2015
DOI: 10.1039/c4ra16484a
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Copper(ii) complexes of salicylaldehydes and 2-hydroxyphenones: synthesis, structure, thermal decomposition study and interaction with calf-thymus DNA and albumins

Abstract: The characterized copper(ii) complexes with substituted salicylaldehydes and 2-hydroxyphenones exhibit enhanced affinity for DNA and albumins in comparison to free ligands.

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Cited by 43 publications
(13 citation statements)
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“…Our interest is based on the synthesis of metal complexes with substituted salicylaldehydes and their interaction with DNA. Previous studies showed that zinc(II) and copper(II) complexes with substituted salicylaldehydes or 2-hydroxybenzophenones have interesting binding to calf-thymus (CT) DNA [32,33,35], while Co(II) complexes in the presence of the nitrogen-donor ligand 2,2'-dipyridylamine (dpamH) exhibited anticancer activity [31].…”
mentioning
confidence: 99%
“…Our interest is based on the synthesis of metal complexes with substituted salicylaldehydes and their interaction with DNA. Previous studies showed that zinc(II) and copper(II) complexes with substituted salicylaldehydes or 2-hydroxybenzophenones have interesting binding to calf-thymus (CT) DNA [32,33,35], while Co(II) complexes in the presence of the nitrogen-donor ligand 2,2'-dipyridylamine (dpamH) exhibited anticancer activity [31].…”
mentioning
confidence: 99%
“…8). [30,31] It was confirmed the addition of Cu 2+ results electron transfer redox (oxidation-reduction) process. The anodic peaks for 4MHEB-Cu 2+ ion appeared at Epa = -0.0242 V and cathodic peak Epc = +0.3027 V while anodic peak at Epa = -0.1470 V and cathodic peak Epc = +0.5890 V for 4MHEB.…”
Section: Cyclic Voltammetric Studymentioning
confidence: 80%
“…In pursuit of developing better copper based anti-inflammatory drugs which can be administered orally, intravenously or even transdermally, they have designed and synthesized two ligands, N, NO-di (aminoethylene)-2,6pyridinedicarbonylamine (L1) and bis-(N, Ndimethylethyl)-2,6-pyridinedicarboxamide (L2). L1 and L2 both have pyridyl groups which are found in most of the non-steroidal anti-inflammatory drugs (NSAIDs) [48]. A class of quinoline based compounds has been explored and found to have the ability to inhibit platelet-activating factor (PAF) synthesis which also contributes to antiinflammatory properties [49].…”
Section: Anti-inflammatory Agentsmentioning
confidence: 99%