IP Library Granted Patent US 8,785,433
Granted Patent B2
US 8,785,433 · App. 14/103,968 · Granted Jul 22, 2014

Quinoline derivatives as PI3 kinase inhibitors

Inventors: Steven David Knight (Collegeville, PA); Stanley J. Schmidt (Collegeville, PA)
Assignee: GlaxoSmithKline LLC
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Quick Facts
Patent No.
US 8,785,433
App. No.
14/103,968
Granted
Jul 22, 2014
Kind
B2
Abstract

Invented is a method of inhibiting the activity/function of PI3 kinases using quinoline derivatives. Also invented is a method of treating one or more disease states selected from: autoimmune disorders, inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, allergy, asthma, pancreatitis, multiorgan failure, kidney diseases, platelet aggregation, cancer, sperm motility, transplantation rejection, graft rejection and lung injuries by the administration of quinoline derivatives.

Claims (9)

1. A method of treating an autoimmune disease or an inflammatory disease comprising administering to a human in need thereof a therapeutically effective amount of 2,4-difluoro-N-{2-(methyloxy)-5-[4-(4-pyridazinyl)-6-quinolinyl]-3-pyridinyl}benzenesulfonamide, or a pharmaceutically acceptable salt thereof.

2. A method of treating an autoimmune disease or an inflammatory disease comprising administering to a human in need thereof a therapeutically effective amount of a pharmaceutical composition comprising 2,4-difluoro-N-{2-(methyloxy)-5-[4-(4-pyridazinyl)-6-quinolinyl]-3-pyridinyl}benzenesulfonamide, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

3. A method of treating an autoimmune disease or an inflammatory disease comprising administering to a human in need thereof a therapeutically effective amount of 2,4-difluoro-N-{2-(methyloxy)-5-[4-(4-pyridazinyl)-6-quinolinyl]-3-pyridinyl}benzenesulfonamide.

4. The method of claim 1 wherein the autoimmune disease or inflammatory disease is selected from a group consisting of multiple sclerosis, psoriasis, rheumatoid arthritis, systemic lupus erythematosis, inflammatory bowel disease, lung inflammation, thrombosis or brain infection/inflammation comprising meningitis and encephalitis.

5. The method of claim 2 wherein the autoimmune disease or inflammatory disease is selected from a group consisting of multiple sclerosis, psoriasis, rheumatoid arthritis, systemic lupus erythematosis, inflammatory bowel disease, lung inflammation, thrombosis or brain infection/inflammation comprising meningitis and encephalitis.

6. The method of claim 3 wherein the autoimmune disease or inflammatory disease is selected from a group consisting of multiple sclerosis, psoriasis, rheumatoid arthritis, systemic lupus erythematosis, inflammatory bowel disease, lung inflammation, thrombosis or brain infection/inflammation comprising meningitis and encephalitis.

7. The method of claim 1 wherein the autoimmune disease or inflammatory disease is psoriasis.

8. The method of claim 2 wherein the autoimmune disease or inflammatory disease is psoriasis.

9. The method of claim 3 wherein the autoimmune disease or inflammatory disease is psoriasis.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 12, 2013
From: ADAMS, NICHOLAS D.; BURGESS, JOELLE LORRAINE; DARCY, MICHAEL GERARD; DONATELLI, CARLA A.; KNIGHT, STEVEN DAVID; NEWLANDER, KENNETH ALLEN; RIDGERS, LANCE; SARPONG, MARTHA A.; SCHMIDT, STANLEY J.
To: SMITHKLINE BEECHAM CORPORATION
Reel/Frame 031768/0771 →
CHANGE OF NAME Recorded Dec 12, 2013
From: SMITHKLINE BEECHAM CORPORATION
To: GLAXOSMITHKLINE LLC
Reel/Frame 031804/0395 →
Continuity (4)
Continuation 13411887 · Mar 5, 2012
Division 12121891 · May 16, 2008
Provisional Application 60938761 · May 18, 2007
Related Publication 20140100234A1 · Apr 10, 2014