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锌-甲硝唑的两种DNA结合模式及其作为强效抗癌剂的生物学评价

Two DNA binding modes of a zinc-metronidazole and biological evaluation as a potent anti-cancer agent.

作者信息

Ahmadi Farhad, Shabrandi Nosaibeh, Hosseinzadeh Leilah, Azizian Homa

机构信息

a Department of Medicinal Chemistry Faculty of Pharmacy , Kermanshah University of Medical Sciences , Kermanshah , Iran.

b Physiology Research Center Iran University of Medical Sciences , Tehran , Iran.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2019;38(7):449-480. doi: 10.1080/15257770.2018.1562073. Epub 2019 Jan 28.

Abstract

A complex of metronidazole (MTZ) with zinc ion was synthesized and characterized by UV-Vis, Fourier transform infrared (FT-IR), H-NMR, X-ray crystallography and thermal gravimetric-differential thermal analysis (TG-DTA). The cytotoxicity effect of the synthesized complex investigated over SKNMC, A549, MCF-7, and MCDK cell lines and the results have shown that it has high cytotoxic potential over cancer cell lines. In order to clarify the mechanism of cell cytotoxicity, the oxidative stress and binding of the complex to the calf thymus-DNA studied by evaluating the intrinsic binding constant and defining thermodynamic parameters of complex over the DNA accompanying with in silico molecular modeling method. For this purpose, the complex optimized at the B3LYP/LANL2DZ level and docked over the DNA structure. The results revealed that the metronidazole-zinc complex interacted with DNA via hydrogen binding and electrostatic interaction to the minor groove region and phosphate backbone of DNA, respectively.

摘要

合成了甲硝唑(MTZ)与锌离子的配合物,并通过紫外可见光谱、傅里叶变换红外光谱(FT-IR)、氢核磁共振光谱(H-NMR)、X射线晶体学以及热重-差热分析(TG-DTA)对其进行了表征。研究了合成配合物对SKNMC、A549、MCF-7和MCDK细胞系的细胞毒性作用,结果表明它对癌细胞系具有高细胞毒性潜力。为了阐明细胞毒性机制,通过评估内在结合常数并确定配合物与小牛胸腺DNA结合的热力学参数,同时结合计算机模拟分子建模方法,研究了该配合物的氧化应激以及与小牛胸腺DNA的结合情况。为此,在B3LYP/LANL2DZ水平上对配合物进行了优化,并将其对接至DNA结构上。结果表明,甲硝唑-锌配合物分别通过氢键和静电相互作用与DNA的小沟区域和磷酸骨架相互作用。

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