherein the neurodegenerative disease is Alzheimer's disease, amyotrophic lateral sclerosis or prion disease.

58 . The method of claim 38 , wherein the cancer is breast cancer, renal cancer, brain cancer, colon cancer, prostrate cancer, chondrosarcoma or angiosarcoma.

59 . The compound of claim 6 , wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

and wherein R 1 (R 2 )(R 3 )(R 4 )N═R 5 (R 6 )(R 7 )(R 8 )N

60 . A pharmaceutical composition comprising the compound of claim 59 and a pharmaceutically acceptable diluent, excipient or adjuvant.

61 . The compound of claim 4 , wherein R 1 (R 2 )(R 3 )(R 4 )N═R 5 (R 6 )(R 7 )(R 8 )N or R 1 (R 2 )(R 3 )N═R 5 (R 6 )(R 7 )N.

62 . The compound of claim 5 , wherein R 1 (R 2 )(R 3 )(R 4 )N═R 5 (R 6 )(R 7 )(R 8 )N.

63 . The compound of claim 7 , wherein R 1 (R 2 )(R 3 )(R 4 )N has the structure:

and wherein R 1 (R 2 )(R 3 )(R 4 )N═R 5 (R 6 )(R 7 )(R 8 )N.

64 . The compound of claim 8 , wherein R 1 (R 2 )(R 3 )(R 4 )N═R 5 (R 6 )(R 7 )(R 8 )N.

65 . The compound of claim 9 , wherein R 1 (R 2 )(R 3 )(R 4 )N═R 5 (R 6 )(R 7 )(R 8 )N.

66 . A method for treating cancer in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 59 .

67 . The method of claim 66 further comprising administering to the patient in need of such treatment a therapeutically effective amount of another anti-cancer agent or a pharmaceutical composition comprising i) said another anti-cancer agent and ii) a pharmaceutically acceptable diluent, excipient or adjuvant.

68 . The method of claim 66 further comprising administering to the patient in need of such treatment a therapeutically effective amount of zinc or a pharmaceutical composition comprising i) zinc and ii) a pharmaceutically acceptable diluent, excipient or adjuvant.

69 . The method of claim 66 , wherein the cancer is breast cancer, renal cancer, brain cancer, colon cancer, prostrate cancer, chondrosarcoma or angiosarcoma.

70 . A method for treating wet type macular degeneration or rheumatoid arthritis in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 59 .

71 . A method for treating aberrant vascularization in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 59 .

72 . A method for treating excess copper levels in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 59 .

73 . A method for treating obesity in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 59 .

74 . The method of claim 73 further comprising administering to the patient in need of such treatment a therapeutically effective amount of another anti-obesity agent or a pharmaceutical composition comprising i) said another anti-obesity agent and ii) a pharmaceutically acceptable diluent, excipient or adjuvant.

75 . A method for treating neurodegenerative disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 59 .

76 . The method of claim 75 , wherein the neurodegenerative disease is Alzheimer's disease, amyotrophic lateral sclerosis or prion disease.

77 . A method for treating cancer, aberrant vascularization, wet type macular degeneration, rheumatoid arthritis, obesity or neurodegenerative disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 .

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2021
From: ALEXION PHARMA INTERNATIONAL OPERATIONS UNLIMITED COMPANY
To: ALEXION PHARMACEUTICALS, INC.
Reel/Frame 056837/0400 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2019
From: ALEXION BERMUDA PARTNERS, L.P.
To: ALEXION PHARMA INTERNATIONAL OPERATIONS UNLIMITED COMPANY
Reel/Frame 050947/0364 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2019
From: ALEXION BERMUDA L.P.
To: ALEXION BERMUDA PARTNERS, L.P.
Reel/Frame 050900/0736 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2019
From: WILSON THERAPEUTICS AB
To: ALEXION BERMUDA L.P.
Reel/Frame 050883/0053 →