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合成、表征、理论、分子对接及新型苯胺取代芳酰基硒脲的 Ru(II)(--柠檬烯)配合物的生物活性研究。

Synthesis, characterization, theoretical, molecular docking and biological activity studies of Ru(II) (--cymene) complexes with novel aniline substituted aroyl selenoureas.

机构信息

Department of Chemistry, National Institute of Technology, Tiruchirappalli, Tamil Nadu, India.

Chemistry Division, H&S Department, Malla Reddy Engineering College for Women (Autonomous Institution), Hyderabad, Telangana, India.

出版信息

J Biomol Struct Dyn. 2021 Aug;39(12):4346-4361. doi: 10.1080/07391102.2020.1778531. Epub 2020 Jun 29.

Abstract

A sequence of aroyl selenourea ligands ( substituted by aniline and their Ru(II) (--cymene) complexes , [Ru(II) (--cymene) L] (L = monodentate aroyl selenourea ligand) have been synthesized and characterized the composition of the ligands and their metal complexes. The molecular structures of ligand and complex were also confirmed by single XRD crystal method. The single-crystal XRD study showed that aroyl selenourea ligand coordinates with Ru Se novel neutral monodentate atom. DNA interaction studies were investigated by Fluorescence and UV-Visible spectroscopic methods which showed that the intercalative mode of binding is in the order of with Ru(II) (--cymene) complexes. Spectroscopic methods have been used for measuring the binding affinity of bovine serum albumin to complex. Moreover, the cytotoxic study of complexes ( were evaluated against HeLa S3, A549, and IMR90 cells, resulting in complexes and showed promising cytotoxic activity against HeLa S3 cell with IC values of 24 and 26 µM, respectively. Also, the morphological changes of HeLa S3 and A549 cells were confirmed by fluorescence microscope in the presence of complexes and using AO (acridine orange, 200 µM) and EB (ethidium bromide, 100 µM). In addition, the docking results strongly support the protein binding studies of the complexes.Communicated by Ramaswamy H. Sarma.

摘要

已合成了一系列芳酰基硒脲配体(由苯胺取代及其 Ru(II)(--柠檬烯)配合物,[Ru(II)(--柠檬烯)L](L=单齿芳酰基硒脲配体),并对配体和其金属配合物的组成进行了表征。通过单晶 XRD 方法还确定了配体和配合物的分子结构。单晶 XRD 研究表明,芳酰基硒脲配体与 Ru Se 新型中性单齿原子配位。通过荧光和紫外可见光谱法研究了 DNA 相互作用,结果表明结合方式为插入模式,且 Ru(II)(--柠檬烯)配合物的结合顺序为。光谱法用于测量牛血清白蛋白与配合物的结合亲和力。此外,还评估了配合物(对 HeLa S3、A549 和 IMR90 细胞的细胞毒性,结果表明配合物 和 对 HeLa S3 细胞具有良好的细胞毒性活性,IC 值分别为 24 和 26 μM。此外,在存在配合物 和 的情况下,通过荧光显微镜观察到 HeLa S3 和 A549 细胞的形态变化,使用 AO(吖啶橙,200 μM)和 EB(溴化乙锭,100 μM)。此外,对接结果强烈支持配合物的蛋白质结合研究。由 Ramaswamy H. Sarma 传达。

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