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基于吲哚的半夹心型催化活性配合物的合成、表征及体外抗癌活性研究。

Synthesis, Characterisation and In Vitro Anticancer Activity of Catalytically Active Indole-Based Half-Sandwich Complexes.

机构信息

School of Chemistry and Biosciences, University of Bradford, Bradford BD1 7DP, UK.

Department of Chemistry, University of Ilorin, Ilorin P.M.B 1515, Nigeria.

出版信息

Molecules. 2020 Oct 3;25(19):4540. doi: 10.3390/molecules25194540.

Abstract

The synthesis, characterisation and evaluation of the in vitro cytotoxicity of four indole-based half-sandwich metal complexes towards two ovarian cancer cell lines (A2780 and A2780cisR) and one normal prostate cell line (PNT2) are presented herein. Although capable of inducing catalytic oxidation of NADH and able to reduce NAD with high turnover frequencies, in cells and in the presence of sodium formate, these complexes also strongly interact with biomolecules such as glutathione. This work highlights that efficient out-of-cells catalytic activity might lead to higher reactivity towards biomolecules, thus inhibiting the in-cells catalytic processes.

摘要

本文介绍了四种基于吲哚的半夹心金属配合物的合成、表征及其对两种卵巢癌细胞系(A2780 和 A2780cisR)和一种正常前列腺细胞系(PNT2)的体外细胞毒性的评价。尽管这些配合物能够诱导 NADH 的催化氧化,并具有高转化频率还原 NAD,但在细胞中和存在甲酸钠的情况下,它们也会与谷胱甘肽等生物分子强烈相互作用。这项工作强调了高效的细胞外催化活性可能导致对生物分子更高的反应性,从而抑制细胞内的催化过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceba/7583056/95d1ee88ca8c/molecules-25-04540-g001.jpg

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