- JNJ 7777120
Drugbox
IUPAC_name = 1- [(5-chloro-1H-indol-2-yl)carbonyl] -4-methylpiperazine
CAS_number= 459168-41-3
ATC_prefix=
ATC_suffix=
PubChem= 4908365
DrugBank=
C=14 | H=16 | Cl=1 | N=3 | O=1
molecular_weight = 277.749 g/mol
smiles = C3CN(C)CCN3C(=O)c(cc1c2)nc1ccc2Cl
bioavailability=
metabolism =
elimination_half-life=
excretion =
pregnancy_category =
legal_status =
routes_of_administration=JNJ 7777120 is a drug being developed by
Johnson & Johnson Pharmaceutical Research & Development which acts as a potent and selective antagonist at thehistamine H4 receptor .cite journal |author=Jiang W, Lim HD, Zhang M, "et al" |title=Cloning and pharmacological characterization of the dog histamine H(4) receptor |journal=Eur. J. Pharmacol. |volume= |issue= |pages= |year=2008 |month=July |pmid=18639542 |doi=10.1016/j.ejphar.2008.06.095 |url=http://linkinghub.elsevier.com/retrieve/pii/S0014-2999(08)00709-7] It hasantiinflammatory effects, [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] and has been demonstrated to be superior to traditional antihistamines in the treatment ofpruritus (itching). [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]References
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