Publication:
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

dc.contributor.authorHarrison, William T. A.
dc.contributor.buuauthorİçsel, Ceyda
dc.contributor.buuauthorYılmaz, Veysel T.
dc.contributor.buuauthorArı, Ferda
dc.contributor.buuauthorUlukaya, Engin
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentBiyokimya Ana Bilim Dalı
dc.contributor.departmentBiyoloji Ana Bilim Dalı
dc.contributor.departmentKimya Ana Bilim Dalı
dc.contributor.orcid0000-0002-6729-7908
dc.contributor.orcid0000-0002-2849-3332
dc.contributor.orcid0000-0002-2717-2430
dc.contributor.researcheridAAG-7012-2021
dc.contributor.researcheridL-7238-2018
dc.contributor.researcheridK-5792-2018
dc.contributor.researcheridAAI-3342-2021
dc.contributor.scopusid55551960400
dc.contributor.scopusid7006269202
dc.contributor.scopusid24376085300
dc.contributor.scopusid6602927353
dc.date.accessioned2022-11-11T07:07:25Z
dc.date.available2022-11-11T07:07:25Z
dc.date.issued2013-02
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.
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 .
dc.identifier.endpage394
dc.identifier.issn0223-5234
dc.identifier.issn1768-3254
dc.identifier.pubmed23314052
dc.identifier.scopus2-s2.0-84872160407
dc.identifier.startpage386
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.identifier.volume60
dc.identifier.wos000316242700039
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherElsevier France
dc.relation.collaborationYurt dışı
dc.relation.journalEuropean Journal of Medicinal Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.relation.tubitak111T099
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectPharmacology & pharmacy
dc.subjectTransplatinum complexes
dc.subject2-(Hydroxymethyl)pyridine
dc.subject2-(2-Hydroxyethyl)pyridine
dc.subjectDNA binding
dc.subjectCytotoxic activity
dc.subjectTrans geometry
dc.subjectEthidium-bromide
dc.subjectMetal-complexes
dc.subjectAntitumor
dc.subjectPalladium(II)
dc.subjectPd(II)
dc.subjectLigand
dc.subjectDrugs
dc.subjectRuthenium(II)
dc.subjectFluorescence
dc.subject.emtreeCisplatin
dc.subject.emtreeDNA
dc.subject.emtreePalladium complex
dc.subject.emtreePlasmid DNA
dc.subject.emtreePlatinum complex
dc.subject.emtreePyridine derivative
dc.subject.emtreeTransplatin
dc.subject.emtreeAbsorption spectroscopy
dc.subject.emtreeAnimal cell
dc.subject.emtreeAntineoplastic activity
dc.subject.emtreeArticle
dc.subject.emtreeCancer cell
dc.subject.emtreeCancer cell culture
dc.subject.emtreeCarbon nuclear magnetic resonance
dc.subject.emtreeCell viability
dc.subject.emtreeColon cancer
dc.subject.emtreeConcentration response
dc.subject.emtreeControlled study
dc.subject.emtreeCrystal structure
dc.subject.emtreeCytotoxicity
dc.subject.emtreeDNA binding
dc.subject.emtreeDNA denaturation
dc.subject.emtreeDrug synthesis
dc.subject.emtreeFibroblast
dc.subject.emtreeGel electrophoresis
dc.subject.emtreeHuman
dc.subject.emtreeHuman cell
dc.subject.emtreeIn vitro study
dc.subject.emtreeInfrared spectrophotometry
dc.subject.emtreeInteractions with DNA
dc.subject.emtreeNonhuman
dc.subject.emtreeRat
dc.subject.emtreeStructure analysis
dc.subject.emtreeTitrimetry
dc.subject.emtreeUltraviolet radiation
dc.subject.emtreeViscosity
dc.subject.emtreeX ray diffraction
dc.subject.meshAnimals
dc.subject.meshAntineoplastic agents
dc.subject.meshBinding sites
dc.subject.meshCell line, tumor
dc.subject.meshCell proliferation
dc.subject.meshCHO cells
dc.subject.meshCricetinae
dc.subject.meshDNA
dc.subject.meshDose-response relationship, drug
dc.subject.meshDrug screening assays, antitumor
dc.subject.meshHumans
dc.subject.meshMolecular structure
dc.subject.meshOrganoplatinum compounds
dc.subject.meshPalladium
dc.subject.meshPlatinum
dc.subject.meshPyridines
dc.subject.meshRats
dc.subject.meshStructure-activity relationship
dc.subject.scopusAntineoplastic Activity; Prodrugs; Transplatin
dc.subject.wosChemistry, medicinal
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 studies
dc.typeArticle
dc.wos.quartileQ1
dc.wos.quartileQ1
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Biyoloji Ana Bilim Dalı
local.contributor.departmentFen Edebiyat Fakültesi/Kimya Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Biyokimya Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

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