Transition metal complexes of phenanthrenequinone thiosemicarbazone as potential anticancer agents: synthesis, structure, spectroscopy, electrochemistry and in vitro anticancer activity against human breast cancer cell-line, T47D

被引:172
作者
Afrasiabi, Z
Sinn, E
Padhye, S
Dutta, S [1 ]
Padhye, S
Newton, C
Anson, CE
Powell, AK
机构
[1] Univ Poona, Dept Chem, Pune 411007, Maharashtra, India
[2] Univ Missouri, Dept Chem, Rolla, MO 65409 USA
[3] Univ Hull, Dept Med Res, Kingston Upon Hull HU6 7RX, N Humberside, England
[4] Univ Karlsruhe, Inst Anorgan Chem, D-76128 Karlsruhe, Germany
关键词
9,10-phenanthrenequinone; thiosemicarbazone; metal complexes; anticancer activity; T47D breast cancer cells;
D O I
10.1016/S0162-0134(03)00131-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The thiosemicarbazone derivative of 9,10-phenanthrenequinone, 1, and its metal complexes were synthesized. The X-ray crystal structure for I confirms the presence of the E tautomeric arrangement in this compound. Its copper complex shows 1: 1 stoichiometry while nickel and cobalt compounds show 1:2 stoichiometry. The X-ray crystal structure of the nickel complex indicates two tridentate ligands coordinating in the thiolato form yielding an octahedral geometry for the 'mer' isomer. The copper complex exhibits maximum antiproliferative activity against human breast cancer cell-line, T47D probably due to inhibition of steroid binding to the cognative receptor or by preventing dimerization of the estrogen receptor. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:306 / 314
页数:9
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