Metal N-heterocyclic carbene complexes as potential antitumor metallodrugs

被引:666
作者
Liu, Wukun [1 ]
Gust, Ronald [1 ,2 ]
机构
[1] Free Univ Berlin, Inst Pharm, D-14195 Berlin, Germany
[2] Univ Innsbruck, Inst Pharm, Dept Pharmaceut Chem, Ctr Mol Biosci Innsbruck,CCB, A-6020 Innsbruck, Austria
关键词
THIOREDOXIN REDUCTASE INHIBITION; PLATINUM ANTICANCER COMPLEX; INTERSTRAND CROSS-LINKS; IN-VITRO; GOLD(I) COMPLEXES; SILVER COMPLEXES; ORGANOMETALLIC CHEMISTRY; THERAPEUTIC APPLICATIONS; MOLECULAR-MECHANISMS; PHOSPHINE COMPLEXES;
D O I
10.1039/c2cs35314h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The discovery of cisplatin's antitumor activity in 1969 prompted the search for novel metal-containing complexes as potential anticancer drugs. Among these novel complexes, metal N-heterocyclic carbene (NHC) complexes have recently gained considerable attention because they perfectly fit prerequisites for efficient drug design and fast optimization. Moreover, most of them have shown higher cytotoxicity than cisplatin. This review describes the advances that have been achieved in using transition metal (Ag, Au, Pt, Pd, Cu, Ni, and Ru) complexes containing NHC ligands as antitumor agents. Their modes of action at the cellular lever are further discussed. All these initial achievements clearly demonstrate the great potential of metal-NHC complexes as antitumor agents.
引用
收藏
页码:755 / 773
页数:19
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