喹啉酮
药效团
数量结构-活动关系
化学
塞来昔布
药理学
立体化学
环氧合酶
卡拉胶
组合化学
酶
生物化学
医学
作者
Chaitanya Pr,G.D. Reddy,G. Varun,L.M. Srikanth,V.V.S.R. Prasad,A. Ravindernath
出处
期刊:Medicinal Chemistry
日期:2014-10-31
卷期号:10 (7): 711-723
被引量:9
标识
DOI:10.2174/1573406409666131128142843
摘要
A series of 36 novel substituted quinazolinone derivatives were synthesized and evaluated for their antiinflammatory activity by carrageenan induced paw inflammation model. The ability of these compounds to inhibit cyclooxygenase (COX-1 and 2) enzyme has been determined in-vitro; the results indicated that quinazolinone derivatives were selective towards COX-2 rather than COX-1. Among the quinazolinone derivatives tested, compound 32 showed better inhibition against COX-2 when compared with Celecoxib. Pharmacophore modeling and 3D QSAR studies were performed in order to elucidate structural insights for the anti-inflammatory activity.
科研通智能强力驱动
Strongly Powered by AbleSci AI