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首页> 外文期刊>Bioorganic and Medicinal Chemistry >Novel acyclic enediynes inhibit Cyclin A and Cdc25C expression and induce apoptosis phenomenon to show potent antitumor proliferation
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Novel acyclic enediynes inhibit Cyclin A and Cdc25C expression and induce apoptosis phenomenon to show potent antitumor proliferation

机译:新型无环烯二炔抑制Cyclin A和Cdc25C表达并诱导细胞凋亡现象,显示有效的抗肿瘤增殖

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摘要

A series of acyclic enediynes showing significant inhibition on the growth of tumor cancer is disclosed. To investigate the structure-activity relationship, compounds 12-33 were synthesized. Among them, compound 17 showed most potent growth inhibition activity against all tumor cell lines at low concentration, such as SR (0.4 μM) and MDA-MB-435 (0.8 μM), and almost completely blocked cell cycle in G2/M phase via controlling Cyclin A and Cdc25C expression. On the other hand, compound 29 showed potent induced apoptosis activity by inducing activation of caspase-3, -8, and -9. Thus, this article disclosed a new multiple-protein regulator in cell cycle regulation and induced apoptosis to achieve the goal of anticancer drug.
机译:公开了一系列对肿瘤癌的生长具有显着抑制作用的无环烯二炔。为了研究结构-活性关系,合成了化合物12-33。其中,化合物17对所有低浓度的肿瘤细胞系,如SR(0.4μM)和MDA-MB-435(0.8μM)表现出最强的生长抑制活性,并且几乎完全阻断了G2 / M期的细胞周期控制细胞周期蛋白A和Cdc25C的表达。另一方面,化合物29通过诱导caspase-3,-8和-9的活化而显示出有效的诱导的细胞凋亡活性。因此,本文公开了一种新型的多蛋白调节剂,可以调控细胞周期并诱导细胞凋亡,从而达到抗癌药物的目的。

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