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首页> 外文期刊>Journal of biological inorganic chemistry: JBIC: a publication of the Society of Biological Inorganic Chemistry >Cytotoxic activity of expanded coordination bis-thiosemicarbazones and copper complexes thereof
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Cytotoxic activity of expanded coordination bis-thiosemicarbazones and copper complexes thereof

机译:扩展配位的双硫代半氨基甲酮及其铜配合物的细胞毒活性

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A series of bis-thiosemicarbazone agents with coordinating groups capable of multiple metal coordination modes has been generated and evaluated for potential cytotoxic effects against melanoma (MelRm) and breast adenocarcinoma (MCF-7) cell lines. The bis-thiosemicarbazones in this study generally demonstrated superior cytotoxic activity against MelRm than MCF-7 in the absence of metal ion supplementation, but in most cases could not be considered superior to the reference thiosemicarbazone Dp44mT. The key structural features for the cytotoxic activity were the central metal binding atom on the aromatic core, the thiocarbonyl residue and the nature of substitution on the N4-terminus in terms of size and lipophilicity. The cytotoxicity of bis-thiosemicarbazone ligands improved significantly with Cu(II) supplementation, particularly against MCF-7 cells. The mechanism of cytotoxicity of bis-thiosemicarbazones was proposed to be dependent on the combined effect of metal mobilisation and ROS generation which is so called a "double-punch effect".
机译:已经产生了一系列具有能够以多种金属配位模式进行配位的配位基团的双硫代半脲类药物,并评估了其对黑素瘤(MelRm)和乳腺癌(MCF-7)细胞系的潜在细胞毒性作用。在没有添加金属离子的情况下,该研究中的双硫半碳杂唑酮一般表现出比MCF-7更好的针对MelRm的细胞毒活性,但在大多数情况下,不能认为它比参考硫半碳a Dp44mT优越。细胞毒性活性的关键结构特征是芳香核上的中心金属结合原子,硫代羰基残基以及在N4末端的大小和亲脂性方面的取代性质。补充Cu(II),尤其是针对MCF-7细胞,可大大改善双硫半脲配体的细胞毒性。有人提出,双硫代半氨基甲酮的细胞毒性机制取决于金属动员和活性氧生成的联合作用,即所谓的“双穿孔效应”。

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