Binuclear copper(II) complexes of tolfenamic: synthesis, crystal structure, spectroscopy and superoxide dismutase activity

dc.contributor.authorKovala-Demertzi, D.en
dc.contributor.authorGalani, A.en
dc.contributor.authorDemertzis, M. A.en
dc.contributor.authorSkoulika, S.en
dc.contributor.authorKotoglou, C.en
dc.date.accessioned2015-11-24T16:53:05Z
dc.date.available2015-11-24T16:53:05Z
dc.identifier.issn0162-0134-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9969
dc.rightsDefault Licence-
dc.subjectnsaidsen
dc.subjecttolfenamicen
dc.subjectcrystal structureen
dc.subjectspectroscopic studyen
dc.subjectsod mimeticen
dc.subjectmetal-complexesen
dc.subjectantiinflammatory propertiesen
dc.subjectaciden
dc.subjectdiclofenacen
dc.titleBinuclear copper(II) complexes of tolfenamic: synthesis, crystal structure, spectroscopy and superoxide dismutase activityen
heal.abstractThe synthesis and characterization of copper(II) complexes with a potent non-steroidal anti-inflammatory drug, tolfenamic acid, Htolf, with formula [Cu(tolf)(2)L](2) (where L is H2O or DMF, N,N-dimethylformamide) were investigated. The crystal-and molecular structure Of [Cu(tolf)(2)(DMF)](2) was reported. Crystallographic data are as follows: monoclinic system, space group P2(1)/n with cell constants a = 9.068(2) Angstrom, b = 14.514(3) Angstrom, c = 22.826(4) Angstrom, V = 2948.9(10) Angstrom(3) and Z = 2. The crystal structure consists of binuclear, quadruply bridged neutral molecule with a Cu-Cu bond length of 2.6075(19) Angstrom. The complex is self-assembled via C-H-pi intermolecular stacking interactions. Spectroscopic and electrochemical studies were reported. The superoxide dismutase activity is measured and compared with those of superoxide dismutase enzyme, SOD, the free ligand and related copper complexes with nonsteroidal anti-inflammatory drugs, NSAIDs. IC50 value was measured by the Fridovich test (1.97 +/- 0.17 muM), which showed that [Cu(tolf)(2)L](2) is a good superoxide scavenger. (C) 2003 Elsevier Inc. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.jinorgbio.2003.11.004-
heal.identifier.secondary<Go to ISI>://000188711200018-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0162013403004410/1-s2.0-S0162013403004410-main.pdf?_tid=2a130c5fa8aa1e8ce0187e8622ce0995&acdnat=1333028827_8a54671ff3d9941a1d1f2789002e8531-
heal.journalNameJ Inorg Biochemen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2004-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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