Synthesis and Anticancer Activity of Indolin-2-one Derivatives Bearing the 4-Thiazolidinone Moiety

被引:36
|
作者
Wang, Shuobing [1 ]
Zhao, Yanfang [1 ]
Zhu, Wufu [1 ]
Liu, Ying [1 ]
Guo, Kaixing [1 ]
Gong, Ping [1 ]
机构
[1] Shenyang Pharmaceut Univ, Key Lab Original New Drugs Design & Discovery, Minist Educ, Shenyang 110016, Liaoning, Peoples R China
关键词
Anticancer activity; Indolin-2-one; 4-Thiazolidinone; ANTIPROLIFERATIVE ACTIVITY; CANCER CELLS; INHIBITORS; DISCOVERY; AGENTS; CYTOTOXICITY; RHODANINE; LEUKEMIA; DESIGN; GROWTH;
D O I
10.1002/ardp.201100082
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A novel series of indolin-2-one derivatives containing the 4-thiazolidinone moiety (5a-5p) was synthesized and the cytotoxicity of these derivatives was evaluated in vitro against three human cancer cell lines (HT-29, H460 and MDA-MB-231) by standard MTT assay. Some prepared compounds exhibited significant cytotoxicity against different human cancer cell lines. Several potent compounds were further evaluated against one normal cell line (WI-38). In particular, the promising compound 5h showed remarkable cytotoxicity and selectivity against the HT-29 and H460 cancer cell lines (IC50 = 0.016 mu mol/L, 0.0037 mu mol/L, respectively).
引用
收藏
页码:73 / 80
页数:8
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