首页> 外文期刊>Inorganica Chimica Acta >Characterization, photocleavage, molecular modeling, and DNA- and BSA-binding studies of Cu(II) and Ni(II) complexes with the non-steroidal anti-inflammatory drug meloxicam
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Characterization, photocleavage, molecular modeling, and DNA- and BSA-binding studies of Cu(II) and Ni(II) complexes with the non-steroidal anti-inflammatory drug meloxicam

机译:非甾体类抗炎药美洛昔康对Cu(II)和Ni(II)配合物的表征,光裂解,分子建模以及DNA和BSA结合研究

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摘要

Two complexes of Cu(II) and Ni(II) with the non-steroidal anti-inflammatory drug meloxicam (H(2)mel, 4-hydroxy-2-methyl-N-(5-methyl- 2-thiazolyl)-2H-1,2-benzothiazine-3-carboxammide-1,1-dioxide), trans-[Cu(Hmel)(2)(THF)(2)] (1) and trans-[Ni(Hmel)(2)(DMF)(2)] (2), were synthesized and characterized. The interaction of the complexes with DNA and bovine serum albumin (BSA) was investigated. Molecular docking and molecular dynamic simulation methods were also used for modeling the binding of the complexes to DNA and BSA and good agreements were found between the experimental and theoretical results. All the results suggest that the interaction mode between the complexes and DNA was major groove binding. The quenching mechanism of the BSA fluorescence by the complexes is a static quenching. Gel electrophoresis assay demonstrates the ability of the complexes to cleave the supercoiled plasmid DNA (pUC57 plasmid DNA). (C) 2014 Elsevier B.V. All rights reserved.
机译:Cu(II)和Ni(II)与非甾体抗炎药美洛昔康(H(2)mel,4-hydroxy-2-methyl-N-(5-methyl-2- 2-thiazolyl)-2H -1,2-苯并噻嗪-3-羧酰胺-1,1-二氧化物),反式[Cu(Hmel)(2)(THF)(2)](1)和反式[Ni(Hmel)(2)( DMF)(2)](2)进行了合成和表征。研究了复合物与DNA和牛血清白蛋白(BSA)的相互作用。分子对接和分子动力学模拟方法也被用来模拟复合物与DNA和BSA的结合,并且在实验和理论结果之间找到了很好的一致性。所有结果表明,复合物与DNA之间的相互作用模式是主要的沟结合。配合物对BSA荧光的猝灭机理是静态猝灭。凝胶电泳分析证明了复合物切割超螺旋质粒DNA(pUC57质粒DNA)的能力。 (C)2014 Elsevier B.V.保留所有权利。

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