JNJ-7777120

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JNJ-7777120
Skeletal formula of JNJ-7777120
Ball-and-stick model of the JNJ-7777120 molecule
Systematic (IUPAC) name
5-chloro-2-[(4-methylpiperazin-1-yl)carbonyl]-1H-indole
Identifiers
CAS Number 459168-41-3 YesY
PubChem CID: 4908365
IUPHAR/BPS 1278
ChemSpider 4090750 N
ChEMBL CHEMBL129198 N
Synonyms 1-[(5-chloro-1H-indol-2-yl)carbonyl]-4-methylpiperazine
Chemical data
Formula C14H16ClN3O
Molecular mass 277.749 g/mol
  • C3CN(C)CCN3C(=O)c(cc1c2)nc1ccc2Cl
  • InChI=1S/C14H16ClN3O/c1-17-4-6-18(7-5-17)14(19)13-9-10-8-11(15)2-3-12(10)16-13/h2-3,8-9,16H,4-7H2,1H3 N
  • Key:HUQJRYMLJBBEDO-UHFFFAOYSA-N N
 NYesY (what is this?)  (verify)

JNJ-7777120 is a drug being developed by Johnson & Johnson Pharmaceutical Research & Development which acts as a potent and selective antagonist at the histamine H4 receptor.[1] It has anti-inflammatory effects,[2] and has been demonstrated to be superior to traditional antihistamines in the treatment of pruritus (itching).[3]

See also

References

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  1. Lua error in package.lua at line 80: module 'strict' not found.
  2. Thurmond RL, Desai PJ, Dunford PJ, Fung-Leung WP, Hofstra CL, Jiang W, Nguyen S, Riley JP, Sun S, Williams KN, Edwards JP, Karlsson L. A potent and selective histamine H4 receptor antagonist with anti-inflammatory properties. Journal of Pharmacology and Experimental Therapeutics. 2004 Apr;309(1):404-13. PMID 14722321
  3. Dunford PJ, Williams KN, Desai PJ, Karlsson L, McQueen D, Thurmond RL. Histamine H4 receptor antagonists are superior to traditional antihistamines in the attenuation of experimental pruritus. Journal of Allergy and Clinical Immunology. 2007 Jan;119(1):176-83. PMID 17208599