Synthesis, crystal and electronic structure, anticancer activity of ruthenium(II) arene complexes with thiosemicarbazones

被引:32
作者
Su, Wei [1 ]
Zhou, Quan [1 ]
Huang, Yanmin [1 ]
Huang, Qianyang [1 ]
Huo, Lini [2 ]
Xiao, Qi [1 ]
Huang, Shan [1 ]
Huang, Chusheng [1 ]
Chen, Rui [2 ]
Qian, Quanquan [1 ]
Liu, Lifeng [1 ]
Li, Peiyuan
机构
[1] Guangxi Teachers Educ Univ, Coll Chem & Life Sci, Nanning 530001, Peoples R China
[2] Guangxi Univ Chinese Med, Coll Pharm, Nanning 530001, Peoples R China
基金
中国国家自然科学基金;
关键词
ruthenium complexes; thiosemicarbazones ligand; anticancer research; DFT and TDDFT calculated; IN-VITRO;
D O I
10.1002/aoc.2977
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of half-sandwich ruthenium(II) arene complexes [(6-p-cymene)RuII(R-BzTSC)Cl]Cl (BzTSC=benzaldehyde thiosemicarbazone and R=H, CH3 and C6H5) have been synthesized and characterized by IR, 1H NMR, UV-visible, electrospray ionization mass spectrometry and elemental analysis. The single-crystal structures of and have been determined. The molecular orbitals and electronic absorption spectra of the compounds have been calculated using the DFT and TDDFT methods. The in vitro antiproliferative activities of these complexes have been evaluated against four human cancer cell lines (CNE, H292, SKBR3 and Hey1-B), and is proved to be the most efficient inhibitor, with IC50 values of 20, 31, 10 and 34 m, respectively. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:307 / 312
页数:6
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