Centro de Química Estrutural, Complexo I, Instituto Superior Técnico, Technical University of Lisbon, Av. Rovisco Pais, 1049-001 Lisboa, Portugal.
Dalton Trans. 2012 Nov 7;41(41):12888-97. doi: 10.1039/c2dt11577h.
A number of novel, water-stable redox-active cobalt complexes of the C-functionalized tripodal ligands tris(pyrazolyl)methane XC(pz)(3) (X = HOCH(2), CH(2)OCH(2)Py or CH(2)OSO(2)Me) are reported along with their effects on DNA. The compounds were isolated as air-stable solids and fully characterized by IR and FIR spectroscopies, ESI-MS(+/-), cyclic voltammetry, controlled potential electrolysis, elemental analysis and, in a number of cases, also by single-crystal X-ray diffraction. They showed moderate cytotoxicity in vitro towards HCT116 colorectal carcinoma and HepG2 hepatocellular carcinoma human cancer cell lines. This viability loss is correlated with an increase of tumour cell lines apoptosis. Reactivity studies with biomolecules, such as reducing agents, H(2)O(2), plasmid DNA and UV-visible titrations were also performed to provide tentative insights into the mode of action of the complexes. Incubation of Co(II) complexes with pDNA induced double strand breaks, without requiring the presence of any activator. This pDNA cleavage appears to be mediated by O-centred radical species.
报道了一系列新型的、水稳定的氧化还原活性钴配合物,这些配合物是基于 C 功能化的三脚架配体三(吡唑基)甲烷 XC(pz)(3)(X = HOCH(2),CH(2)OCH(2)Py 或 CH(2)OSO(2)Me)合成的,同时还研究了它们对 DNA 的影响。这些化合物作为空气稳定的固体被分离出来,并通过红外和远红外光谱、ESI-MS(+/-)、循环伏安法、恒电位电解、元素分析以及在许多情况下还通过单晶 X 射线衍射进行了全面表征。它们对 HCT116 结直肠癌和 HepG2 肝癌人癌细胞系表现出中等的体外细胞毒性。这种活力丧失与肿瘤细胞系凋亡的增加有关。还进行了与生物分子(如还原剂、H(2)O(2)、质粒 DNA 和紫外可见滴定)的反应性研究,以提供对配合物作用模式的初步见解。Co(II)配合物与 pDNA 的孵育诱导了双链断裂,而不需要任何激活剂的存在。这种 pDNA 切割似乎是由 O 中心自由基物种介导的。