Advances in Copper Complexes as Anticancer Agents

被引:1540
作者
Santini, Carlo [1 ]
Pellei, Maura [1 ]
Gandin, Valentina [2 ]
Porchia, Marina [3 ]
Tisato, Francesco [3 ]
Marzano, Cristina [2 ]
机构
[1] Univ Camerino, Scuola Sci & Tecnol Sez Chim, I-62032 Camerino, Macerata, Italy
[2] Univ Padua, Dipartimento Sci Farmaco, I-35131 Padua, Italy
[3] IENI CNR, I-35127 Padua, Italy
关键词
IN-VITRO CYTOTOXICITY; DNA-BINDING PROPERTIES; TOPOISOMERASE-II-ALPHA; METAL ION COMPLEXES; CELL-CYCLE ARREST; APOPTOSIS-INDUCING ACTIVITIES; SELECTIVE ANTITUMOR-ACTIVITY; EHRLICH ASCITES-CARCINOMA; PHOSPHATASE-LIKE ACTIVITY; MIXED-LIGAND COMPLEXES;
D O I
10.1021/cr400135x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The research on copper(I,II) coordination compounds as antiproliferative agents has increased as demonstrated by the high number of papers published in this field in the period 2008-2012. The first consideration which stems from the presented data concerns the large variety of ligands used to synthesize potentially active copper drugs. The reported copper complexes (mostly copper(II)) comprised ligands of different hapticity, from monodentate to hexadentate, and characterized by different donor atoms (O, N, S, P, and C) which gave rise to different geometrical arrangements and, in some cases, dimeric and polymeric species. Regarding the copper oxidation state, there is no direct correlation between the antiproliferative activity and reduced or oxidized forms of the metal. However, the few reported copper(I) complexes, featured by phosphine or heterocyclic carbene ligands generally showed a potent cytotoxic activity. Most of the studies with copper complexes continue to consider DNA as the main biological target.
引用
收藏
页码:815 / 862
页数:48
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