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  • Turkish Journal of Chemistry
  • Volume:41 Issue:5
  • Synthesis, in vitro DNA interactions, cytotoxicities, antioxidative activities, and topoisomerase in...

Synthesis, in vitro DNA interactions, cytotoxicities, antioxidative activities, and topoisomerase inhibition potentials of Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) complexes with azo-oxime ligands

Authors : Melek Çol AYVAZ, İbrahim TURAN, Bayram DURAL, Selim DEMİR, Kaan KARAOĞLU, Yüksel ALİYAZICIOĞLU, Kerim SERBEST
Pages : 728-747
View : 22 | Download : 12
Publication Date : 0000-00-00
Article Type : Research Paper
Abstract :Mninsert ignore into journalissuearticles values(II);, Coinsert ignore into journalissuearticles values(II);, Niinsert ignore into journalissuearticles values(II);, Cuinsert ignore into journalissuearticles values(II);, and Zninsert ignore into journalissuearticles values(II); transition metal complexes of 2-hydroxy-5-[insert ignore into journalissuearticles values(E);-insert ignore into journalissuearticles values(4-phenyl); diazenyl] benzaldehyde oxime and 2-hydroxy-5-[insert ignore into journalissuearticles values(E);-insert ignore into journalissuearticles values(4-nitrophenyl); diazenyl] benzaldehyde oxime ligands were synthesized and characterized through NMR, IR, ESI mass, and UV analysis. DNA binding abilities of the complexes were revealed using a UV-Vis spectrophotometer with the absorption titration and competitive binding techniques. Hydrolytic and oxidative DNA cleavage activities under different conditions were also proved. Topoisomerase I inhibition efficiencies and in vitro free radical scavenging activities of all complexes were examined. Finally, the selective cytotoxic potentials of all complexes were evaluated in human colon cancer, normal colon, and fibroblast cell lines using the water-soluble tetrazolium salt insert ignore into journalissuearticles values(WST-1); assay. The complexes had the ability to intercalate into stacked base pairs of DNA and topoisomerase I activity was reasonably inhibited in their presence in 0.4 mM concentrations. The abilities for scavenging of DPPH and hydroxyl radicals were found to be higher than those of known standard antioxidants insert ignore into journalissuearticles values(ascorbic acid, butylated hydroxyanisole, and mannitol);. The results obtained from the cytotoxicity experiments are especially promising for further research, which must be carried out for the evaluation of the studied complexes as anticancer drugs.
Keywords : Antioxidant activity, bioinorganic chemistry, cytotoxic activity, DNA binding and cleavage activity, topoisomerase inhibitor, transition metal compounds

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