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http://hdl.handle.net/11452/29450
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Harrison, William T. A. | - |
dc.date.accessioned | 2022-11-11T07:07:25Z | - |
dc.date.available | 2022-11-11T07:07:25Z | - |
dc.date.issued | 2013-02 | - |
dc.identifier.citation | İçsel, 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.issn | 0223-5234 | - |
dc.identifier.issn | 1768-3254 | - |
dc.identifier.uri | https://doi.org/10.1016/j.ejmech.2012.12.002 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0223523412007246 | - |
dc.identifier.uri | http://hdl.handle.net/11452/29450 | - |
dc.description.abstract | Four 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.iso | en | en_US |
dc.publisher | Elsevier France | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Pharmacology & pharmacy | en_US |
dc.subject | Transplatinum complexes | en_US |
dc.subject | 2-(Hydroxymethyl)pyridine | en_US |
dc.subject | 2-(2-Hydroxyethyl)pyridine | en_US |
dc.subject | DNA binding | en_US |
dc.subject | Cytotoxic activity | en_US |
dc.subject | Trans geometry | en_US |
dc.subject | Ethidium-bromide | en_US |
dc.subject | Metal-complexes | en_US |
dc.subject | Antitumor | en_US |
dc.subject | Palladium(II) | en_US |
dc.subject | Pd(II) | en_US |
dc.subject | Ligand | en_US |
dc.subject | Drugs | en_US |
dc.subject | Ruthenium(II) | en_US |
dc.subject | Fluorescence | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Antineoplastic agents | en_US |
dc.subject.mesh | Binding sites | en_US |
dc.subject.mesh | Cell line, tumor | en_US |
dc.subject.mesh | Cell proliferation | en_US |
dc.subject.mesh | CHO cells | en_US |
dc.subject.mesh | Cricetinae | en_US |
dc.subject.mesh | DNA | en_US |
dc.subject.mesh | Dose-response relationship, drug | en_US |
dc.subject.mesh | Drug screening assays, antitumor | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Molecular structure | en_US |
dc.subject.mesh | Organoplatinum compounds | en_US |
dc.subject.mesh | Palladium | en_US |
dc.subject.mesh | Platinum | en_US |
dc.subject.mesh | Pyridines | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Structure-activity relationship | en_US |
dc.title | 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 | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000316242700039 | tr_TR |
dc.identifier.scopus | 2-s2.0-84872160407 | tr_TR |
dc.relation.tubitak | 111T099 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0002-6729-7908 | tr_TR |
dc.contributor.orcid | 0000-0002-2849-3332 | tr_TR |
dc.contributor.orcid | 0000-0002-2717-2430 | tr_TR |
dc.identifier.startpage | 386 | tr_TR |
dc.identifier.endpage | 394 | tr_TR |
dc.identifier.volume | 60 | tr_TR |
dc.relation.journal | European Journal of Medicinal Chemistry | en_US |
dc.contributor.buuauthor | İçsel, Ceyda | - |
dc.contributor.buuauthor | Yılmaz, Veysel T. | - |
dc.contributor.buuauthor | Arı, Ferda | - |
dc.contributor.buuauthor | Ulukaya, Engin | - |
dc.contributor.researcherid | AAG-7012-2021 | tr_TR |
dc.contributor.researcherid | L-7238-2018 | tr_TR |
dc.contributor.researcherid | K-5792-2018 | tr_TR |
dc.contributor.researcherid | AAI-3342-2021 | tr_TR |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.identifier.pubmed | 23314052 | tr_TR |
dc.subject.wos | Chemistry, medicinal | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q1 | en_US |
dc.contributor.scopusid | 55551960400 | tr_TR |
dc.contributor.scopusid | 7006269202 | tr_TR |
dc.contributor.scopusid | 24376085300 | tr_TR |
dc.contributor.scopusid | 6602927353 | tr_TR |
dc.subject.scopus | Antineoplastic Activity; Prodrugs; Transplatin | en_US |
dc.subject.emtree | Cisplatin | en_US |
dc.subject.emtree | DNA | en_US |
dc.subject.emtree | Palladium complex | en_US |
dc.subject.emtree | Plasmid DNA | en_US |
dc.subject.emtree | Platinum complex | en_US |
dc.subject.emtree | Pyridine derivative | en_US |
dc.subject.emtree | Transplatin | en_US |
dc.subject.emtree | Absorption spectroscopy | en_US |
dc.subject.emtree | Animal cell | en_US |
dc.subject.emtree | Antineoplastic activity | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Cancer cell | en_US |
dc.subject.emtree | Cancer cell culture | en_US |
dc.subject.emtree | Carbon nuclear magnetic resonance | en_US |
dc.subject.emtree | Cell viability | en_US |
dc.subject.emtree | Colon cancer | en_US |
dc.subject.emtree | Concentration response | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Crystal structure | en_US |
dc.subject.emtree | Cytotoxicity | en_US |
dc.subject.emtree | DNA binding | en_US |
dc.subject.emtree | DNA denaturation | en_US |
dc.subject.emtree | Drug synthesis | en_US |
dc.subject.emtree | Fibroblast | en_US |
dc.subject.emtree | Gel electrophoresis | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Human cell | en_US |
dc.subject.emtree | In vitro study | en_US |
dc.subject.emtree | Infrared spectrophotometry | en_US |
dc.subject.emtree | Interactions with DNA | en_US |
dc.subject.emtree | Nonhuman | en_US |
dc.subject.emtree | Rat | en_US |
dc.subject.emtree | Structure analysis | en_US |
dc.subject.emtree | Titrimetry | en_US |
dc.subject.emtree | Ultraviolet radiation | en_US |
dc.subject.emtree | Viscosity | en_US |
dc.subject.emtree | X ray diffraction | en_US |
Appears in Collections: | PubMed Scopus Web of Science |
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