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A novel copper(II) complex identified as a potent drug against colorectal and breast cancer cells and as a poison inhibitor for human topoisomerase II alpha

机译:一种新型铜(II)配合物,被认为是针对结肠直肠癌和乳腺癌细胞的有效药物,并且是人类拓扑异构酶IIα的毒药抑制剂

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摘要

A novel complex, [Cu(acetylethTSC)Cl]Cl center dot 0.25C(2)H(5)OH 1 (where acetylethTSC = (E)-N-ethyl-2-[1-(thiazol-2-yl)ethylidene]hydrazinecarbothioamide), was shown to have anti-proliferative activity against various colon and aggressive breast cancer cell lines. In vitro studies showed that complex 1 acted as a poison inhibitor of human topoisomerase II alpha, which may account for the observed anti-cancer effects. (C) 2015 Elsevier B.V. All rights reserved.
机译:新型复合物[Cu(acetylethTSC)Cl] Cl中心点0.25C(2)H(5)OH 1(其中ethethethC =(E)-N-乙基-2- [1-(噻唑-2-基)亚乙基[肼二甲硫酰胺],被证明对各种结肠和侵袭性乳腺癌细胞系具有抗增殖活性。体外研究表明,复合物1充当人类拓扑异构酶IIα的毒性抑制剂,这可能是观察到的抗癌作用的原因。 (C)2015 Elsevier B.V.保留所有权利。

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