Publication:
Cu(ii) complex with auxin (3-indoleacetic acid) and an aromatic planar ligand: Synthesis, crystal structure, biomolecular interactions and radical scavenging activity

dc.contributor.authorİnci, Duygu
dc.contributor.authorAydın, Rahmiye
dc.contributor.authorZorlu, Yunus
dc.contributor.buuauthorAYDIN, RAHMİYE
dc.contributor.departmentBursa Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü
dc.contributor.researcheridAAH-8936-2021
dc.date.accessioned2024-06-13T06:14:00Z
dc.date.available2024-06-13T06:14:00Z
dc.date.issued2021-04-30
dc.description.abstractA novel water soluble ternary copper(ii) complex,-[Cu-2(phen)(2)(3-IAA)(2)(H2O)](ClO4)(2)center dot H2O-(phen: 1,10-phenanthroline, 3-IAA: 3-indoleacetic acid), has been synthesized and characterized by elemental CHN analysis, ESI-TOF, FTIR and single-crystal X-ray diffraction techniques. Interaction of the complex with calf thymus DNA (CT-DNA) has been investigated by absorption spectral titration, ethidium bromide (EB) and Hoechst 33258 displacement assay. The interactions between the complex and bovine serum albumin (BSA) were investigated by electronic absorption and fluorescence spectroscopy methods. The experimental results indicate that the fluorescence quenching mechanism between the complex and BSA is a static quenching process. The Stern-Volmer constants, binding constants, binding sites and the corresponding thermodynamic parameters (Delta G, Delta H, Delta S) of BSA + complex systems were determined at different temperatures. The binding distance between the complex and BSA was calculated according to Forster non-radiation energy transfer theory (FRET). The effect of the complex on the conformation of BSA was also examined using synchronous, two dimensional (2D) and three dimensional (3D) fluorescence spectroscopy. Furthermore, the oxygen radical scavenging activity of the complex was determined in terms of IC50, using the DPPH and H2O2 method, to show that it particularly enables electron loss from radical species. This study highlights the importance of indole and moieties in the development of antioxidant agents.
dc.identifier.doi10.1007/s00249-021-01525-5
dc.identifier.eissn1432-1017
dc.identifier.endpage785
dc.identifier.issn0175-7571
dc.identifier.issue5
dc.identifier.startpage771
dc.identifier.urihttps://doi.org/10.1007/s00249-021-01525-5
dc.identifier.urihttps://link.springer.com/article/10.1007/s00249-021-01525-5
dc.identifier.urihttps://hdl.handle.net/11452/42107
dc.identifier.volume50
dc.identifier.wos000645873000001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherSpringer
dc.relation.bapB..Y.G.P-2018/1
dc.relation.journalEuropean Biophysics Journal With Biophysics Letters
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectSerum-albumin
dc.subjectCu(ii)
dc.subject1,10-phenanthroline
dc.subjectAuxin (3-indoleacetic acid)
dc.subjectBiomolecular interactions
dc.subjectRadical scavenging activity
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectBiophysics
dc.titleCu(ii) complex with auxin (3-indoleacetic acid) and an aromatic planar ligand: Synthesis, crystal structure, biomolecular interactions and radical scavenging activity
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublication664dd2c7-f9b5-4cfd-ad90-163ae2c8685f
relation.isAuthorOfPublication.latestForDiscovery664dd2c7-f9b5-4cfd-ad90-163ae2c8685f

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