Antiproliferative Copper(II) and Platinum(II) Complexes with Bidentate N,N-Donor Ligands

被引:12
|
作者
Sommerfeld, Nadine S. [1 ]
Guelzow, Jana [2 ]
Roller, Alexander [1 ]
Cseh, Klaudia [1 ]
Jakupec, Michael A. [1 ,3 ]
Grohmann, Andreas [2 ]
Galanski, Markus [1 ]
Keppler, Bernhard K. [1 ,3 ]
机构
[1] Univ Vienna, Inst Inorgan Chem, Waehringer Str 42, A-1090 Vienna, Austria
[2] Berlin Univ Technol, Inst Chem, Str 17 Juni 135, D-10623 Berlin, Germany
[3] Univ Vienna, Res Cluster Translat Canc Therapy Res, Waehringer Str 42, A-1090 Vienna, Austria
关键词
Platinum; Copper; Antiproliferation; Cytotoxicity; Anticancer agents; CONTINUOUS SYMMETRY MEASURES; STRUCTURAL-CHARACTERIZATION; ANTICANCER AGENTS; IN-VITRO; CELLS; CU(II); DNA; CASIOPEINAS(R); INDUCTION; APOPTOSIS;
D O I
10.1002/ejic.201700416
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three copper(II) complexes of a series of bidentate dipyridylmethane ligands, as well as their structurally related platinum(II) analogues, have been synthesised and fully characterised to evaluate their coordination chemistry and antiproliferative properties. New crystal structures of the complexes (LCuCl2)-Cu-3, (LPtCl2)-Pt-2 and (LPtCL2)-Pt-3, where L-2, L-3 have one and two methyl substituents on the bridgehead carbon atom between the coordinated pyridine ligands, respectively, were obtained. The in vitro cytotoxicity of the free ligands and their corresponding platinum and copper complexes was evaluated in the cisplatin-sensitive ovarian teratocarcinoma cell line CH1/PA1, as well as in rather cisplatin-insensitive colon (SW480) and lung (A549) carcinoma cells, using the MTT assay. All six complexes showed higher cytotoxicity than the ligands L-1-L-3 alone, giving IC50 values in the low micromolar range.
引用
收藏
页码:3115 / 3124
页数:10
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