Publication:
Mixed ligand complexes of Co(II), Ni(II) and Cu(II) with quercetin and diimine ligands: Synthesis, characterization, anti-cancer and anti-oxidant activity

dc.contributor.authorUlukaya, Engin
dc.contributor.buuauthorGençkal, Hasene
dc.contributor.buuauthorErkısa, Merve
dc.contributor.buuauthorPınar, Alper
dc.contributor.buuauthorŞahin, Saliha
dc.contributor.buuauthorArı, Ferda
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentBiyoloji Bölümü
dc.contributor.departmentKimya Bölümü
dc.contributor.orcid0000-0002-6729-7908
dc.contributor.orcid0000-0002-3127-742X
dc.contributor.orcid0000-0002-0026-7755
dc.contributor.researcheridAAH-2892-2021
dc.contributor.scopusid57212275330
dc.contributor.scopusid57126208900
dc.contributor.scopusid15027401600
dc.contributor.scopusid24376085300
dc.date.accessioned2023-01-30T12:48:49Z
dc.date.available2023-01-30T12:48:49Z
dc.date.issued2019-12-02
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.
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.
dc.identifier.endpage177
dc.identifier.issn0949-8257
dc.identifier.issn1432-1327
dc.identifier.issue1
dc.identifier.pubmed31832781
dc.identifier.scopus2-s2.0-85076348979
dc.identifier.startpage161
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.identifier.volume25
dc.identifier.wos000519936700015
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherSpringer
dc.relation.bapOUAP (F)–2014/27
dc.relation.collaborationYurt içi
dc.relation.journalJournal of Biological Inorganic Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectFlavonoid complexes
dc.subjectQuercetin
dc.subject1
dc.subject10-Phenanthroline
dc.subject2
dc.subject2 '-bipyridine
dc.subjectCytotoxicity
dc.subjectAnti-cancer activity
dc.subjectAntioxidant activity
dc.subjectMitochondria-mediated apoppsis
dc.subjectCell-cycle arrest
dc.subjectAntitumor activities
dc.subjectCopper(II) complexes
dc.subjectMetal-complexes
dc.subjectII complexes
dc.subjectDNA-binding
dc.subjectFlavonoids
dc.subjectActivation
dc.subjectDerivatives
dc.subjectBiochemistry & molecular biology
dc.subjectChemistry
dc.subject.emtreeAntineoplastic agent
dc.subject.emtreeAntioxidant
dc.subject.emtreeCaspase
dc.subject.emtreeCaspase 3
dc.subject.emtreeCaspase 7
dc.subject.emtreeCobalt complex
dc.subject.emtreeCopper complex
dc.subject.emtreeCytokeratin 18
dc.subject.emtreeDiimine
dc.subject.emtreeLipocortin 5
dc.subject.emtreePhenol derivative
dc.subject.emtreeQuercetin
dc.subject.emtreeUnclassified drug
dc.subject.emtreeAntineoplastic agent
dc.subject.emtreeAntioxidant
dc.subject.emtreeCobalt
dc.subject.emtreeCoordination compound
dc.subject.emtreeCopper
dc.subject.emtreeImine
dc.subject.emtreeLigand
dc.subject.emtreeNickel
dc.subject.emtreeQuercetin
dc.subject.emtreeA-549 cell line
dc.subject.emtreeABTS radical scavenging assay
dc.subject.emtreeAntineoplastic activity
dc.subject.emtreeAntioxidant activity
dc.subject.emtreeApoptosis
dc.subject.emtreeArticle
dc.subject.emtreeCell proliferation
dc.subject.emtreeChemical composition
dc.subject.emtreeComplex formation
dc.subject.emtreeConductance
dc.subject.emtreeControlled study
dc.subject.emtreeDrug structure
dc.subject.emtreeDrug synthesis
dc.subject.emtreeElectrospray mass spectrometry
dc.subject.emtreeElemental analysis
dc.subject.emtreeFlow cytometry
dc.subject.emtreeFluorescence
dc.subject.emtreeFolin Ciocalteu method
dc.subject.emtreeGeometry
dc.subject.emtreeHeLa cell line
dc.subject.emtreeHuman
dc.subject.emtreeHuman cell
dc.subject.emtreeIC50
dc.subject.emtreeInfrared spectroscopy
dc.subject.emtreeLigand binding
dc.subject.emtreeMagnetism
dc.subject.emtreeMCF-7 cell line
dc.subject.emtreeMDA-MB-231 cell line
dc.subject.emtreeMitochondrial membrane potential
dc.subject.emtreeOxidative stress
dc.subject.emtreePC-3 [Human pancreatic carcinoma] cell line
dc.subject.emtreePriority journal
dc.subject.emtreeProtein cleavage
dc.subject.emtreeThermal analysis
dc.subject.emtreeThermogravimetry
dc.subject.emtreeUltraviolet C radiation
dc.subject.emtreeChemistry
dc.subject.emtreeProcedures
dc.subject.emtreeSpectroscopy
dc.subject.emtreeTumor cell line
dc.subject.meshAntineoplastic agents
dc.subject.meshAntioxidants
dc.subject.meshCell line
dc.subject.meshTumor
dc.subject.meshCobalt
dc.subject.meshCoordination complexes
dc.subject.meshCopper
dc.subject.meshHumans
dc.subject.meshImines
dc.subject.meshLigands
dc.subject.meshNickel
dc.subject.meshQuercetin
dc.subject.meshSpectrum analysis
dc.subject.scopusTaxifolin; Morin; Complex
dc.subject.wosBiochemistry & molecular biology
dc.subject.wosChemistry, inorganic & nuclear
dc.titleMixed ligand complexes of Co(II), Ni(II) and Cu(II) with quercetin and diimine ligands: Synthesis, characterization, anti-cancer and anti-oxidant activity
dc.typeArticle
dc.wos.quartileQ2 (Chemistry, inorganic & nuclear)
dc.wos.quartileQ3
dc.wos.quartileQ2
dc.wos.quartileQ3
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Kimya Bölümü
local.contributor.departmentFen Edebiyat Fakültesi/Biyoloji Bölümü
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

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