Giovagnini Lorena, Sitran Sergio, Castagliuolo Ignazio, Brun Paola, Corsini Maddalena, Zanello Piero, Zoleo Alfonso, Maniero Annalisa, Biondi Barbara, Fregona Dolores
Department of Chemical Sciences, University of Padova, Via Marzolo 1, 35131, Padova, Italy.
Dalton Trans. 2008 Dec 21(47):6699-708. doi: 10.1039/b806341a. Epub 2008 Oct 14.
In recent years, Ru(iii) complexes have emerged as a new class of effective anticancer agents against tumors that proved to be resistant to all other chemotherapeutic drugs currently in clinical use. To extend our previous studies on metal complexes containing sulfur-donor ligands, we report here on the synthesis and characterization, by means of several spectroscopic and analytical techniques, some [Ru(RSDT)(3)] and [Ru(2)(RSDT)(5)]Cl complexes with dithiocarbamato ligands derived from methyl/ethyl/tert-butyl esters of sarcosine. Their electrochemical behaviour was also studied by cyclic voltammetry. All the complexes were tested for their cytotoxicity on a panel of human tumor cell lines showing highly significant antitumor activity. The chemical and biological properties of the newly synthesized complexes, were compared with those of [Ru(DMDT)(3)] and [Ru(2)(DMDT)(5)]Cl species (DMDT = N,N-dimethyldithiocarbamate) whose chemical (not biological) characterization has been already reported in literature.
近年来,钌(III)配合物已成为一类新型有效的抗癌剂,可对抗那些对目前临床使用的所有其他化疗药物均具有抗性的肿瘤。为了扩展我们之前对含硫供体配体的金属配合物的研究,我们在此报告通过几种光谱和分析技术对一些含有由肌氨酸甲酯/乙酯/叔丁酯衍生的二硫代氨基甲酸盐配体的[Ru(RSDT)(3)]和[Ru(2)(RSDT)(5)]Cl配合物的合成与表征。还通过循环伏安法研究了它们的电化学行为。在一组显示出高度显著抗肿瘤活性的人类肿瘤细胞系上测试了所有配合物的细胞毒性。将新合成配合物的化学和生物学性质与[Ru(DMDT)(3)]和[Ru(2)(DMDT)(5)]Cl物种(DMDT = N,N - 二甲基二硫代氨基甲酸盐)的性质进行了比较,其化学(而非生物学)表征已在文献中报道。