Synthesis and Anticancer Activity of Indolin-2-one Derivatives Bearing the 4-Thiazolidinone Moiety
作者:Shuobing Wang、Yanfang Zhao、Wufu Zhu、Ying Liu、Kaixing Guo、Ping Gong
DOI:10.1002/ardp.201100082
日期:2012.1
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
合成了一系列含有 4-噻唑烷酮部分 (5a-5p) 的新型 indolin-2-one 衍生物,并在体外评估了这些衍生物对三种人类癌细胞系(HT-29、H460 和 MDA-MB-)的细胞毒性。 231) 通过标准 MTT 测定。一些制备的化合物对不同的人类癌细胞系表现出显着的细胞毒性。针对一种正常细胞系 (WI-38) 进一步评估了几种有效化合物。特别是,有前途的化合物 5h 对 HT-29 和 H460 癌细胞系显示出显着的细胞毒性和选择性(IC50 分别为 0.016 µmol/L 和 0.0037 µmol/L)。