Synthesis, characterization and antiproliferative activity of platinum(II) complexes with 3-(2-pyridyl)-N1,2-methyl-1,2,4-triazoles

被引:5
作者
Ohorodnik, Yulia M. [1 ]
Khomenko, Dmytro M. [1 ,2 ]
Doroshchuk, Roman O. [1 ,2 ]
Raspertova, Ilona, V [1 ]
Shova, Sergiu [3 ]
Babak, Maria, V [4 ]
Milunovic, Miljan N. M. [5 ]
Lampeka, Rostyslav D. [1 ]
机构
[1] Kyiv Natl Taras Shevchenko Univ, Dept Chem, Volodymyrska St 64, Kiev, Ukraine
[2] Enamine Ltd, Chervonotkatska St 78, UA-02094 Kiev, Ukraine
[3] Petru Poni Inst Macromol Chem, Aleea Gr Gh Voda 41A, Iasi 700487, Romania
[4] City Univ Hong Kong, Dept Chem, Drug Discovery Lab, 83 Tat Chee Ave, Hong Kong 999077, Peoples R China
[5] Univ Vienna, Inst Inorgan Chem, Fac Chem, Wahringer Str 42, A-1090 Vienna, Austria
关键词
1; 2; 4-Triazole; Platinum; NMR-spectroscopy; Cisplatin; Crystal structures; PALLADIUM(II) COMPLEXES; ANTICANCER; PYRIDINE; LIGANDS; DESIGN; DMSO;
D O I
10.1016/j.ica.2023.121646
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The present work describes the synthesis, investigation and in vitro cytotoxicity of Pt(II) complexes with 3-(2pyridyl)-N1-methyl-1,2,4-triazole (L1) and 3-(2-pyridyl)-N2-methyl-1,2,4-triazole (L2). The crystal structures of PtL1Cl2 and PtL2Cl2 were established using X-Ray analysis, which revealed the square-planar PtN2Cl2 coordination geometry for the central metal ion. High-resolution mass spectrometry (HRMS), as well as one-and twodimensional nuclear magnetic resonance (NMR) spectroscopy showed stability of the investigated complexes in DMF solution, in contrast to DMSO, where species were shown to partially dissociate. The cytotoxicity of the investigated compounds was determined by the colorimetric MTT assay against two human cancer cell lines, including cisplatin-sensitive human ovarian adenocarcinoma A2780 cells (IC50 = 26 & PLUSMN; 5 and 6.1 & PLUSMN; 0.6 for PtL1Cl2 and PtL2Cl2 correspondingly) and their cisplatin-resistant A2780cis analogue (IC50 = 24 & PLUSMN; 2 and 20 & PLUSMN; 3 for PtL1Cl2 and PtL2Cl2 correspondingly).
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页数:7
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