Publication:
Synthesis, crystal structures, in vitro DNA binding, antibacterial and cytotoxic activities of new di- and polynuclear silver(I) saccharinate complexes with tertiary monophosphanes

dc.contributor.authorYılmaz, Sunde Süslüer
dc.contributor.authorBüyükgüngör, Orhan
dc.contributor.buuauthorYılmaz, Veysel Turan
dc.contributor.buuauthorGöçmen, Elif
dc.contributor.buuauthorİçsel, Ceyda
dc.contributor.buuauthorCengiz, Murat
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentVeterinerlik Fakültesi
dc.contributor.departmentKimya Bölümü
dc.contributor.departmentKlinik Öncesi Bilimler Bölümü
dc.contributor.orcid0000-0002-2849-3332
dc.contributor.orcid0000-0002-2717-2430
dc.contributor.researcheridAAI-3342-2021
dc.contributor.researcheridL-7238-2018
dc.contributor.researcheridABE-5935-2020
dc.contributor.scopusid7006269202
dc.contributor.scopusid55992981200
dc.contributor.scopusid55551960400
dc.contributor.scopusid16635026700
dc.date.accessioned2022-09-09T07:11:19Z
dc.date.available2022-09-09T07:11:19Z
dc.date.issued2014-02-05
dc.description.abstractFour new silver(I) saccharinate (sac) complexes, [Ag(mu-sac)(PPh3)](2) (1), [Ag(mu-sac)(PPh2CY)](2) (2), [Ag(mu-sac)(PPhCy2)](2) (3) and [Ag(mu-sac)(PCy3)](n) (4), where PPh3 = triphenylphosphane, PPh2Cy = cyclohexyldiphenylphosphane, PPhCy2 = dicyclohexylphenylphosphane and PCy3 = tricyclohexylphosphane, have been synthesized and fully characterized by elemental analysis, IR, NMR, ESI-MS and single crystal X-ray diffraction. Fluorescence ethidium bromide displacement indicate that all complexes bind to fish sperm (FS) DNA by intercalation with binding constants (K-A) of 29.1 +/- 0.26 x 10(5) M-1 for 1, 2.54 +/- 0.12 x 10(5) M-1 for 2, 2.42 +/- 0.08 x 10(5) M-1 for 3, 0.19 +/- 0.03 x 10(5) M-1 for 4. The relative viscosities of the FS-DNA solutions increase with increasing of the complex concentration, providing strong evidence for the intercalation mode. The gel electrophoresis assay further confirms their binding with the pBR322 plasmid DNA. The MIC values of the silver(I) complexes are generally higher than those of AgNO3 and silver sulfadiazine, but 1 presents a promising activity against Salmonella typhimurium and Staphylococcus aureus. All complexes are highly cytotoxic on human lung carcinoma (A549) and human breast adenocarcinoma (MCF-7) cell lines with IC50 values ranging from 0.82 to 3.13 mu M.
dc.identifier.citationYılmaz, V. T. vd. (2014). "Synthesis, crystal structures, in vitro DNA binding, antibacterial and cytotoxic activities of new di- and polynuclear silver(I) saccharinate complexes with tertiary monophosphanes". Journal of Photochemistry and Photobiology B: Biology, 131, 31-42.
dc.identifier.endpage42
dc.identifier.issn1011-1344
dc.identifier.pubmed24480545
dc.identifier.scopus2-s2.0-84893161859
dc.identifier.startpage31
dc.identifier.urihttps://doi.org/10.1016/j.jphotobiol.2013.12.014
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1011134413002947
dc.identifier.urihttp://hdl.handle.net/11452/28595
dc.identifier.volume131
dc.identifier.wos000333790100004
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherElsevier
dc.relation.bapUAP(F)-2011/36
dc.relation.collaborationYurt içi
dc.relation.journalJournal of Photochemistry and Photobiology B: Biology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectSilver(I)
dc.subjectSaccharinate
dc.subjectPhosphine
dc.subjectDNA binding
dc.subjectAntibacterial activity
dc.subjectCytotoxic activity
dc.subjectX-ray
dc.subjectAntimicrobial activities
dc.subjectHeterocyclic thiones
dc.subjectTriphenylphosphine ligands
dc.subjectAntiproliferative activity
dc.subjectPlatinum(ıı) complexes
dc.subjectMolecular-structures
dc.subjectAnticancer activity
dc.subjectEthidium-bromide
dc.subjectThermal analyses
dc.subjectBiochemistry & molecular biology
dc.subjectBiophysics
dc.subject.emtreeCiprofloxacin
dc.subject.emtreeCisplatin
dc.subject.emtreeGentamicin
dc.subject.emtreeSilver derivative
dc.subject.emtreeSulfadiazine silver
dc.subject.emtreeAntiinfective agent
dc.subject.emtreeAntineoplastic agent
dc.subject.emtreeDNA
dc.subject.emtreePhosphine
dc.subject.emtreePhosphine derivative
dc.subject.emtreeSaccharin
dc.subject.emtreeSilver derivative
dc.subject.emtreeAntibacterial activity
dc.subject.emtreeAntineoplastic activity
dc.subject.emtreeArticle
dc.subject.emtreeBacterial strain
dc.subject.emtreeBinding affinity
dc.subject.emtreeBreast adenocarcinoma
dc.subject.emtreeCarcinoma cell
dc.subject.emtreeControlled study
dc.subject.emtreeCrystal structure
dc.subject.emtreeDNA binding
dc.subject.emtreeDrug cytotoxicity
dc.subject.emtreeDrug synthesis
dc.subject.emtreeElectrospray mass spectrometry
dc.subject.emtreeFluorescence
dc.subject.emtreeFluorescence spectroscopy
dc.subject.emtreeGel electrophoresis
dc.subject.emtreeHuman
dc.subject.emtreeHuman cell
dc.subject.emtreeIn vitro study
dc.subject.emtreeLung carcinoma
dc.subject.emtreeMinimum inhibitory concentration
dc.subject.emtreeNonhuman
dc.subject.emtreeNuclear magnetic resonance
dc.subject.emtreePriority journal
dc.subject.emtreeSalmonella typhimurium
dc.subject.emtreeStaphylococcus aureus
dc.subject.emtreeViscometry
dc.subject.emtreeX ray crystallography
dc.subject.emtreeChemical structure
dc.subject.emtreeChemistry
dc.subject.emtreeDrug effects
dc.subject.emtreeDrug screening
dc.subject.emtreeMetabolism
dc.subject.emtreeMicrobial sensitivity test
dc.subject.emtreeSynthesis
dc.subject.emtreeTumor cell line
dc.subject.meshAnti-bacterial agents
dc.subject.meshAntineoplastic agents
dc.subject.meshCell line, tumor
dc.subject.meshChemistry techniques, synthetic
dc.subject.meshCrystallography, X-ray
dc.subject.meshDNA
dc.subject.meshDrug screening assays, antitumor
dc.subject.meshHumans
dc.subject.meshMicrobial sensitivity tests
dc.subject.meshMolecular structure
dc.subject.meshPhosphines
dc.subject.meshSaccharin
dc.subject.meshSilver compounds
dc.subject.scopusComplex; Diphenyl Ethers; Silver
dc.subject.wosBiochemistry & molecular biology
dc.subject.wosBiophysics
dc.titleSynthesis, crystal structures, in vitro DNA binding, antibacterial and cytotoxic activities of new di- and polynuclear silver(I) saccharinate complexes with tertiary monophosphanes
dc.typeArticle
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Kimya Bölümü
local.contributor.departmentVeterinerlik Fakültesi/Klinik Öncesi Bilimler Bölümü
local.indexed.atScopus
local.indexed.atWOS

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