Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29450
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dc.contributor.authorHarrison, William T. A.-
dc.date.accessioned2022-11-11T07:07:25Z-
dc.date.available2022-11-11T07:07:25Z-
dc.date.issued2013-02-
dc.identifier.citationİçsel, C. vd. (2013). "Trans-Dichloridopalladium(II) and platinum(II) complexes with 2-(hydroxymethyl)pyridine and 2-(2-hydroxyethyl)pyridine: Synthesis, structural characterization, DNA binding and in vitro cytotoxicity studies". European Journal of Medicinal Chemistry, 60, 386-394 .en_US
dc.identifier.issn0223-5234-
dc.identifier.issn1768-3254-
dc.identifier.urihttps://doi.org/10.1016/j.ejmech.2012.12.002-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0223523412007246-
dc.identifier.urihttp://hdl.handle.net/11452/29450-
dc.description.abstractFour trans-palladium(II)- and trans-platinum(II)-chlorido complexes, trans-[PdCl2(2-hmpy)(2)] (1), trans-[PtCl2(2-hmpy)(2)] (2), trans-[Pdcl(2)(2-hepy)(2)] (3) and trans-[PtCl2(2-hepy)(2)] (4) (2-hmpy = 2-(hydroxymethyl)pyridine and 2-hepy = 2-(2-hydroxyethyl)pyridine), have been synthesized and characterized by elemental analysis, IR, NMR, and X-ray diffraction. The binding properties of these complexes with fish sperm DNA (FS-DNA) were investigated by UV titration, viscosity, thermal denaturation and electrophoresis measurements. The complexes can bind to FS-DNA and complex 4 exhibits the highest binding constant. Gel electrophoresis assay demonstrates that all the complexes can cleave the pCMV-beta gal plasmid DNA to a different degree. The cytotoxic activities of the complexes were tested against four different cancer cell lines. In general, the platinum(II) complexes are more effective than the isostructural palladium(II) complexes. Complex 4 shows high anticancer activity, compared to transplatin, cisplatin, carboplatin and oxaliplatin.en_US
dc.language.isoenen_US
dc.publisherElsevier Franceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPharmacology & pharmacyen_US
dc.subjectTransplatinum complexesen_US
dc.subject2-(Hydroxymethyl)pyridineen_US
dc.subject2-(2-Hydroxyethyl)pyridineen_US
dc.subjectDNA bindingen_US
dc.subjectCytotoxic activityen_US
dc.subjectTrans geometryen_US
dc.subjectEthidium-bromideen_US
dc.subjectMetal-complexesen_US
dc.subjectAntitumoren_US
dc.subjectPalladium(II)en_US
dc.subjectPd(II)en_US
dc.subjectLiganden_US
dc.subjectDrugsen_US
dc.subjectRuthenium(II)en_US
dc.subjectFluorescenceen_US
dc.subject.meshAnimalsen_US
dc.subject.meshAntineoplastic agentsen_US
dc.subject.meshBinding sitesen_US
dc.subject.meshCell line, tumoren_US
dc.subject.meshCell proliferationen_US
dc.subject.meshCHO cellsen_US
dc.subject.meshCricetinaeen_US
dc.subject.meshDNAen_US
dc.subject.meshDose-response relationship, drugen_US
dc.subject.meshDrug screening assays, antitumoren_US
dc.subject.meshHumansen_US
dc.subject.meshMolecular structureen_US
dc.subject.meshOrganoplatinum compoundsen_US
dc.subject.meshPalladiumen_US
dc.subject.meshPlatinumen_US
dc.subject.meshPyridinesen_US
dc.subject.meshRatsen_US
dc.subject.meshStructure-activity relationshipen_US
dc.titleTrans-Dichloridopalladium(II) and platinum(II) complexes with 2-(hydroxymethyl)pyridine and 2-(2-hydroxyethyl)pyridine: Synthesis, structural characterization, DNA binding and in vitro cytotoxicity studiesen_US
dc.typeArticleen_US
dc.identifier.wos000316242700039tr_TR
dc.identifier.scopus2-s2.0-84872160407tr_TR
dc.relation.tubitak111T099tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-6729-7908tr_TR
dc.contributor.orcid0000-0002-2849-3332tr_TR
dc.contributor.orcid0000-0002-2717-2430tr_TR
dc.identifier.startpage386tr_TR
dc.identifier.endpage394tr_TR
dc.identifier.volume60tr_TR
dc.relation.journalEuropean Journal of Medicinal Chemistryen_US
dc.contributor.buuauthorİçsel, Ceyda-
dc.contributor.buuauthorYılmaz, Veysel T.-
dc.contributor.buuauthorArı, Ferda-
dc.contributor.buuauthorUlukaya, Engin-
dc.contributor.researcheridAAG-7012-2021tr_TR
dc.contributor.researcheridL-7238-2018tr_TR
dc.contributor.researcheridK-5792-2018tr_TR
dc.contributor.researcheridAAI-3342-2021tr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.identifier.pubmed23314052tr_TR
dc.subject.wosChemistry, medicinalen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ1en_US
dc.contributor.scopusid55551960400tr_TR
dc.contributor.scopusid7006269202tr_TR
dc.contributor.scopusid24376085300tr_TR
dc.contributor.scopusid6602927353tr_TR
dc.subject.scopusAntineoplastic Activity; Prodrugs; Transplatinen_US
dc.subject.emtreeCisplatinen_US
dc.subject.emtreeDNAen_US
dc.subject.emtreePalladium complexen_US
dc.subject.emtreePlasmid DNAen_US
dc.subject.emtreePlatinum complexen_US
dc.subject.emtreePyridine derivativeen_US
dc.subject.emtreeTransplatinen_US
dc.subject.emtreeAbsorption spectroscopyen_US
dc.subject.emtreeAnimal cellen_US
dc.subject.emtreeAntineoplastic activityen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCancer cellen_US
dc.subject.emtreeCancer cell cultureen_US
dc.subject.emtreeCarbon nuclear magnetic resonanceen_US
dc.subject.emtreeCell viabilityen_US
dc.subject.emtreeColon canceren_US
dc.subject.emtreeConcentration responseen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeCrystal structureen_US
dc.subject.emtreeCytotoxicityen_US
dc.subject.emtreeDNA bindingen_US
dc.subject.emtreeDNA denaturationen_US
dc.subject.emtreeDrug synthesisen_US
dc.subject.emtreeFibroblasten_US
dc.subject.emtreeGel electrophoresisen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeIn vitro studyen_US
dc.subject.emtreeInfrared spectrophotometryen_US
dc.subject.emtreeInteractions with DNAen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreeRaten_US
dc.subject.emtreeStructure analysisen_US
dc.subject.emtreeTitrimetryen_US
dc.subject.emtreeUltraviolet radiationen_US
dc.subject.emtreeViscosityen_US
dc.subject.emtreeX ray diffractionen_US
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