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首页> 外文期刊>Toxicology Research >Silver(I) metallodrugs of thiosemicarbazones and naproxen: biocompatibility, in vitro anti-proliferative activity and in silico interaction studies with EGFR, VEGFR2 and LOX receptors
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Silver(I) metallodrugs of thiosemicarbazones and naproxen: biocompatibility, in vitro anti-proliferative activity and in silico interaction studies with EGFR, VEGFR2 and LOX receptors

机译:硫代蓟虫和萘普生的银(I)Metallodrugs:生物相容性,体外抗增殖活动和硅互动研究与EGFR,VEGFR2和LOX受体

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摘要

Four new heteroleptic silver(I) complexes with the general formula [Ag(L1-4)(nap)] (1-4), where L1-4 = 2-(1-(4-substitutedphenyl)ethylidene)hydrazinecarbothioamide and nap = naproxen, have been synthesized and characterized. The geometric parameters determined from density functional theory and UV-Vis studies indicate distorted tetrahedral geometry around silver(I) ion. Fourier transform infrared (FT IR) spectra evidenced asymmetric bidentate coordination mode of carboxyl oxygen atoms of naproxen with silver(I) ion. The complexes are stable for 72 h and biocompatibility was analysed towards normal human dermal fibroblast cells, which showed non-toxic nature up to 100 ng/ml. In vitro anti-proliferative activity of the complexes by MTT assay was tested against three human cancerous cell lines and one non-tumorigenic human breast epithelial cell line (MCF-10a) in which the complex 4 exhibited enhanced activity. The morphological changes observed by acridine orange/ethidium bromide and Hoechst 33258 staining method reveal apoptosis-inducing ability of the complexes. The molecular docking studies suggest hydrogen bonding, hydrophobic and p-pair interactions with the active site of epidermal growth factor receptor, vascular endothelial growth factor receptor 2 and lipoxygenase receptors.
机译:具有通式[Ag(L1-4)(NAP)](1-4)的四种新的异孔银(I)配合物,其中L1-4 = 2-(1-(4-取代烯基)乙基)肼肼和NAP =萘普生已被合成和特征。从密度泛函理论和UV-VIS研究确定的几何参数表示银(I)离子周围的四面体几何形状。傅里叶变换红外(FT IR)光谱证明了用银(I)离子的萘锡羧基原子的不对称双齿配位模式。复合物稳定72小时,分析生物相容性朝向正常人的皮肤成纤维细胞,其显示出无毒性高达100ng / mL。通过MTT测定对复合物的体外抗增殖活性对三种人类癌细胞系和一种非致瘤人乳房上皮细胞系(MCF-10A)进行测试,其中复合体4表现出增强的活性。吖啶橙/乙锭和Hoechst 33258染色方法观察到的形态变化揭示了复合物的凋亡诱导能力。分子对接研究表明与表皮生长因子受体,血管内皮生长因子受体2和脂氧合酶受体的活性位点的氢键,疏水和对相互作用。

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