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Synthesis, characterization and cytotoxic activities of the [RuCl2(NO)(dppp)(L)]PF6 complexes

机译:[RuCl2(NO)(dppp)(L)] PF6复合物的合成,表征和细胞毒活性

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The synthesis and characterization of ruthenium compounds of the type [RuCl2(NO)(dppp)(L)]PF6 [dppp = 1,3-bis(diphenylphosphino)propane; L = pyridine, 4-methylpyridine, 4-phenylpyridine and dimethyl sulfoxide] are described. The complexes were characterized by elemental analysis, UV/Vis and infrared spectroscopy, cyclic voltammetry, and X-ray crystallography for the complexes with the pyridine and 4-methylpyridine ligands. In vitro evaluation of these nitrosyl complexes revealed cytotoxic activity from 7.1 to 19.0 lM against the MDA-MB-231 breast tumor cells and showed that, in this case, they are more active than the reference metallodrug cisplatin. The 1,3-bis(diphenylphosphino)propane and the N-heterocyclic ligands alone failed to show cytotoxic activities at the concentrations tested (maximum concentration utilized = 200 lM).
机译:[RuCl2(NO)(dppp)(L)] PF6型钌化合物的合成与表征[dppp = 1,3-双(二苯基膦基)丙烷; L =吡啶,描述了4-甲基吡啶,4-苯基吡啶和二甲基亚砜。通过具有吡啶和4-甲基吡啶配体的配合物的元素分析,UV / Vis和红外光谱,循环伏安法和X射线晶体学表征该配合物。这些亚硝酰基复合物的体外评估显示,其对MDA-MB-231乳腺肿瘤细胞的杀伤活性为7.1至19.0 lM,并显示在这种情况下,它们比参考金属药物顺铂更具活性。单独的1,3-双(二苯基膦基)丙烷和N-杂环配体在所测试的浓度(利用的最大浓度= 200 lM)下未显示出细胞毒活性。

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