Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/30719
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dc.contributor.authorUlukaya, Engin-
dc.date.accessioned2023-01-30T12:48:49Z-
dc.date.available2023-01-30T12:48:49Z-
dc.date.issued2019-12-02-
dc.identifier.citationGençkal, H. M. vd. (2020). "Mixed ligand complexes of Co(II), Ni(II) and Cu(II) with quercetin and diimine ligands: Synthesis, characterization, anti-cancer and anti-oxidant activity". Journal of Biological Inorganic Chemistry, 25(1), 161-177.en_US
dc.identifier.issn0949-8257-
dc.identifier.issn1432-1327-
dc.identifier.urihttps://doi.org/10.1007/s00775-019-01749-z-
dc.identifier.urihttps://link.springer.com/article/10.1007/s00775-019-01749-z-
dc.identifier.urihttp://hdl.handle.net/11452/30719-
dc.description.abstractIn this work, mixed ligand complexes of Co(II) Ni(II) and Cu(II) were synthesized using quercetin and diimine (1,10-phenanthroline or 2,2 '-bipyiridine) ligands. The obtained Ni(II) and Co(II) complexes are new and the Cu(II) complexes are synthesized by different method from the literature. The characterization of complexes was performed by elemental analysis, thermogravimetric analysis, ESI-MS, UV-visible and infrared spectral analyses, magnetic susceptibility and molar conductivity measurements. It was found that quercetin, diimine and metal(II) ion form 1:1:1 complexes. Resulting data supported octahedral geometry for Ni(II) and Co(II) complexes and square pyramidal geometry for Cu(II) complexes. The proposed compositions are [Co(queH-1)Cl(phen)(H2O)]center dot 2H(2)O (1, queH = quercetin, phen = 1,10-phenanthroline), [Ni(queH-1)Cl(phen)(H2O)]center dot 2H(2)O (2), [Cu(queH-1)Cl(phen)]center dot 2.5H(2)O (3) and [Cu(queH-1)Cl(bpy)]center dot 2H(2)O (4, bpy = 2,2 '-bipyiridine). Antioxidant capacity and total phenolic content of complexes measured by Folin-Ciocalteu and ABTS methods. Anti-cancer effect of these compounds were tested against different cancer cells (A549, PC-3, HeLa and MCF-7). Apoptosis identified by the fluorescence imaging, caspase cleaved cytokeratin-18 and flow cytometry analysis (annexin V, caspase 3/7, mitochondria membrane potential and oxidative stress). As a result, Cu(II) complexes are more effective than the other compounds and Complex 3 is a promising anti-cancer compound against breast cancer MCF-7 and MDA-MB-231 cells (IC50 values are 2.4 and 5.4 mu M for 48 h, respectively). Flow cytometry analysis exhibited that Complex 3 caused apoptosis in MCF-7 cells. These results support that Complex 3 has anticancer activity and can be a potential anticancer agent especially in breast cancer.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectFlavonoid complexesen_US
dc.subjectQuercetinen_US
dc.subject1tr_TR
dc.subject10-Phenanthrolineen_US
dc.subject2tr_TR
dc.subject2 '-bipyridineen_US
dc.subjectCytotoxicityen_US
dc.subjectAnti-cancer activityen_US
dc.subjectAntioxidant activityen_US
dc.subjectMitochondria-mediated apoppsisen_US
dc.subjectCell-cycle arresten_US
dc.subjectAntitumor activitiesen_US
dc.subjectCopper(II) complexesen_US
dc.subjectMetal-complexesen_US
dc.subjectII complexesen_US
dc.subjectDNA-bindingen_US
dc.subjectFlavonoidsen_US
dc.subjectActivationen_US
dc.subjectDerivativesen_US
dc.subjectBiochemistry & molecular biologyen_US
dc.subjectChemistryen_US
dc.subject.meshAntineoplastic agentsen_US
dc.subject.meshAntioxidantsen_US
dc.subject.meshCell lineen_US
dc.subject.meshTumoren_US
dc.subject.meshCobalten_US
dc.subject.meshCoordination complexesen_US
dc.subject.meshCopperen_US
dc.subject.meshHumansen_US
dc.subject.meshIminesen_US
dc.subject.meshLigandsen_US
dc.subject.meshNickelen_US
dc.subject.meshQuercetinen_US
dc.subject.meshSpectrum analysisen_US
dc.titleMixed ligand complexes of Co(II), Ni(II) and Cu(II) with quercetin and diimine ligands: Synthesis, characterization, anti-cancer and anti-oxidant activityen_US
dc.typeArticleen_US
dc.identifier.wos000519936700015tr_TR
dc.identifier.scopus2-s2.0-85076348979tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Bölümü.tr_TR
dc.relation.bapOUAP (F)–2014/27tr_TR
dc.contributor.orcid0000-0002-6729-7908tr_TR
dc.contributor.orcid0000-0002-3127-742Xtr_TR
dc.contributor.orcid0000-0002-0026-7755tr_TR
dc.identifier.startpage161tr_TR
dc.identifier.endpage177tr_TR
dc.identifier.volume25tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalJournal of Biological Inorganic Chemistryen_US
dc.contributor.buuauthorGençkal, Hasene-
dc.contributor.buuauthorErkısa, Merve-
dc.contributor.buuauthorPınar, Alper-
dc.contributor.buuauthorŞahin, Saliha-
dc.contributor.buuauthorArı, Ferda-
dc.contributor.researcheridAAH-2892-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed31832781tr_TR
dc.subject.wosBiochemistry & molecular biologyen_US
dc.subject.wosChemistry, inorganic & nuclearen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2 (Chemistry, inorganic & nuclear)en_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid57212275330tr_TR
dc.contributor.scopusid57126208900tr_TR
dc.contributor.scopusid15027401600tr_TR
dc.contributor.scopusid24376085300tr_TR
dc.subject.scopusTaxifolin; Morin; Complexen_US
dc.subject.emtreeAntineoplastic agenten_US
dc.subject.emtreeAntioxidanten_US
dc.subject.emtreeCaspaseen_US
dc.subject.emtreeCaspase 3en_US
dc.subject.emtreeCaspase 7en_US
dc.subject.emtreeCobalt complexen_US
dc.subject.emtreeCopper complexen_US
dc.subject.emtreeCytokeratin 18en_US
dc.subject.emtreeDiimineen_US
dc.subject.emtreeLipocortin 5en_US
dc.subject.emtreePhenol derivativeen_US
dc.subject.emtreeQuercetinen_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeAntineoplastic agenten_US
dc.subject.emtreeAntioxidanten_US
dc.subject.emtreeCobalten_US
dc.subject.emtreeCoordination compounden_US
dc.subject.emtreeCopperen_US
dc.subject.emtreeImineen_US
dc.subject.emtreeLiganden_US
dc.subject.emtreeNickelen_US
dc.subject.emtreeQuercetinen_US
dc.subject.emtreeA-549 cell lineen_US
dc.subject.emtreeABTS radical scavenging assayen_US
dc.subject.emtreeAntineoplastic activityen_US
dc.subject.emtreeAntioxidant activityen_US
dc.subject.emtreeApoptosisen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCell proliferationen_US
dc.subject.emtreeChemical compositionen_US
dc.subject.emtreeComplex formationen_US
dc.subject.emtreeConductanceen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDrug structureen_US
dc.subject.emtreeDrug synthesisen_US
dc.subject.emtreeElectrospray mass spectrometryen_US
dc.subject.emtreeElemental analysisen_US
dc.subject.emtreeFlow cytometryen_US
dc.subject.emtreeFluorescenceen_US
dc.subject.emtreeFolin Ciocalteu methoden_US
dc.subject.emtreeGeometryen_US
dc.subject.emtreeHeLa cell lineen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeIC50en_US
dc.subject.emtreeInfrared spectroscopyen_US
dc.subject.emtreeLigand bindingen_US
dc.subject.emtreeMagnetismen_US
dc.subject.emtreeMCF-7 cell lineen_US
dc.subject.emtreeMDA-MB-231 cell lineen_US
dc.subject.emtreeMitochondrial membrane potentialen_US
dc.subject.emtreeOxidative stressen_US
dc.subject.emtreePC-3 [Human pancreatic carcinoma] cell lineen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeProtein cleavageen_US
dc.subject.emtreeThermal analysisen_US
dc.subject.emtreeThermogravimetryen_US
dc.subject.emtreeUltraviolet C radiationen_US
dc.subject.emtreeChemistryen_US
dc.subject.emtreeProceduresen_US
dc.subject.emtreeSpectroscopyen_US
dc.subject.emtreeTumor cell lineen_US
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