Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29461
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dc.contributor.authorGölcü, Ayşegül-
dc.contributor.authorBüyukgüngör, Orhan-
dc.date.accessioned2022-11-16T13:18:54Z-
dc.date.available2022-11-16T13:18:54Z-
dc.date.issued2013-04-
dc.identifier.citationİçsel, C. vd. (2013). "Synthesis, crystal structures, DNA binding and cytotoxicity of two novel platinum(II) complexes containing 2-(hydroxymethyl)pyridine and pyridine-2-carboxylate ligands". Bioorganic and Medicinal Chemistry Letters, 23(7), 2117-2122.en_US
dc.identifier.issn0960-894X-
dc.identifier.issn1464-3405-
dc.identifier.urihttps://doi.org/10.1016/j.bmcl.2013.01.119-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0960894X13001522-
dc.identifier.urihttp://hdl.handle.net/11452/29461-
dc.description.abstractTwo new platinum(II) complexes, trans-[Pt(2-mpy)(2)]center dot 4H(2)O (1) and [PtCl(2-pyc)(2-hmpy)]center dot H2O (2), where 2-hmpy = 2-(hydroxymethyl)pyridine, 2-mpy = deprotonated 2-hmpy and 2-pyc = pyridine-2-carboxylate, have been synthesized and characterized by elemental analysis, IR, NMR, and X-ray crystallography. The DNA binding affinities of these complexes for Fish Sperm DNA (FS-DNA) were investigated using fluorescence, viscosity, thermal denaturation and gel electrophoresis measurements. Fluorescence analysis indicates that complex 1 binds to DNA by a single intercalative mechanism, while complex 2 exhibits two types of interactions such as intercalation and covalent binding. Gel electrophoresis assay demonstrates ability of the complexes to cleavage the supercoiled 0311322 plasmid DNA. The in vitro cytotoxicities of both complexes were preliminarily evaluated and the cytotoxicity of complex 1 against the human lung cancer cells (H1299) is similar to oxaliplatin, but higher than transplatin and carboplatin.en_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPharmacology & pharmacyen_US
dc.subjectChemistryen_US
dc.subjectPt(II) complexesen_US
dc.subject2-(Hydroxymethyl)pyridineen_US
dc.subjectPyridine-2-carboxylateen_US
dc.subjectDNA bindingen_US
dc.subjectCytotoxic activityen_US
dc.subjectIn-vitroen_US
dc.subjectMolecular-structureen_US
dc.subjectAntitumor platinumen_US
dc.subject2-acetyl pyridineen_US
dc.subjectPt(II) complexesen_US
dc.subjectMetal-complexesen_US
dc.subjectPalladium(II)en_US
dc.subjectModeen_US
dc.subjectL=2-hydroxypyridineen_US
dc.subject3-hydroxypyridineen_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.meshCrystallography, x-rayen_US
dc.subject.meshDNAen_US
dc.subject.meshDose-response relationship, drugen_US
dc.subject.meshDrug screening assays, antitumoren_US
dc.subject.meshFishesen_US
dc.subject.meshHumansen_US
dc.subject.meshLigandsen_US
dc.subject.meshMaleen_US
dc.subject.meshModels, molecularen_US
dc.subject.meshMolecular structureen_US
dc.subject.meshOrganoplatinum compoundsen_US
dc.subject.meshPicolinic acidsen_US
dc.subject.meshPlasmidsen_US
dc.subject.meshPyridinesen_US
dc.subject.meshRatsen_US
dc.subject.meshSpermatozoaen_US
dc.subject.meshStructure-activity relationshipen_US
dc.titleSynthesis, crystal structures, DNA binding and cytotoxicity of two novel platinum(II) complexes containing 2-(hydroxymethyl)pyridine and pyridine-2-carboxylate ligandsen_US
dc.typeArticleen_US
dc.identifier.wos000316642900041tr_TR
dc.identifier.scopus2-s2.0-84875220138tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı.tr_TR
dc.relation.bapBAPtr_TR
dc.contributor.orcid0000-0002-2849-3332tr_TR
dc.contributor.orcid0000-0002-2717-2430tr_TR
dc.identifier.startpage2117tr_TR
dc.identifier.endpage2122tr_TR
dc.identifier.volume23tr_TR
dc.identifier.issue7tr_TR
dc.relation.journalBioorganic and Medicinal Chemistry Lettersen_US
dc.contributor.buuauthorİçsel, Ceyda-
dc.contributor.buuauthorYılmaz, Veysel Turan-
dc.contributor.buuauthorUlukaya, Engin-
dc.contributor.researcheridK-5792-2018tr_TR
dc.contributor.researcheridL-7238-2018tr_TR
dc.contributor.researcheridAAI-3342-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed23434229tr_TR
dc.subject.wosChemistry, medicinalen_US
dc.subject.wosChemistry, organicen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2 (Chemistry, organic)en_US
dc.wos.quartileQ3 (Chemistry, medicinal)en_US
dc.contributor.scopusid55551960400tr_TR
dc.contributor.scopusid7006269202tr_TR
dc.contributor.scopusid6602927353tr_TR
dc.subject.scopusAntineoplastic Activity; Prodrugs; Transplatinen_US
dc.subject.emtreeAntineoplastic agenten_US
dc.subject.emtreeCarboplatinen_US
dc.subject.emtreeDNAen_US
dc.subject.emtreeOxaliplatinen_US
dc.subject.emtreePlatinum derivativeen_US
dc.subject.emtreeTransplatinen_US
dc.subject.emtreeAnimal cellen_US
dc.subject.emtreeAntineoplastic activityen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBinding affinityen_US
dc.subject.emtreeCancer cellen_US
dc.subject.emtreeCrystal structureen_US
dc.subject.emtreeCytotoxicityen_US
dc.subject.emtreeDNA bindingen_US
dc.subject.emtreeDrug bindingen_US
dc.subject.emtreeDrug determinationen_US
dc.subject.emtreeDrug mechanismen_US
dc.subject.emtreeDrug structureen_US
dc.subject.emtreeDrug synthesisen_US
dc.subject.emtreeFluorescenceen_US
dc.subject.emtreeFluorescence analysisen_US
dc.subject.emtreeGel electrophoresisen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeIn vitro studyen_US
dc.subject.emtreeInfrared radiationen_US
dc.subject.emtreeLung canceren_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreeNuclear magnetic resonanceen_US
dc.subject.emtreeViscosityen_US
dc.subject.emtreeX ray crystallographyen_US
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