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硫代氨基脲和萘普生的银(I)金属药物:生物相容性、抗增殖活性以及与表皮生长因子受体、血管内皮生长因子受体2和赖氨酰氧化酶受体的相互作用研究

Silver(I) metallodrugs of thiosemicarbazones and naproxen: biocompatibility, anti-proliferative activity and interaction studies with EGFR, VEGFR2 and LOX receptors.

作者信息

Bharathi Sundaram, Mahendiran Dharmasivam, Kumar Raju Senthil, Choi Hyo Jeong, Gajendiran Mani, Kim Kyobum, Rahiman Aziz Kalilur

机构信息

Department of Chemistry, The New College (Autonomous), University of Madras, Chennai 600 014, India.

Molecular Pharmacology and Pathology Program, Department of Pathology, Bosch Institute, University of Sydney, Sydney 2006, Australia.

出版信息

Toxicol Res (Camb). 2020 Mar 11;9(1):28-44. doi: 10.1093/toxres/tfaa001. eCollection 2020 Feb.

Abstract

Four new heteroleptic silver(I) complexes with the general formula [Ag(L)(nap)] (-), where L =  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. 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 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 π-pair interactions with the active site of epidermal growth factor receptor, vascular endothelial growth factor receptor 2 and lipoxygenase receptors.

摘要

合成并表征了四种通式为[Ag(L)(nap)] (-)的新型异配体银(I)配合物,其中L = 2-(1-(4-取代苯基)亚乙基)肼基甲硫酰胺,nap = 萘普生。由密度泛函理论和紫外-可见光谱研究确定的几何参数表明银(I)离子周围为扭曲的四面体几何构型。傅里叶变换红外(FT IR)光谱证明萘普生羧基氧原子与银(I)离子呈不对称双齿配位模式。这些配合物在72小时内稳定,并对正常人皮肤成纤维细胞的生物相容性进行了分析,结果表明在高达100 ng/ml的浓度下具有无毒性质。通过MTT法测试了这些配合物对三种人类癌细胞系和一种非致瘤性人类乳腺上皮细胞系(MCF-10a)的抗增殖活性,其中该配合物表现出增强的活性。通过吖啶橙/溴化乙锭和Hoechst 33258染色法观察到的形态变化揭示了这些配合物的诱导凋亡能力。分子对接研究表明,它们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存在氢键、疏水和π-对相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c561/7233324/b2b08f954b4f/tfaa001ga.jpg

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