Design, synthesis, structural characterization and in vitro cytotoxic activity of mononuclear Ru(II)complexes
作者:Sreekanth Thota、Srujana Vallala、Rajeshwar Yerra、Daniel Alencar Rodrigues、Eliezer J. Barreiro
DOI:10.1007/s00044-016-1625-8
日期:2016.10
The synthesis and characterization of ruthenium complexes (Ru-1–Ru-6) of the type [Ru(R)2(K)]2+ (where R = 1,10-phenanthroline/2,2′-bipyridyl and K = acetyl coumarin-inh, pyrazole-tch, acetyl coumarin-tsz, are described. These ligands form bidentate octahedral ruthenium complexes. The in vitro cytotoxic activities of the complexes measurement against the human cancer T-lymphocyte cell lines. In vitro
[Ru(R)2(K)] 2+类型的钌配合物(Ru-1–Ru-6)的合成与表征(其中R = 1,10-菲咯啉/ 2,2'-联吡啶,K =描述了乙酰香豆素-Inh,吡唑-tch,乙酰香豆素-tsz,这些配体形成了双齿八面体钌配合物,该配合物的体外细胞毒活性对人类癌症T淋巴细胞细胞系的测量,这些标题的体外评估配合物对CEM的细胞毒性为0.34至1.4μg/ mL,对L1210的细胞毒性为0.28至1.8μg/ mL,对Molt4 / C 8为0.44至2.5μg/ mL ,对HL60为0.98至1.6μg/ mL,以及0.66至1.4μg/ mL反对BEL7402。钌配合物Ru-5和Ru-6 结果表明,与标准药物相比,抗癌活性非常重要。