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Cu(II) Benzoylpyridine Thiosemicarbazone Complexes: Inhibition of Human Topoisomerase IIα and Activity against Breast Cancer Cells 被引量:1
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作者 Jennifer D. Conner Wathsala Medawala +6 位作者 madison t. stephens William H. Morris Joseph E. Deweese Patrick L. Kent Jeffery J. Rice Xiaohua Jiang Edward C. Lisic 《Open Journal of Inorganic Chemistry》 2016年第2期146-154,共9页
The focus of this research is on the study of a series of copper (II) benzoylpyridine thiosemicarbazone complexes. Of the six benzoylpyridine thiosemicarbazone ligands used in this study, two are reported for the firs... The focus of this research is on the study of a series of copper (II) benzoylpyridine thiosemicarbazone complexes. Of the six benzoylpyridine thiosemicarbazone ligands used in this study, two are reported for the first time;2-benzoylpyridine tert-butyl thiosemicarbazone (BZP-tBTSC), and 2-benzoylpyridine benzyl thiosemicarbazone (BZP-BzTSC). Once characterized by NMR, melting point, and MS, these mono-anionic tridentate ligands were then reacted with Cu<sup>2+</sup> to form the new square planar metal complexes [Cu(BZP-tBTSC)Cl] and [Cu(BZP-BzTSC)Cl]. All of the copper complexes display marked inhibition of human topoisomerase IIα. The [Cu(BZP-tBTSC)Cl] complex shows marked activity against human breast cancer cell lines. 展开更多
关键词 Topoisomerase IIα Alpha-(N)-Heterocyclic Thiosemicarbazones Breast Cancer Cells
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