Platinum(IV) complexes with ethylenediamine-N,N′-diacetate diester (R₂edda) ligands: Synthesis, characterization and in vitro antitumoral activity

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• 作者：Goran N. Kaluđ ; erović ; Harry Schmidt ; Sebastian Schwieger ; Christoph Wagner ; Reinhard Paschke ; Andrea Dietrich ; Thomas Mueller ; Dirk Steinborn
• 关键词：Platinum(IV) complexes ; Edda ligand ; Antiproliferative activity ; Crystal structure ; DFT
• 刊名：Inorganica Chimica Acta
• 出版年：2008
• 期刊代码：40_00201693
• 类别：ch
• 出版时间：1 April 2008
• 卷：361
• 期：5
• 页码：1395-1404
• 文件大小：492 K

摘要

The novel N,N-type bidentate ligand precursors, diethyl, dipropyl esters of ethylenediamine-N,N′-diacetic acid dihydrochloride (HOOCCH₂NHCH₂CH₂NHCH₂COOH · 2HCl, H₂edda · 2HCl), and the corresponding tetrachloroplatinum(IV) complexes, [PtCl₄(R₂edda)] · H₂O (ROOCCH₂NHCH₂CH₂NHCH₂COOR, R = Me, Et, n-Pr), were synthesized. The esters coordinated as bidentate ligands via both N donor atoms. The esters, as well as the complexes, have been characterized by infrared, ¹H and ¹³C NMR spectroscopy and elemental analysis. Solid state structures of both dimethyl and diethyl ester platinum(IV) complexes have been determined by X-ray crystallography. Quantum chemical calculations were performed in order to investigate diastereoselectivity in the formation of the platinum(IV) complexes. The in vitro cytotoxic evaluation of the investigated complexes in human tumor cell lines 1411HP, H12.1 (both testicular germ cell tumors), DLD-1 (colon carcinoma), 518A2 (melanoma), A549 (lung carcinoma) and liposarcoma showed a dose-dependent antiproliferative effect in all cell lines. Remarkably, the highest cytotoxic activity was observed in the cisplatin-resistant cell line 1411HP. In addition, at higher concentrations the treatment with these complexes led to the induction of apoptosis in all cell lines except for DLD-1.