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Volumn 20, Issue 12, 2010, Pages 3760-3763

Discovery of 4-{1-[({1-[4-(trifluoromethyl)benzyl]-1H-indol-7-yl}carbonyl) amino]cyclopropyl}benzoic acid (MF-766), a highly potent and selective EP 4 antagonist for treating inflammatory pain

Author keywords

EP4 antagonist; Inflammatory pain

Indexed keywords

4 [1 [[[1 [4 (TRIFLUOROMETHYL)BENZYL] 1H INDOL 7 YL]CARBONYL]AMINO]CYCLOPROPYL]BENZOIC ACID; MF 766; PROSTAGLANDIN RECEPTOR BLOCKING AGENT; UNCLASSIFIED DRUG;

EID: 77954213066     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2010.04.065     Document Type: Article
Times cited : (30)

References (20)
  • 12
    • 77954219318 scopus 로고    scopus 로고
    • note
    • Unpublished results: the elimination half-life of the corresponding sulfonamide M1 from MF-310 in rat and dog was estimated to be >24 h. When MF-310 was dosed orally at 20 mg/kg/day for 5 days in rats, M1 levels at 24 h increased from 1.4 μM after the first dose to 4.6 μM after the last dose. When it was dosed in dogs at 4 mg/kg/day for two weeks, M1 levels at 24 h increased from 1.3 μM after the first dose to 13.7 μM after the last dose.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.