Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/30761
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dc.contributor.authorUlukaya, Engin-
dc.date.accessioned2023-01-31T13:40:44Z-
dc.date.available2023-01-31T13:40:44Z-
dc.date.issued2019-07-02-
dc.identifier.citationAlper, P. vd. (2019). ''Synthesis, characterization, anticancer and antioxidant activity of new nickel(II) and copper(II) flavonoid complexes''. Journal of Molecular Structure, 1196, 783-792.en_US
dc.identifier.issn0022-2860-
dc.identifier.issn1872-8014-
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2019.07.009-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0022286019308439-
dc.identifier.urihttp://hdl.handle.net/11452/30761-
dc.description.abstractFlavonoids are natural products which are known to have biological activity for human health. In this study, new mixed ligand complexes of Ni(II) and Cu(II) were synthesized by using flavonoid (quercetin or naringenin) and heterocyclic imine (2,2':6',2 ''-terpyridine or 2,2'-bipyiridine) ligands. The new complexes are [Ni(narH-1)(terpy)Cl]center dot 4H(2)O (1, nar = naringenin, terpy = 2,2':6',2 ''-terpyridine), [Cu(narH-1)(terpy)Cl]center dot H2O (2), and [Cu(queH-1)(bpy)(O3N)]center dot 1.5H(2)O (3, que = quercetin, bpy = 2,2'-bipyiridine). The structural features of the synthesized mixed ligand complexes were investigated using elemental analysis, thermogravimetric analysis, Fourier transform infrared spectroscopy, magnetic susceptibility and molar conductivity measurements. The resulting data demonstrated an octahedral geometry for Complex 1 and Complex 2 and square pyramidal geometry for Complex 3. Antioxidant capacity and total phenolic content of Complexes 1-3 were measured by the Folin-Ciocalteu and ABTS methods. Anti- proliferative effect of complexes were tested by SRB and ATP assays on MCF-7 (breast cancer), A549 (nonsmall cell lung cancer), PC-3 (prostate cancer) and HeLa (human cervical cancer) cell lines. Apoptosis was identified using by the fluorescence imaging, caspase cleaved cytokeratin-18 and flow cytometry analysis. Complex 2 and 3 had high total phenolic content and antioxidant activity. Complex 2 was found to show selective cytotoxicity through the induction of apoptosis on MCF-7 cells with having a very low IC50 value (<0.8 mu M; the half maximum inhibitory concentration) while its ligands showed much higher cytotoxicity (IC50 > 50 mu M). In conclusion, Complex 2 is a highly promising and novel compound for breast cancer and warrants further animal experiments. (C) 2019 Elsevier B.V. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChemistryen_US
dc.subjectNi(II) and Cu(II) flavonoid complexesen_US
dc.subjectCytotoxicityen_US
dc.subjectAntioxidant activityen_US
dc.subjectCancer cellsen_US
dc.subjectCell-cycle arresten_US
dc.subjectAntitumor activitiesen_US
dc.subjectInduced Apoptosisen_US
dc.subjectMetal-complexesen_US
dc.subjectDna-bindingen_US
dc.subjectNaringeninen_US
dc.subjectGrowthen_US
dc.subject2,2'-bipyridineen_US
dc.subjectActivationen_US
dc.subjectZinc(II)en_US
dc.subjectAntioxidantsen_US
dc.subjectBioactivityen_US
dc.subjectCell cultureen_US
dc.subjectCell deathen_US
dc.subjectComplexationen_US
dc.subjectCopper compoundsen_US
dc.subjectCopper compoundsen_US
dc.subjectDiseasesen_US
dc.subjectFlavonoidsen_US
dc.subjectFluorescence imagingen_US
dc.subjectFourier transform infrared spectroscopyen_US
dc.subjectLanthanum compoundsen_US
dc.subjectLigandsen_US
dc.subjectMagnetic susceptibilityen_US
dc.subjectPhenolsen_US
dc.subjectSynthesis (chemical)en_US
dc.subjectThermogravimetric analysisen_US
dc.subjectAnti-oxidant activitiesen_US
dc.subjectAntiproliferative effecten_US
dc.subjectCancer cellsen_US
dc.subjectFlavonoiden_US
dc.subjectFlow cytometry analysisen_US
dc.subjectInhibitory concentrationen_US
dc.subjectNon small cell lung canceren_US
dc.subjectSquare-pyramidal geometryen_US
dc.subjectNickel compoundsen_US
dc.titleSynthesis, characterization, anticancer and antioxidant activity of new nickel(II) and copper(II) flavonoid complexesen_US
dc.typeArticleen_US
dc.identifier.wos000487930600079tr_TR
dc.identifier.scopus2-s2.0-85068520445tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.relation.bapOUAP (F)-2014/27tr_TR
dc.contributor.orcid0000-0002-0026-7755tr_TR
dc.contributor.orcid0000-0002-6729-7908tr_TR
dc.contributor.orcid0000-0002-3127-742Xtr_TR
dc.identifier.startpage783tr_TR
dc.identifier.endpage792tr_TR
dc.identifier.volume1196tr_TR
dc.relation.journalJournal of Molecular Structureen_US
dc.contributor.buuauthorAlper, Pınar-
dc.contributor.buuauthorErkisa, Merve-
dc.contributor.buuauthorGenckal, Hasene Mutlu-
dc.contributor.buuauthorSahin, Saliha-
dc.contributor.buuauthorAri, Ferda-
dc.contributor.researcheridAAH-2888-2021tr_TR
dc.contributor.researcheridAAG-7012-2021tr_TR
dc.contributor.researcheridAAM-1001-2020tr_TR
dc.contributor.researcheridAAH-2892-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.subject.wosChemistry, physicalen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid24376085300tr_TR
dc.contributor.scopusid15027401600tr_TR
dc.contributor.scopusid57212275330tr_TR
dc.contributor.scopusid57126208900tr_TR
dc.contributor.scopusid57197858774tr_TR
dc.subject.scopusTaxifolin; Morin; Complexen_US
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