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dc.contributor.authorKovala-Demertzi, D.en
dc.contributor.authorVidjeluc, C.en
dc.contributor.authorDemertzis, M. A.en
dc.contributor.authorSiapi, E.en
dc.contributor.authorMavromoustakos, T.en
dc.date.accessioned2015-11-24T16:51:14Z-
dc.date.available2015-11-24T16:51:14Z-
dc.identifier.issn0040-6031-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9709-
dc.rightsDefault Licence-
dc.subjectplatinum(ii) and palladium(ii) complexesen
dc.subjectdscen
dc.subjectx-ray structureen
dc.subjectdifferential scanning calorimetryen
dc.subjectcytotoxic activityen
dc.subjectcrystal-structureen
dc.subjectthiosemicarbazoneen
dc.subjectcholesterolen
dc.subjectspectroscopyen
dc.subjecttransitionsen
dc.subjectvinblastineen
dc.subjectderivativesen
dc.subjectpd(ii)en
dc.titleThe thermal effects of platinum(II) and palladium(II) complexes with 2-acetyl pyridine and pyridine-2-carbaldehyde N(4)-ethyl-thiosemicarbazones in membrane bilayersen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1016/j.tca.2004.05.031-
heal.identifier.secondary<Go to ISI>://000224954400007-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0040603104002709/1-s2.0-S0040603104002709-main.pdf?_tid=30478fcc91422592c2f3481f4f999c27&acdnat=1333028846_2806fb40133d1958686a48f564325f33-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2004-
heal.abstractPlatinum(II) and palladium(II) complexes with 2-acetyl pyridine and pyridine-2-carbaidehyde N(4)-ethyl-thiosemicarbazones, HAc4Et and HFo4Et respectively were synthesized and found to exhibit a cytotoxic potency in a very low micromolar range and to be able to overcome the cisplatin resistance of A2780/Cp8 cells. The biologically active complexes Pd(Fo4Et)(2) (1), Pd(Ac4Et)(2) (2), Pt(Fo4Et)(2) (3) and Pt(Ac4Et)(2) (4) were tested for their perturbation in model membrane bilayers. The aim was to investigate if there is a possible relation between their mechanism of action in membranes with their biological activity. Indeed, it was found that complexes of deprotonated HAc4Et, (2) and (4), are more perturbing than complexes of deprotonated HFo4Et, (1) and (3). (C) 2004 Elsevier B.V. All rights reserved.en
heal.journalNameThermochimica Actaen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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