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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >New thiazole-2(3H)-thiones containing 4-(3,4,5-trimethoxyphenyl) moiety as anticancer agents
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New thiazole-2(3H)-thiones containing 4-(3,4,5-trimethoxyphenyl) moiety as anticancer agents

机译:新的噻唑-2(3H) - 含有4-(3,4,5-三甲氧基苯基)部分作为抗癌剂

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A new series of thiazole-2(3H)-thiones containing 4-(3,4,5-trimethoxyphenyl) moiety were synthesized as diaryl-heterocylic analogs of combretastatin A-4 with anticancer activity. The cytotoxicity evaluation of synthesized compounds against cancer cell lines (A549, MCF-7 and SKOV3) revealed that most of them had potent cytotoxic activity toward all tested cell lines (IC(50)s < 10 mu g/mL). Among them, 3-(chlorobenzyl) derivatives Sc and 5d showed the best inhibitory effect on MCF-7 cells (IC(50 )values of 1.14 and 2.41 mu g/ml, respectively). Furthermore, the ability of tubulin polymerization inhibition and apoptosis induction were evaluated for the promising compounds Sc and Sd. Results suggested that these compounds remarkably inhibit tubulin polymerization and induce apoptosis resulting in cell death. In vitro studies revealed that these compounds had no significant cytotoxicity against normal cells at the concentrations required for growth inhibition of cancer cells. In vitro biding assay and in silica docking study also confirmed the binding of prototype compound to the colchicine binding site of tubulin. (C) 2019 Elsevier Masson SAS. All rights reserved.
机译:含有4-(3,4,5-三甲氧基苯基)部分的新系列的噻唑-2(3H) - 含有4-(3,4,5-三甲氧基苯基)部分的二芳基芳基A-4与抗癌活性的二芳基杂种类似物合成。对癌细胞系(A549,MCF-7和SKOV3)的合成化合物的细胞毒性评价显示,它们中的大多数对所有测试细胞系(IC(50)S <10μg/ ml)具有有效的细胞毒性活性。其中,3-(氯苄基)衍生物Sc和5d显示了对MCF-7细胞的最佳抑制作用(分别为1.14和2.41μg/ ml的IC(50)值)。此外,评估了对小管蛋白聚合抑制和凋亡诱导的能力,用于备注的化合物SC和SD。结果表明,这些化合物显着抑制阴管蛋白聚合,诱导细胞凋亡导致细胞死亡。体外研究表明,这些化合物在癌细胞生长抑制所需的浓度下对正常细胞没有显着的细胞毒性。体外弯曲测定和二氧化硅对接研究还证实了原型化合物与微蛋白的Colcoicine结合位点的结合。 (c)2019年Elsevier Masson SAS。版权所有。

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