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新型配合物顺式-(Cl,Cl)[RuIICl2(NO+)(三联吡啶)]Cl的合成、表征、体外抗肿瘤活性、DNA结合特性及电子结构(密度泛函理论)

Synthesis, characterization, in vitro antitumor activity, DNA-binding properties and electronic structure (DFT) of the new complex cis-(Cl,Cl)[RuIICl2(NO+)(terpy)]Cl.

作者信息

Karidi Konstantina, Garoufis Achilleas, Tsipis Athanassios, Hadjiliadis Nick, den Dulk Hans, Reedijk Jan

机构信息

Laboratory of Inorganic and General Chemistry, Department of Chemistry, University of Ioannina, Greece.

出版信息

Dalton Trans. 2005 Apr 7(7):1176-87. doi: 10.1039/b418838a. Epub 2005 Feb 18.

Abstract

The complex cis-(Cl,Cl)-[RuCl2(terpy)(NO)]Cl (1) has been synthesized by the reaction of [RuCl3(H2O)2(NO)] with terpyridine (terpy) and characterized by various spectroscopic, analytical techniques and using electronic structure calculation (DFT) methods. The cytotoxic activity and the DNA-binding properties of have also been studied using biochemical techniques. The results establish unequivocally that corresponds to a so-called [RuNO]6 species, which readily releases the nitrosyl ligand upon irradiation with a mercury lamp in acetonitrile solution. DFT calculations provided a satisfactory description of structural, bonding, electronic and related properties of the new compound and throw light on the mechanism of the photo-induced NO release. Screening on A2780 (human ovarian carcinoma) cell lines showed significant cytotoxicity with an IC50 value of 0.49 microM. 31P and 23Na NMR spectroscopy along with electrophoretic mobility studies illustrated that complex primarily binds by coordination to DNA without any pi-interaction between the planar terpy ligand and the DNA bases, while weak electrostatic interactions could not be excluded. Studies on the inhibition of the restriction enzymes DraI and SmaI revealed that prefers the guanine and cytosine bases of DNA.

摘要

通过[RuCl3(H2O)2(NO)]与三联吡啶(terpy)反应合成了配合物顺式-(Cl,Cl)-[RuCl2(terpy)(NO)]Cl(1),并通过各种光谱、分析技术以及电子结构计算(DFT)方法对其进行了表征。还使用生化技术研究了其细胞毒性活性和DNA结合特性。结果明确证实其对应于一种所谓的[RuNO]6物种,在乙腈溶液中用汞灯照射时它会容易地释放出亚硝酰配体。DFT计算对新化合物的结构、键合、电子及相关性质给出了令人满意的描述,并揭示了光诱导NO释放的机制。对A2780(人卵巢癌)细胞系的筛选显示出显著的细胞毒性,IC50值为0.49微摩尔。31P和23Na NMR光谱以及电泳迁移率研究表明,该配合物主要通过配位与DNA结合,平面三联吡啶配体与DNA碱基之间不存在任何π相互作用,不过不能排除弱静电相互作用。对限制性内切酶DraI和SmaI抑制作用的研究表明,该配合物更倾向于与DNA的鸟嘌呤和胞嘧啶碱基结合。

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