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新型查尔酮酰胺苯并噻唑类化合物的合成及生物活性评价。

Synthesis and biological evaluation of combretastatin-amidobenzothiazole conjugates as potential anticancer agents.

机构信息

Division of Organic Chemistry, CSIR-Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500 607, India.

出版信息

Eur J Med Chem. 2012 Oct;56:166-78. doi: 10.1016/j.ejmech.2012.08.021. Epub 2012 Aug 23.

Abstract

A series of combretastatin-amidobenzothiazole conjugates have been synthesized and evaluated for their anticancer activity. All these compounds exhibited significant anticancer activity and the most potent compound (11a) showed GI(50) values ranging 0.019-11 μM. Biological studies such as cell cycle distribution, effect on tubulin polymerization and effect on ERK signalling pathway have been examined in MCF-7 cell line. FACS analysis revealed that these compounds induced cell cycle arrest at G2/M phase. Compound 11a showed significant effect on tubulin polymerization and affected the ERK signalling pathway that result in the decreased levels of ERK1/2, p-ERK and c-Jun proteins. Docking experiments have shown that the active molecules interact and bind well in the ATP binding pocket of ERK protein.

摘要

一系列的 combretastatin-酰胺苯并噻唑缀合物已经被合成并评估了它们的抗癌活性。所有这些化合物都表现出显著的抗癌活性,其中最有效的化合物(11a)表现出 GI(50) 值在 0.019-11 μM 之间。在 MCF-7 细胞系中进行了细胞周期分布、对微管蛋白聚合的影响和对 ERK 信号通路的影响等生物学研究。FACS 分析显示,这些化合物诱导细胞周期停滞在 G2/M 期。化合物 11a 对微管蛋白聚合有显著影响,并影响 ERK 信号通路,导致 ERK1/2、p-ERK 和 c-Jun 蛋白水平降低。对接实验表明,活性分子在 ERK 蛋白的 ATP 结合口袋中相互作用并结合良好。

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