蛇床子素
体外
细胞培养
化学
细胞毒性
生物测定
G2水电站
IC50型
癌细胞系
肝细胞癌
细胞
MTT法
肝癌
生物化学
分子生物学
癌症
癌细胞
生物
癌症研究
齐墩果酸
医学
病理
替代医学
遗传学
作者
Xiao Liu,Lu Sun,Qinghua Liu,Baoquan Chen,Yu‐Ming Liu
出处
期刊:Mini-reviews in Medicinal Chemistry
[Bentham Science]
日期:2020-03-05
卷期号:20 (3): 252-257
被引量:3
标识
DOI:10.2174/1389557519666191010091612
摘要
Based on the biological significance of hederagenin-type saponins found in our previous investigation, a series of new hederagenin derivatives were designed and synthesized.Their in vitro antiproliferative activities were evaluated against the HepG2 liver cancer cell line and normal cell line L929 by MTT assay.The preliminary bioassay results demonstrated that all the tested compounds 1-7 showed potent anti-hepatoma activities, and some compounds exhibited better effects than 5-fluorouracil against human hepatocellular carcinoma HepG2 cell line. Furthermore, compound 5 showed a significant antihepatoma activity against HepG2 cells with an IC50 value of 1.88 µM. Besides, all of the tested compounds showed a low cytotoxic effect against the normal cell line L929.All the compounds 1-7 displayed superior selectivity against human hepatocellular carcinoma HepG2 cell line, and the results suggest that the structural modifications of C ring on the hederagenin backbone are vital for modulating anti-hepatoma activities.
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