School of Chemical Science, The University of Auckland Auckland, New Zealand ; Institute of Inorganic Chemistry, University of Vienna Vienna, Austria ; Department of Chemistry, COMSATS Institute of Information Technology Abbottabad, Pakistan.
Institute of Inorganic Chemistry, University of Vienna Vienna, Austria ; Research Platform "Translational Cancer Therapy Research", University of Vienna Vienna, Austria.
Front Chem. 2013 Oct 31;1:27. doi: 10.3389/fchem.2013.00027. eCollection 2013.
The synthesis and in vitro cytotoxicity of a series of Ru(II)(arene) complexes with carbohydrate-derived phosphite ligands and various arene co-ligands is described. The arene ligand has a strong influence on the in vitro anticancer activity of this series of compounds, which correlates fairly well with cellular accumulation. The most lipophilic compound bearing a biphenyl moiety and a cyclohexylidene-protected carbohydrate is the most cytotoxic with unprecedented IC50 values for the compound class in three human cancer cell lines. This compound shows reactivity to the DNA model nucleobase 9-ethylguanine, but does not alter the secondary structure of plasmid DNA, indicating that other biological targets are responsible for its cytotoxic effect.
本文描述了一系列具有碳水化合物衍生膦酸酯配体和各种芳族共配体的 Ru(II)(芳基)配合物的合成和体外细胞毒性。芳族配体对这一系列化合物的体外抗癌活性有很强的影响,与细胞积累相关性较好。带有联苯部分和环己基亚甲基保护的碳水化合物的最亲脂性化合物具有最高的细胞毒性,在三种人癌细胞系中具有前所未有的 IC50 值。该化合物对 DNA 模型碱基 9-乙基鸟嘌呤具有反应性,但不改变质粒 DNA 的二级结构,表明其他生物靶标是其细胞毒性作用的原因。