IP Library Granted Patent US 10,047,066
Granted Patent B2
US 10,047,066 · App. 12/744,860 · Granted Aug 14, 2018

IDO inhibitors

Inventors: Mario Mautino (Ames, IA); Firoz Jaipuri (Ames, IA); Agnieszka Marcinowicz-Flick (Ames, IA); Tanay Kesharwani (Ames, IA); Jesse Waldo (Ames, IA)
Assignee: NEWLINK GENETICS CORPORATION
C07D333/56A61K31/138A61K31/506C07C259/06C07C311/48C07C327/44C07C327/48C07C333/20C07D209/14C07D209/18C07D213/40C07D215/26C07D253/07C07D261/20C07D263/22C07D277/36C07D277/64C07D279/06C07D307/80C07D307/81C07D333/58C07D333/60C07D335/06C07D401/06C07D405/12C07D409/12C07D417/06C07D417/12
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Quick Facts
Patent No.
US 10,047,066
App. No.
12/744,860
Granted
Aug 14, 2018
Kind
B2
Abstract

Presently provided are methods for (a) modulating an activity of indoleamine 2,3-dioxygenase comprising contacting an indoleamine 2,3-dioxygenase with a modulation effective amount of a compound as described in one of the aspects described herein; (b) treating indoleamine 2,3-dioxygenase (IDO) mediated immunosuppression in a subject in need thereof, comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount of a compound as described in one of the aspects described herein; (c) treating a medical conditions that benefit from the inhibition of enzymatic activity of indoleamine-2,3-dioxygenase comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount of a compound as described in one of the aspects described herein; (d) enhancing the effectiveness of an anti-cancer treatment comprising administering an anti-cancer agent and a compound as described in one of the aspects described herein; (e) treating tumor-specific immunosuppression associated with cancer comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount of a compound as described in one of the aspects described herein; and (f) treating immunosuppression associated with an infectious disease, e.g., HIV-I infection, comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount a compound as described in one of the aspects described herein.

Claims (40)

1. A solid pharmaceutical composition comprising a pharmaceutically acceptable excipient, diluent, or carrier and a compound selected from the group consisting of:

O-((4,4′-dichlorobiphenyl-2-yl)methyl)hydroxylamine;

O-(5-chloro-2-(thiophen-3-yl)benzyl)hydroxylamine;

O-((4′-chlorobiphenyl-2-yl)methyl)hydroxylamine;

O-(5-chloro-2-(thiophen-2-yl)benzyl)hydroxylamine;

methyl 4-(aminooxy)-4-phenylbutanoate;

O-((4′-chlorobiphenyl-3-yl)methyl)hydroxylamine;

O-((3′,4,4′-trichlorobiphenyl-2-yl)methyl)hydroxylamine;

O-(5-chloro-2-(pyrimidin-5-yl)benzyl)hydroxylamine;

O-(5-chloro-2-(1H-indol-5-yl)benzyl)hydroxylamine;

(S)-2-(aminooxy)-N-methyl-2-phenylacetamide;

methyl 2-(aminooxy)-2-phenylacetate;

O-(1,3-diphenylpropyl)hydroxylamine;

3-(aminooxymethyl)-N-phenylaniline;

O-((4′,5-dichlorobiphenyl-3-yl)methyl)hydroxylamine;

2-(aminooxymethyl)-N-benzylaniline;

O-(3-cyclohexyl-1-phenylpropyl)hydroxylamine;

2-(aminooxymethyl)-N-phenylaniline;

O-(cyclohexyl(phenyl)methyl)hydroxylamine;

2-(aminooxy)-N-methyl-2-phenylacetamide;

O-(1,2-diphenylethyl)hydroxylamine;

O-(1,2,3,4-tetrahydronaphthalen-1-yl)hydroxylamine;

3-(aminooxymethyl)-N-benzylaniline;

O-(2-(pyridin-4-yl)benzyl)hydroxylamine;

O-(3-(pyridin-4-yl)benzyl)hydroxylamine;

O-(2-cyclohexyl-1-phenylethyl)hydroxylamine;

4-(aminooxy)-N-methyl-4-phenylbutanamide;

2-(aminooxy)-2-phenylethanamine;

3-(aminooxy)-3-phenylpropan-1-amine;

O-(2-morpholino-1-phenylethyl)hydroxylamine;

3-(aminooxymethyl)-N-benzylaniline;

2-(aminooxy)-N-methyl-2-phenylethanamine;

4-(aminooxy)-N-cyclohexyl-4-phenylbutanamide;

tert-butyl 2-(aminooxy)-2-phenylethylcarbamate;

(R)-2-(aminooxy)-N-methyl-2-phenylacetamide;

3-(aminooxy)-N-methyl-3-phenylpropan-1-amine;

N-(2-(aminooxy)-2-phenylethyl)acetamide;

O-(3-morpholino-1-phenylpropyl)hydroxylamine; and

(S)-3-(aminooxy)-3-phenylpropan-1-ol;

or a pharmaceutically acceptable salt thereof.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF THE ASSIGNEE NEWLINK GENETICS PREVIOUSLY RECORDED ON REEL 024715 FRAME 0534. ASSIGNOR(S) HEREBY CONFIRMS THE CORRECT ASSIGNEE NAME IS NEWLINK GENETICS CORPORATION. Recorded Apr 27, 2011
From: MAUTINO, MARIO R.; JAIPURI, FIROZ; MARCINOWICZ-FLICK, AGNIESZKA; KESHARWANI, TANAY; WALDO, JESSE; COLLIER, STEVEN JAMES
To: NEWLINK GENETICS CORPORATION
Reel/Frame 026189/0001 →
CORRECTIVE ASSIGNMENT TO CORRECT THE SPELLING OF INVENTOR'S NAME FIROZ JAIPURI PREVIOUSLY RECORDED ON REEL 024693 FRAME 0457. ASSIGNOR(S) HEREBY CONFIRMS THE CORRECT SPELLING OF INVENTOR'S NAME IS "FIROZ JAIPURI". Recorded Jul 20, 2010
From: MAUTINO, MARIO; JAIPURI, FIROZ; MARCINOWICZ-FLICK, AGNIESZKA; KESHARWANI, TANAY; WALDO, JESSE; COLLIER, STEVEN JAMES
To: NEWLINK GENETICS
Reel/Frame 024715/0534 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 15, 2010
From: MAUTINO, MARIO; JAIPURT, FIROZ; MARCINOWICZ-FLICK, AGNIESZKA; KESHARWANI, TANAY; WALDO, JESSE; COLLIER, STEVEN JAMES
To: NEWLINK GENETICS
Reel/Frame 024693/0457 →
Continuity (3)
Provisional Application 61050646 · May 6, 2008
Provisional Application 60991518 · Nov 30, 2007
Related Publication 20110053941A1 · Mar 3, 2011