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首页> 外文期刊>Inorganica Chimica Acta >Synthesis of redox-active ferrocene pyrazole conjugates and their cytotoxicity in human mammary adenocarcinoma MCF-7 cells
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Synthesis of redox-active ferrocene pyrazole conjugates and their cytotoxicity in human mammary adenocarcinoma MCF-7 cells

机译:氧化还原活性二茂铁吡唑共轭物的合成及其对人乳腺癌MCF-7细胞的细胞毒性

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The redox-active ferrocenoyl modified pyrazole ligand (3-Fc-AMP) readily coordinates to a variety of transition metal ions. Here, we describe our findings regarding the synthesis and structural characterization of iron and cobalt complexes of Fc-AMP, and the cytotoxicity profiles of these chemicals in vitro. Using the human mammary adenocarcinoma MCF-7 cell line we show that the free ligand and three metal complexes induced cytotoxicity with calculated LC(50)s ranging from 45.8 to 73.2 mu M. The toxicity of the complexes decreased as the redox potential increased. The present study demonstrates the potential chemotherapeutic promise of metal complexes of a redox-active ferrocenoyl modified pyrazole ligand on human cancer cells. (c) 2005 Elsevier B.V. All rights reserved.
机译:氧化还原活性的二茂铁酰基修饰的吡唑配体(3-Fc-AMP)易于与各种过渡金属离子配位。在这里,我们描述有关Fc-AMP的铁和钴复合物的合成和结构表征以及这些化学试剂在体外的细胞毒性谱的发现。使用人类乳腺腺癌细胞MCF-7,我们显示了游离配体和三种金属配合物诱导的细胞毒性,计算的LC(50)范围为45.8至73.2μM。随着氧化还原电位的增加,配合物的毒性降低。本研究证明了在人类癌细胞上具有氧化还原活性的二茂铁酰基修饰的吡唑配体的金属配合物的潜在化学治疗前景。 (c)2005 Elsevier B.V.保留所有权利。

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