Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10932
Title: Interactions of zinc(II) complexes with 5′-GMP and their cytotoxic activity
Authors: V. Soldatovic, Tanja
Selimovic, Enisa
Šmit, Biljana
Ašanin, Darko
Planojević, Nina
Marković, Snežana
Puchta, Ralph
Alzoubi, Basam
Journal: Journal of Coordination Chemistry
Issue Date: 16-Feb-2019
Abstract: © 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group. The mechanism of substitution from tetrahedral [ZnCl 2 (en)] and square-pyramidal [ZnCl 2 (terpy)] complexes (where en = 1,2-diaminoethane or ethylenediamine and terpy = 2,2′:6′,2′′-terpyridine) by guanosine-5′-monophosphate (5′-GMP) have been investigated by 1 H NMR spectroscopy. The substitution reaction of [ZnCl 2 (terpy)] complex is faster than the reaction of [ZnCl 2 (en)], which was finished after 48 h. Information about the structures of the final products in solution were obtained from the DFT calculations (B3LYP/6-31G(d)) and experimental 1 H NMR data acquired during the course of the reaction. The cytotoxic activity of zinc(II) complexes was tested on human breast cancer cell line MDA-MB-231, human colon cancer cell line HCT-116 and normal human lung fibroblast cell line MRC-5. Both complexes reduced cell viabilities, while [ZnCl 2 (terpy)] was significantly cytotoxic on MDA-MB-231 after 72 h, and HCT-116 after 24 h without dose dependence. The differences in reactivity toward 5′-GMP and cytotoxic activity of Zn(II) complexes may be attributed to the very stable square-pyramidal geometry of [ZnCl 2 (terpy)] in solution, while weak ligand effect of the en compared to the terpy affected slow interaction of tetrahedral [ZnCl 2 (en)] complex with the target bio-molecule.
URI: https://scidar.kg.ac.rs/handle/123456789/10932
Type: Article
DOI: 10.1080/00958972.2019.1569229
ISSN: 00958972
SCOPUS: 85061075764
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac
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