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

一种新型铜(II)配合物被鉴定为对抗结直肠癌和乳腺癌细胞的强效药物,同时也是人拓扑异构酶IIα的毒性抑制剂。

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Abstract

A novel complex, [Cu(acetylethTSC)Cl]Cl•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 IIα, which may account for the observed anti-cancer effects.

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