VUF-6002
 | |
| Systematic (IUPAC) name | |
|---|---|
|
(6-chloro-1H-benzimidazol-2-yl)-(4-methylpiperazin-1-yl)methanone | |
| Identifiers | |
| CAS Number |
869497-75-6  |
| PubChem | CID 10446295 |
| IUPHAR/BPS | 1277 |
| Chemical data | |
| Formula | C13H15ClN4O |
| Molar mass | 278.737 g/mol |
| |
| (verify) | |
VUF-6002 (JNJ-10191584) is a drug which acts as a potent and selective antagonist at the histamine H4 receptor.[1] It has antiinflammatory and analgesic effects in animal studies of acute inflammation.[2]
See also
References
- ↑ Zhang, M; Thurmond, RL; Dunford, PJ (2007). "The histamine H(4) receptor: a novel modulator of inflammatory and immune disorders". Pharmacology & therapeutics 113 (3): 594–606. doi:10.1016/j.pharmthera.2006.11.008. PMID 17275092.
- ↑ Coruzzi, G; Adami, M; Guaita, E; De Esch, IJ; Leurs, R (2007). "Antiinflammatory and antinociceptive effects of the selective histamine H4-receptor antagonists JNJ7777120 and VUF6002 in a rat model of carrageenan-induced acute inflammation". European Journal of Pharmacology 563 (1–3): 240–4. doi:10.1016/j.ejphar.2007.02.026. PMID 17382315.
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