查尔酮
白藜芦醇
赫拉
化学
哌嗪
细胞毒性T细胞
细胞凋亡
MTT法
体外
部分
细胞培养
细胞毒性
细胞生长
A549电池
活力测定
脂多糖
立体化学
药理学
生物化学
生物
免疫学
有机化学
遗传学
作者
Yu‐Lu Ma,Xi Zheng,Ping Zhu,Bei Liu,Hui Gao,Zewei Mao,Shouxin Zhang,Chunping Wan
出处
期刊:Mini-reviews in Medicinal Chemistry
[Bentham Science]
日期:2019-02-21
卷期号:19 (5): 424-436
被引量:5
标识
DOI:10.2174/1389557518666180727165358
摘要
Resveratrol and chalcones are lead compounds with good biological activities.In this study, a series of novel derivatives (6-38) between resveratrol and chalcone possessing piperazine moiety have been synthesized, and in vitro anti-inflammatory activity in lipopolysaccharide (LPS)-stimulated RAW-264.7 macrophages and anti-proliferative effect on a panel of human tumor cell lines (Hela, A549 and SGC7901) by MTT assay were evaluated.The results demonstrated that the substituents of the NH group of piperazine ring had an obvious influence on biological activities. Especially, compounds 13, 17, 30, 31 and 36 showed good inhibitory effect on the generation of NO compared to dexamethasone. Furthermore, analogs 20, 21, 22 and 25 were found to be the better anti-proliferative effect on 3 human tumor cell lines, which were found to be a better cytotoxic activity to positive control 5-FU. Many compounds displayed low cytotoxic effect on normal cells L02.Further FACs analysis showed that compounds 20 and 25 significantly induced apoptosis in A549 cell. These derivatives were considered as the potential anti-inflammatory and anti-tumor agents.
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