Suppr超能文献

含 2-甲酰基吡啶缩硫代氨基脲和 1,10-菲啰啉的三元银(i)配合物的细胞毒性和细胞凋亡作用。

Cytotoxic and apoptotic effects of ternary silver(i) complexes bearing 2-formylpyridine thiosemicarbazones and 1,10-phenanthroline.

机构信息

Department of General and Inorganic Chemistry, Department of Analytical Chemistry, UNESP - São Paulo State University, Institute of Chemistry, CEP 14800-060 Araraquara, SP, Brazil.

Department de Gerontology, Federal University of São Carlos, CEP 13565-905 São Carlos, SP, Brazil.

出版信息

Dalton Trans. 2020 Apr 28;49(16):5264-5275. doi: 10.1039/d0dt00253d.

Abstract

New silver(i) compounds containing 2-formylpyridine-N(4)-R-thiosemicarbazones and 1,10-phenanthroline (phen) were synthesized and characterized by spectroscopic techniques (IR and NMR), elemental analysis, ESI-MS and molar conductance measurements. In these complexes, both phen and thiosemicarbazone ligands are coordinated in a chelating bidentate fashion. Compounds 1-3 not only showed good in vitro antiproliferative activity against human lung (A549) and breast tumor cells (MDA-MB-231 and MCF-7), with IC50 values ranging from 1.49 to 20.90 μM, but were also demonstrated to be less toxic towards human breast non-tumor cells (MCF-10A). Cellular uptake studies indicated that compounds 1-3 were taken up by the MDA-MB-231 cells in 6 hours. Cell death assays in the MDA-MB-231 cells were conducted with compound 1 aiming to evaluate its effects on cell morphology, induction of apoptosis, the cell cycle, reactive oxygen species (ROS) formation and mitochondrial membrane potential (Δψm). Compound 1 caused morphological changes, such as cell shrinkage and rounding, increased the sub-G1 phase population, and induced apoptotic cell death, ROS formation and loss of mitochondrial membrane potential (Δψm). DNA binding results revealed that 1 interacted with the ct-DNA minor groove. Complexes 1-3 also exhibited good in vitro activity against M. tuberculosis H37Rv, with MIC values ranging from 3.37 to 4.65 μM.

摘要

新的含 2-甲酰基吡啶-N(4)-R-缩氨基硫脲和 1,10-菲咯啉(phen)的银(I)配合物被合成并通过光谱技术(IR 和 NMR)、元素分析、ESI-MS 和摩尔电导率测量进行了表征。在这些配合物中,phen 和缩氨基硫脲配体都以螯合双齿方式配位。化合物 1-3 不仅对人肺癌(A549)和乳腺癌肿瘤细胞(MDA-MB-231 和 MCF-7)具有良好的体外抗增殖活性,IC50 值范围为 1.49 至 20.90 μM,而且对人乳腺癌非肿瘤细胞(MCF-10A)的毒性也较低。细胞摄取研究表明,化合物 1-3 在 6 小时内被 MDA-MB-231 细胞摄取。为了评估化合物 1 对 MDA-MB-231 细胞形态、诱导细胞凋亡、细胞周期、活性氧(ROS)形成和线粒体膜电位(Δψm)的影响,在 MDA-MB-231 细胞中进行了细胞死亡实验。化合物 1 导致细胞形态发生变化,如细胞收缩和变圆,增加了亚 G1 期细胞群,并诱导了细胞凋亡、ROS 形成和线粒体膜电位(Δψm)的丧失。DNA 结合结果表明,1 与 ct-DNA 小沟相互作用。配合物 1-3 对结核分枝杆菌 H37Rv 也具有良好的体外活性,MIC 值范围为 3.37 至 4.65 μM。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验