哌嗪
对接(动物)
吲哚试验
抗氧化剂
化学
组合化学
消炎药
立体化学
药理学
有机化学
医学
护理部
作者
T. Gul Altuntas,Aziz BAYDAR,Zühal Kılıç-Kurt,Cemre Acar,Sezen YILMAZ-SARIALTIN
标识
DOI:10.35333/jrp.2020.157
摘要
In this work, a series of piperazine substituted indole derivatives were synthesized and evaluated for their in vitro antioxidant and anti-inflammatory activities.The results of antioxidant activity showed that compounds 2 (81.63%) and 11 (85.63%) had comparable DPPH free radical scavenging activity to Vit E (88.6%).The in vitro antiinflammatory assays indicated that most of the compounds had more higher anti-inflammatory activities than standart ASA.Docking results revealed that compound 11 possessing the strongest anti-inflammatory activities showed the Hbond interactions with the key residues of COX-2 active site.It suggested that the anti-inflammatory activity of the compounds might result from COX-2 inhibition.It will be verified with further enzyme inhibition assays.
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