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Studies of the Antiproliferative Activity of Ruthenium (II) Cyclopentadienyl-Derived Complexes with Nitrogen Coordinated Ligands

机译:氮配体配体钌(II)环戊二烯基衍生的配合物的抗增殖活性研究

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摘要

Four cationic ruthenium(II) complexes with the formula [Ru(η 5-C5H5)(PPh3)2]+, with L = 5-phenyl-1H-tetrazole (TzH) >1, imidazole (ImH) >2, benzo[1,2-b;4,3-b′] dithio-phen-2-carbonitrile (Bzt) >3, and [5-(2-thiophen-2-yl)-vinyl]-thiophene-2-carbonitrile] (Tvt) >4 were prepared and characterized in view to evaluate their potentialities as antitumor agents. Studies by Circular Dichroism indicated changes in the secondary structure of ct-DNA. Changes in the tertiary structure of pBR322 plasmid DNA were also observed in gel electrophoresis experiment and the images obtained by atomic force microscopy (AFM) suggest strong interaction with pBR322 plasmid DNA; the observed decreasing of the viscosity with time indicates that the complexes do not intercalate between DNA base pairs. Compounds >1, >2, and >3 showed much higher cytotoxicity than the cisplatin against human leukaemia cancer cells (HL-60 cells).
机译:四种阳离子钌(II)配合物,其式为[Ru(η 5 -C5H5)(PPh3)2] sup> + ,L = 5-苯基-1H-四唑( TzH)> 1 ,咪唑(ImH)> 2 ,苯并[1,2-b; 4,3-b']二硫代苯-2-甲腈(Bzt)<制备了strong> 3 和[5-(2-噻吩-2-基-乙烯基)-噻吩-2-甲腈](Tvt)> 4 并进行了表征,以进行评估它们作为抗肿瘤药的潜力。圆二色性的研究表明,ct-DNA的二级结构发生了变化。在凝胶电泳实验中还观察到了pBR322质粒DNA的三级结构的变化,原子力显微镜(AFM)获得的图像表明与pBR322质粒DNA有很强的相互作用。观察到的粘度随时间的降低表明复合物没有插入DNA碱基对之间。化合物> 1 ,> 2 和> 3 显示出比顺铂对人类白血病癌细胞(HL-60细胞)更高的细胞毒性。

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