IP Library Granted Patent US 10,137,120
Granted Patent B2
US 10,137,120 · App. 14/541,637 · Granted Nov 27, 2018

Aza-aryl 1H-pyrazol-1-yl benzene sulfonamides

Inventors: Xi Chen (E. Palo Alto, CA); Junfa Fan (Foster City, CA); Pingchen Fan (Fremont, CA); Antoni Krasinski (San Jose, CA); Lianfa Li (San Jose, CA); Rebecca M. Lui (Santa Clara, CA); Jeffrey P. McMahon (San Francisco, CA); Jay P. Powers (Pacifica, CA); Yibin Zeng (Foster City, CA); Penglie Zhang (Foster City, CA)
Assignee: ChemoCentryx, Inc.
A61K31/4709A61K31/415A61K31/4725A61K31/502A61K31/517A61K31/5377A61K45/06C07D231/42C07D401/04C07D401/06C07D401/10C07D403/04C07D403/10C07D405/14
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Quick Facts
Patent No.
US 10,137,120
App. No.
14/541,637
Granted
Nov 27, 2018
Kind
B2
Abstract

Compounds are provided that act as potent antagonists of the CCR(9) receptor. Animal testing demonstrates that these compounds are useful for treating inflammation, a hallmark disease for CCR(9). The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR(9)-mediated diseases, and as controls in assays for the identification of CCR(9) antagonists.

Claims (20)

1. A compound of the following formula:

2. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the compound of claim 1 .

3. A compound of the following formula:

or a pharmaceutically acceptable salt thereof.

4. The sodium salt of the compound of claim 3 .

5. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the compound or pharmaceutically acceptable salt thereof of claim 3 .

6. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the sodium salt of claim 4 .

7. A method for treating a CCR(9)-mediated disease or condition in a subject, the method comprising administering to the subject in need thereof a therapeutically-effective amount of a compound of claim 3 , wherein the CCR(9)-mediated disease or condition is selected from the group consisting of ulcerative colitis, Crohn's disease, inflammatory bowel disease, asthma, graft rejection, immune mediated food allergies, celiac disease, primary sclerosing cholangitis, and graft-v-host disease.

8. The method according to claim 7 , wherein the CCR(9)-mediated disease or condition is ulcerative colitis.

9. The method according to claim 7 , wherein the CCR(9)-mediated disease or condition is Crohn's disease.

10. The method according to claim 7 , wherein the CCR(9)-mediated disease or condition is primary sclerosing cholangitis.

11. The method according to claim 10 , wherein the primary sclerosing cholangitis is subsequent to or associated with an inflammatory bowel disease.

12. The method according to claim 7 , wherein the subject is a human.

13. The method according to claim 7 , where the administering is oral, parenteral, rectal, transdermal, sublingual, nasal or topical.

14. The method according to claim 7 , further comprising administering an anti-inflammatory or analgesic agent.

15. The method according to claim 14 , wherein the anti-inflammatory or analgesic agent is selected from the group consisting of an opiate agonist, lipoxygenase inhibitor, cyclooxygenase inhibitor, interleukin inhibitor, NMDA antagonist, inhibitor of nitric oxide or inhibitor of nitric oxide synthesis, aminosalicylates, corticosteroids or other immunosuppressive drugs, non-steroidal antiinflammatory agent, cytokine-suppressing antiinflammatory agent, biological TNF sequestrant, biological agents which target α4β7, ACE2 inhibitors, protein kinase C inhibitors, and a steroidal analgesic.

16. The method according to claim 14 , wherein the anti-inflammatory or analgesic agent is an 5-lipoxygenase inhibitor, cyclooxygenase-2 inhibitor, interleukin-1 inhibitor, HMG-CoA reductase inhibitor, or β2-agonist.

17. The method according to claim 14 , wherein the anti-inflammatory or analgesic agent is acetaminophen, aspirin, codeine, fentanyl, ibuprofen, indomethacin, ketorolac, morphine, naproxen, phenacetin, piroxicam, sufentanyl, sunlindac, or tenidap.

18. The method according to claim 7 , further comprising administering a compound selected from the group consisting of a pain reliever, potentiator, H2-antagonist, decongestant, antitussive, diuretic, sedating or non-sedating antihistamine, very late antigen (VLA-4) antagonist, immunosuppressant, EDG receptor agonist, steroid, non-steroidal anti-asthmatic agent, leukotriene antagonist, leukotriene biosynthesis inhibitor, inhibitor of phosphodiesterase type IV (PDE-IV), cholesterol lowering agent, sequestrant, cholesterol absorption inhibitor, anti-diabetic agent, α-glucosidase inhibitor, a β2-agonist, an HMG-CoA reductase inhibitor and glitazone.

19. The method according to claim 18 , wherein the compound is caffeine, simethicone, aluminum or magnesium hydroxide, pseudophedrine, codeine, cyclosporine, tacrolimus, rapamycin, FK-506, or insulin.

Assignments (2)
ASSIGNEE CHANGE OF ADDRESS Recorded Jun 27, 2023
From: CHEMOCENTRYX, INC.
To: CHEMOCENTRYX, INC.
Reel/Frame 064144/0685 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2018
From: CHEN, XI; FAN, JUNFA; FAN, PINGCHEN; KRASINSKI, ANTONI; LUI, REBECCA M.; MCMAHON, JEFFREY P.; POWERS, JAY P.; ZENG, YIBIN; ZHANG, PENGLIE; LI, LIANFA
To: CHEMOCENTRYX, INC.
Reel/Frame 044686/0962 →
Continuity (3)
Continuation 13781412 · Feb 28, 2013
Provisional Application 61604998 · Feb 29, 2012
Related Publication 20150073017A1 · Mar 12, 2015
Cited By (1)
US 12,611,404