香豆素
化学
细胞凋亡
活性氧
体外
IC50型
细胞培养
细胞毒性T细胞
铅化合物
污渍
药品
细胞毒性
细胞生长
立体化学
药理学
组合化学
生物化学
生物
基因
有机化学
遗传学
作者
Jing Zhang,Ya-Ling Tan,Guorong Li,Lexian Chen,Minyi Nie,Zhaohua Wang,Hong Ji
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2021-02-03
卷期号:26 (4): 786-786
被引量:35
标识
DOI:10.3390/molecules26040786
摘要
Coumarins possesses immeasurable antitumor potential with minimum side effects depending on the substitutions on the basic nucleus, which exhibits great prospects for antitumor drug development. In an attempt to develop novel antitumor candidates, a series of coumarin sulfonamides and amides derivatives were designed and synthetized. The majority of these derivatives showed good cytotoxic activity against MDA-MB-231 and KB cell lines, among which compound 9c was the most potent against MDA-MB-231 cells, with IC50 value of 9.33 μM, comparable to 5-fluorouracil. Further investigation revealed that compound 9c had versatile properties against tumors, including inhibition of cell migration and invasion as well as inducing apoptosis. Reactive oxygen species (ROS) assay and western blotting analysis suggested that compound 9c promoted cancer cell apoptosis by increasing ROS levels and upregulating the expression of caspase-3 in MDA-MB-231 cells. These results indicated that compound 9c could be promising lead compound for further antitumor drug research.
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