2017
DOI: 10.3906/kim-1612-53
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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

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 … Show more

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Cited by 6 publications
(2 citation statements)
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“…[1][2][3] They have attracted the attention of researchers because of their biological activities such as anti-microbial, antitumor, anticancer, anti-fungicidal. [4][5][6][7][8][9] Numerous azo compounds are used in pharmaceuticals and cosmetics although some of them have been reported to be toxic. 1 Coordination compounds have also been investigated for the treatment of Alzheimer's disease (AD), Parkinson's dis-ease, aging, and those showing inhibitor activity of AChE promise in the use of therapeutic applications.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…[1][2][3] They have attracted the attention of researchers because of their biological activities such as anti-microbial, antitumor, anticancer, anti-fungicidal. [4][5][6][7][8][9] Numerous azo compounds are used in pharmaceuticals and cosmetics although some of them have been reported to be toxic. 1 Coordination compounds have also been investigated for the treatment of Alzheimer's disease (AD), Parkinson's dis-ease, aging, and those showing inhibitor activity of AChE promise in the use of therapeutic applications.…”
Section: Introductionmentioning
confidence: 99%
“…All chemical and solvents were analytical grade and used without any purification. 2-[(E)-(hydroxyimino) methyl]-4-[(E)-phenyldiazenyl]phenol, H 2 L was prepared according to the reported literature 9.…”
mentioning
confidence: 99%