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Title: | 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: | Aliyazicioglu, Yuksel Ayvaz, Melekcol Demir, Selim Dural, Bayram Karaoglu, Kaan Serbest, Kerim Turan, Ibrahim Ordu Üniversitesi 0000-0001-9474-4307 0000-0002-1863-6280 0000-0003-3265-8328 0000-0003-3265-8328 |
Keywords: | Antioxidant activity; bioinorganic chemistry; cytotoxic activity; DNA binding and cleavage activity; topoisomerase inhibitor; transition metal compounds TRANSITION-METAL-COMPLEXES; CANCER-CELL-LINES; TRIDENTATE SCHIFF-BASE; CLEAVAGE ACTIVITY; POLYPYRIDYL COMPLEXES; MACROCYCLIC COMPLEX; BINDING; ACID; DESIGN; MECHANISM |
Issue Date: | 2017 |
Publisher: | SCIENTIFIC TECHNICAL RESEARCH COUNCIL TURKEY-TUBITAK, ATATURK BULVARI NO 221, KAVAKLIDERE, TR-06100 ANKARA, TURKEY |
Abstract: | Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) transition metal complexes of 2-hydroxy-5-[(E)-(4-phenyl) diazenyl] benzaldehyde oxime and 2-hydroxy-5-[(E)-(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 (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 (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. |
URI: | http://doi.org/10.3906/kim-1612-53 https://journals.tubitak.gov.tr/chem/issues/kim-17-41-5/kim-41-5-10-1612-53.pdf http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2575 |
Appears in Collections: | Kimya |
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