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dc.creatorLeovac, Vukadin M.
dc.creatorBogdanović, Goran A.
dc.creatorJovanović, Ljiljana S.
dc.creatorJoksović, Ljubinka
dc.creatorMarković, Violeta
dc.creatorJoksović, Milan D.
dc.creatorMisirlic-Dencić, Sonja
dc.creatorIsaković, Anđelka
dc.creatorMarković, Ivanka
dc.creatorHeinemann, Frank W.
dc.creatorTrifunović, Srećko R.
dc.creatorĐalović, Ivica
dc.date.accessioned2021-04-26T18:51:09Z
dc.date.available2021-04-26T18:51:09Z
dc.date.issued2011
dc.identifier.issn0162-0134
dc.identifier.urihttp://fiver.ifvcns.rs/handle/123456789/1018
dc.description.abstractNew polymeric copper(II) complexes with two tridentate ONS thiosemicarbazone ligands containing substituted pyrazolone moiety were synthesized and characterized by means of spectroscopic, electrochemical and crystallographic techniques. While both ligands exist as different tautomers in the solid state and DMSO-d(6) solution, Cu(II) ion coordinates the ligands from the same tautomeric form with square-pyramidal geometry around each Cu atom. In the crystal structures, the copper(II) complex cation forms polymeric chains {[Cu(L)Cl+]}(n) with a bridging chlorine atom. One of the complexes was found to have a significantly higher cytotoxic potential in comparison with cisplatin in inhibition of several cell lines (HL60, REH, C6, L929 and B16). The results obtained on the basis of flow cytometry indicated that apoptosis could be possible mechanism of cell death.en
dc.publisherElsevier Science Inc, New York
dc.relationProvincial Secretariat for Science and Technological Development, Autonomous Province of Vojvodina, Republic of Serbia
dc.rightsrestrictedAccess
dc.sourceJournal of Inorganic Biochemistry
dc.subjectCopper(II) complexesen
dc.subjectPyrazoloneen
dc.subjectThiosemicarbazoneen
dc.subjectX-ray structuresen
dc.subjectElectrochemistryen
dc.subjectCytotoxicityen
dc.titleSynthesis, characterization and antitumor activity of polymeric copper(II) complexes with thiosemicarbazones of 3-methyl-5-oxo-1-phenyl-3-pyrazolin-4-carboxaldehyde and 5-oxo-3-phenyl-3-pyrazolin-4-carboxaldehydeen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage1421
dc.citation.issue11
dc.citation.other105(11): 1413-1421
dc.citation.rankM21
dc.citation.spage1413
dc.citation.volume105
dc.identifier.doi10.1016/j.jinorgbio.2011.07.021
dc.identifier.pmid21955843
dc.identifier.scopus2-s2.0-80053348340
dc.identifier.wos000297565500007
dc.type.versionpublishedVersion


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Приказ основних података о документу