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标题:新型含 2-吡啶乙醇的金(III)配合物的合成、结构表征、对接模拟及体外抗增殖活性 内容:合成、结构表征、对接模拟和体外抗增殖活性的新型金(III)配合物与 2-吡啶乙醇。

Synthesis, structural characterization, docking simulation and in vitro antiproliferative activity of the new gold(III) complex with 2-pyridineethanol.

机构信息

Faculty of Chemistry, Wroclaw University of Science and Technology, Wybrzeże Wyspiańskiego 27, 50-370 Wroclaw, Poland.

Faculty of Chemistry, Wroclaw University of Science and Technology, Wybrzeże Wyspiańskiego 27, 50-370 Wroclaw, Poland.

出版信息

J Inorg Biochem. 2021 Feb;215:111311. doi: 10.1016/j.jinorgbio.2020.111311. Epub 2020 Nov 18.

DOI:10.1016/j.jinorgbio.2020.111311
PMID:33246642
Abstract

Gold(III) complex containing 2-pyridineethanol has been synthesized and characterized structurally by single crystal X-ray diffraction, vibrational spectroscopy, H NMR spectroscopy, electrochemical study, and DFT calculations. The Au(III) ion is four coordinated with one N-donor ligand (L) and three Cl anions. The Okuniewski's (τ'0.018) has been used to estimate the angular distortion from ideal square planar geometry. The vibrational spectroscopy studies, in the solid state and DMSO solution and cyclic voltammetry, have been performed to determine its stability and redox activity, respectively. A complete assignment of the IR and Raman spectra has been made based on the calculated potential energy distribution (PED). The theoretical calculations have been made for two functionals and several basis sets. The compound has been evaluated for its antiproliferative properties in a human lung adenocarcinoma cell line (A549), mouse colon carcinoma (CT26), human breast adenocarcinoma (MCF-7), human prostate carcinoma derived from the metastatic site in the brain (DU-145), and PANC-1 human pancreas/duct carcinoma cell line and non-tumorigenic cell lines: HaCat (human keratinocyte), and HEK293T (human embryonic kidney). Au(III) complex cytotoxicity is significantly against A549 and MCF-7 cells as in the reference drug: cisplatin. Studies of the interactions of Au(III) complex with DNA, HSA (human serum albumin) have been performed. The results from modeling docking simulations indicate that the title complex exerts anticancer effects in vitro based on different mechanisms of action to compare with cisplatin.

摘要

合成了一种含有 2-吡啶乙醇的金(III)配合物,并通过单晶 X 射线衍射、振动光谱、核磁共振波谱、电化学研究和 DFT 计算对其结构进行了表征。Au(III) 离子与一个 N-供体配体 (L) 和三个 Cl 阴离子四配位。Okuniewski(τ'0.018)被用来估计从理想的正方形平面几何结构的角度扭曲。振动光谱研究分别在固态和 DMSO 溶液以及循环伏安法中进行,以确定其稳定性和氧化还原活性。根据计算的势能分布 (PED),对 IR 和 Raman 光谱进行了完整的归属。理论计算是针对两种功能和几种基组进行的。该化合物已在人肺腺癌细胞系(A549)、小鼠结肠癌细胞(CT26)、人乳腺癌细胞系(MCF-7)、源自大脑转移部位的人前列腺癌细胞系(DU-145)和 PANC-1 人胰腺/胆管癌细胞系和非致瘤细胞系中进行了抗增殖性能的评估:HaCat(人角质形成细胞)和 HEK293T(人胚肾)。与参考药物顺铂相比,金(III)配合物对 A549 和 MCF-7 细胞的细胞毒性明显。已经研究了金(III)配合物与 DNA、HSA(人血清白蛋白)的相互作用。建模对接模拟的结果表明,与顺铂相比,标题配合物基于不同的作用机制发挥体外抗癌作用。

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