Cu (II) tyrosinate complexes containing methyl substituted phenanthrolines: synthesis, x-ray crystal structures, biomolecular interactions, antioxidant activity, ros generation and cytotoxicity

dc.contributor.authorCosut, Bunyemin
dc.contributor.authorZorlu, Yunus
dc.contributor.buuauthorInci, Duygu
dc.contributor.buuauthorAydın, Rahmiye
dc.contributor.buuauthorVatan, Ozgür
dc.contributor.buuauthorHüriyet, Huzeyfe
dc.contributor.buuauthorCinkılıç, Nilufer
dc.contributor.departmentBursa Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya, Anorganik Kimya Bölümü.tr_TR
dc.contributor.orcid0000-0002-0483-9642tr_TR
dc.contributor.orcid0000-0002-3595-6286tr_TR
dc.contributor.researcheridAAH-8936-2021tr_TR
dc.contributor.researcheridAAH-5296-2021tr_TR
dc.contributor.researcheridG-2201-2019tr_TR
dc.contributor.scopusid55082306300tr_TR
dc.contributor.scopusid56261495600tr_TR
dc.contributor.scopusid16235098100tr_TR
dc.contributor.scopusid57201093675tr_TR
dc.contributor.scopusid26533892300tr_TR
dc.date.accessioned2024-02-13T11:30:00Z
dc.date.available2024-02-13T11:30:00Z
dc.date.issued2019-01
dc.description.abstractIn this paper, three new copper (II) complexes, [Cu(4-mphen)(tyr)(H2O)]ClO4 (1), [Cu(5-mphen)(tyr)(H2O)]ClO4 center dot 1.5H(2)O (2) and [Cu (tmphen)(tyr)(NO3)]0.5H(2)O (3) (4-mphen: 4-methyl-1,10-phenanthroline, 5-mphen: 5-methyl-1,10-phenanthroline, tmphen: 3,4,7,8-tetramethyl-1,10-phenanthroline and tyr: L-tyrosine), were synthesized and characterized using elemental analyses, FT-IR, ESI-MS, cyclic voltammetry and single-crystal X-ray diffraction. It was found that the complexes adopt a distorted five-coordinate square pyramidal geometry. The interaction of the three complexes with calf thymus DNA was also investigated using UV-visible absorption spectra, ethidium bromide and Hoechst 33258 displacement assay and thermal denaturation. The DNA cleavage activity of the complexes, monitored using gel electrophoresis, showed significant damage of the pUC19 plasmid DNA. Binding activity of bovine serum albumin (BSA) reveals that these complexes can strongly quench the fluorescence of BSA through a static quenching mechanism. The results suggested that interaction of the complexes with DNA occurred through a partial intercalation into the minor grooves of DNA. In addition, interaction of the complexes with bovine serum albumin quenched the fluorescence emission of the tryptophan residues of the protein binding constants and thermodynamic parameters were obtained from the fluorescence quenching experiments at different temperatures. Free radical scavenging activities of the complexes were determined by various in vitro assays such as 1,1-diphenyl-2-picryl-hydrazyl free radicals (DPPH) and H2O2 scavenging methods. In addition, the cytotoxicity of these complexes in vitro on tumor cell lines (Caco-2 and MCF-7) was examined by XTT and showed better antitumor effect on the tested cells. ROS (reactive oxygen species) and comet experiments are consistent with each other and these complexes lead to DNA damage via the production of ROS. The effect of the hydrophobic properties of the synthesized complexes on DNA and BSA binding activities were discussed.en_US
dc.description.sponsorship
dc.identifier.citationInci, D. vd. (2019). ''Cu (II) tyrosinate complexes containing methyl substituted phenanthrolines: synthesis, x-ray crystal structures, biomolecular interactions, antioxidant activity, ros generation and cytotoxicity''. Applied Organometallic Chemistry, 33(1).en_US
dc.identifier.issn0268-2605
dc.identifier.issn1099-0739
dc.identifier.issue1tr_TR
dc.identifier.pubmed
dc.identifier.scopus2-s2.0-85056134449tr_TR
dc.identifier.urihttps://doi.org/10.1002/aoc.4652en_US
dc.identifier.urihttps://hdl.handle.net/11452/39675en_US
dc.identifier.volume33tr_TR
dc.identifier.wos000454321800022tr_TR
dc.indexed.pubmed
dc.indexed.scopusScopusen_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.bap(OUAP (F)-2015/14)en_US
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationSanayitr_TR
dc.relation.journalApplied Organometallic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.relation.tubitak2211-Ctr_TR
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectChemistryen_US
dc.subjectCu (II) complexesen_US
dc.subjectL-tyrosineen_US
dc.subjectMethyl substituted phenanthrolinesen_US
dc.subjectDna/bsa interactionsen_US
dc.subjectRos generation and cytotoxicityen_US
dc.subjectBovine serum-albuminen_US
dc.subjectEfficient chemical nucleaseen_US
dc.subjectMixed-ligand complexesen_US
dc.subjectIn-vitro cytotoxicityen_US
dc.subjectCopper(II) complexesen_US
dc.subjectMetal-complexesen_US
dc.subjectDna cleavageen_US
dc.subjectProtease activitiesen_US
dc.subjectAromatic ringen_US
dc.subjectAmino-acidsen_US
dc.subjectAssaysen_US
dc.subjectBiochemistryen_US
dc.subjectBody fluidsen_US
dc.subjectCell cultureen_US
dc.subjectComplexationen_US
dc.subjectCyclic voltammetryen_US
dc.subjectCytotoxicityen_US
dc.subjectDnaen_US
dc.subjectElectrophoresisen_US
dc.subjectFluorescence quenchingen_US
dc.subjectFree radicalsen_US
dc.subjectMammalsen_US
dc.subjectSingle crystalsen_US
dc.subjectSurface plasmon resonanceen_US
dc.subjectSynthesis (chemical)en_US
dc.subjectBiomolecular interactionsen_US
dc.subjectCu complexesen_US
dc.subjectFree radical scavenging activityen_US
dc.subjectl-Tyrosineen_US
dc.subjectPhenanthrolinesen_US
dc.subjectRos generationsen_US
dc.subjectSingle crystal x-ray diffractionen_US
dc.subjectVisible absorption spectraen_US
dc.subjectCopper compoundsen_US
dc.subject.scopusComplex; Viscometry; Schiff Basesen_US
dc.subject.wosChemistry, applieden_US
dc.subject.wosChemistry, inorganic & nuclearen_US
dc.titleCu (II) tyrosinate complexes containing methyl substituted phenanthrolines: synthesis, x-ray crystal structures, biomolecular interactions, antioxidant activity, ros generation and cytotoxicityen_US
dc.typeArticleen_US
dc.wos.quartileQ1en_US

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