IP Library Granted Patent US 7,709,485
Granted Patent B2
US 7,709,485 · App. 11/869,055 · Granted May 4, 2010

IL-8 receptor antagonists

Assignee: GlaxoSmithkline LLC
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Quick Facts
Patent No.
US 7,709,485
App. No.
11/869,055
Granted
May 4, 2010
Kind
B2
Abstract

This invention relates to novel compounds of Formula (I) to (VII), and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).

Claims (12)

1. The compound N-[4-chloro-2-hydroxy-3-(1-piperazinylsulfonyl) phenyl]-N′-(2-chloro-3-fluorophenyl) urea, or a pharmaceutically acceptable salt thereof.

2. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier or diluent.

3. A method of treating a ELR chemokine mediated disease, wherein the chemokine binds to an IL-8 β (CXCR2) receptor in a human comprising administering to said human in need thereof an effective amount of a compound according to claim 1 , and wherein the disease is selected from the group consisting of asthma, chronic obstructive pulmonary disease and adult respiratory distress syndrome.

4. The method according to claim 3 wherein the disease is chronic obstructive pulmonary disease.

5. A method of treating a ELR chemokine mediated disease, wherein the chemokine binds to an IL-8 β (CXCR2) receptor in a human, comprising administering to said human in need thereof an effective amount of a compound according to claim 1 , and wherein the disease is selected from the group consisting of inflammatory bowel disease, Crohn's disease, or ulcerative colitis.

6. The method according to claim 5 wherein the disease is ulcerative colitis.

7. The method according to claim 5 wherein the disease is inflammatory bowel disease.

8. A method of treating a ELR chemokine mediated disease, wherein the chemokine binds to an IL-8 β (CXCR2) receptor in a human comprising administering to said human in need thereof an effective amount of a compound according to claim 1 , and wherein the disease is selected from the group consisting of psoriasis and atopic dermatitis.

9. The method according to claim 5 wherein the disease is psoriasis.

10. The compound according to claim 1 wherein the pharmaceutically acceptable salt is selected from the group consisting of hydrochloride, bromide, sulfate, phosphate, methane sulfonate, ethane sulfonate, acetate, malate, tartrate, citrate, lactate, oxalate, succinate, fumarate, maleate, benzoate, salicylate, phenylacetate, and mandelate.

11. The compound N-[4-chloro-2-hydroxy-3-(1-piperazinylsulfonyl)phenyl]-N′-(2-chloro-3-fluorophenyl) urea.

12. A pharmaceutical composition comprising a compound according to claim 11 and a pharmaceutically acceptable carrier or diluent.

Assignments (2)
CHANGE OF NAME Recorded Feb 3, 2010
From: SMITHKLINE BEECHAM CORPORATION
To: GLAXOSMITHKLINE LLC
Reel/Frame 023890/0563 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 12, 2008
From: BUSCH-PETERSEN, JAKOB; PALOVICH, MICHAEL R; WIDDOWSON, KATHERINE L
To: SMITHKLINE BEECHAM CORPORATION
Reel/Frame 021373/0957 →
Continuity (3)
Continuation 1053295600
Provisional Application 6042195600 · Oct 29, 2002
Related Publication 20090093492A1 · Apr 9, 2009