首页> 外文期刊>Journal of inorganic and organometallic polymers and materials >Synthesis, Characterization for New Nanometric VO(Ⅱ)-Thioacetanilide Complexes by, Spectral, Thermal, Molecular Computations and DNA Interaction Study Beside Promising Antitumor Activity
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Synthesis, Characterization for New Nanometric VO(Ⅱ)-Thioacetanilide Complexes by, Spectral, Thermal, Molecular Computations and DNA Interaction Study Beside Promising Antitumor Activity

机译:通过有望的抗肿瘤活性,通过光谱,热,分子计算和DNA相互作用研究,合成,表征新型纳米VO(Ⅱ)-硫代乙酰苯胺配合物

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摘要

A novel series, of thioacetanilide derivatives (4a-e), was synthesized and fully characterized. Their corresponding VO(II) complexes, were prepared and inspected by all analytical, spectral and computational techniques. From IR spectral analysis, poly dentate mode of bonding, was proposed for all organic ligands towards two central atoms. The octahedral arrangement configuration, was suggested for all complexes, based on; UV-Vis, ESR and magnetic measurements. TGA and DTA analysis, built a good assertion on the presence of solvent molecules, attached with the complex particles. The molecular modeling technique, excreted the best structural forms for all tested compounds. Moreover, essential computational parameters were estimated, to verify the molecular formulae. Molecular docking study, was concerning with the inhibition feature against 3s7s and 3gcw proteins, belonging to breast and liver cancer cells, respectively. The computed parameters introduced a promising activity for some tested derivatives. Furthermore, the experimental antitumor screening for VO(II) complexes, versus HepG-2 and MCF-7 cell lines, displayed superiority for [(VO)(2)(SO4)(2)(AETA)(H2O)(2)]3H(2)O complex in comparing to cisplatin (standard drug). As well as, the genotoxicity results, coincide excellently with antitumor result.
机译:合成并充分表征了一系列新的硫代乙酰苯胺衍生物(4a-e)。通过所有分析,光谱和计算技术制备并检查了它们相应的VO(II)配合物。通过红外光谱分析,提出了所有朝向两个中心原子的有机配体的多齿键合模式。建议基于所有配合物的八面体排列配置; UV-Vis,ESR和磁测量。 TGA和DTA分析对与复杂颗粒连接的溶剂分子的存在建立了很好的断言。分子建模技术为所有测试的化合物排除了最佳的结构形式。此外,估计必要的计算参数,以验证分子式。分子对接研究涉及对分别属于乳腺癌和肝癌细胞的3s7s和3gcw蛋白的抑制作用。计算出的参数为一些经过测试的衍生物引入了有希望的活性。此外,相对于HepG-2和MCF-7细胞系,针对VO(II)复合物的实验性抗肿瘤筛选显示出对[(VO)(2)(SO4)(2)(AETA)(H2O)(2)]的优越性。与顺铂(标准药物)相比,具有3H(2)O配合物。以及,遗传毒性结果与抗肿瘤结果极佳地吻合。

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