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Structure and biological evaluation of pyridine-2-carboxamidine copper(II) complex resulting from N'-(4-nitrophenylsulfonyloxy)2-pyridine-carboxamidoxime.

Authors :
Perontsis S
Geromichalos GD
Pekou A
Hatzidimitriou AG
Pantazaki A
Fylaktakidou KC
Psomas G
Source :
Journal of inorganic biochemistry [J Inorg Biochem] 2020 Jul; Vol. 208, pp. 111085. Date of Electronic Publication: 2020 Apr 22.
Publication Year :
2020

Abstract

The interaction of Cu(NO <subscript>3</subscript> ) <subscript>2</subscript> ·3H <subscript>2</subscript> O with the sulfonyl o-pyridine carboxamidoxime N'-(4-nitrophenylsulfonyloxy)picolinimidamide (L) resulted in the mononuclear complex [Cu(L <superscript>1</superscript> ) <subscript>2</subscript> ](L <superscript>2</superscript> ) <subscript>2</subscript> (1), where L <superscript>1</superscript>  = pyridine-2-carboxamidine ligand and (L <superscript>2</superscript> ) <superscript>-</superscript> = 4-nitrobenzenesulfonate anion derived from the homolytic cleavage of the NO bond of L. The complex was characterized by diverse techniques including single-crystal X-ray crystallography. From the antimicrobial tests performed, complex 1 seems to be active against gram-negative bacterial strains. The complex binds tightly and reversibly to serum albumins and tightly to calf-thymus DNA via an intercalative mode and also via electrostatic interactions (as expected due to its cationic nature). Additionally, it interacts with (pBluescriptSK(+)) plasmid DNA in a concentration-dependent manner. The results from the present in silico molecular modeling simulations provide useful complementary insights for the elucidation of the mechanism of action of the studied complex at a molecular level. Molecular modeling calculations provide a molecular basis for the understanding of both the impairment of DNA by its binding with the studied complex and the ability of this compound to act as an antibacterial agent, most probably by its activity against DNA-gyrase, as well as for transportation through serum albumins and possible interaction with other protein targets involved in various diseases.<br />Competing Interests: Declaration of competing interest There are no conflicts to declare.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-3344
Volume :
208
Database :
MEDLINE
Journal :
Journal of inorganic biochemistry
Publication Type :
Academic Journal
Accession number :
32454249
Full Text :
https://doi.org/10.1016/j.jinorgbio.2020.111085