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dc.contributor.authorOzdemir, Ummuhan O.
dc.contributor.authorOzbek, Neslihan
dc.contributor.authorGenc, Zuhal Karagoz
dc.contributor.authorIlbiz, Firdevs
dc.contributor.authorGunduzalp, Ayla Balaban
dc.date.accessioned2019-11-24T20:38:21Z
dc.date.available2019-11-24T20:38:21Z
dc.date.issued2017
dc.identifier.issn0022-2860
dc.identifier.issn1872-8014
dc.identifier.urihttps://dx.doi.org/10.1016/j.molstruc.2017.02.101
dc.identifier.urihttps://hdl.handle.net/20.500.12513/2510
dc.descriptionWOS: 000399517500009en_US
dc.description.abstractSilver(I) complexes of alkyl sulfonic acide hydrazides were newly synthesized as homologous series. Methanesulfonic acide hydrazide (L1), ethanesulfonic acide hydrazide (L2), propanesulfonic acide hydrazide (L3) and butanesulfonic acide hydrazide (L4) were used for complexation with Ag(I) ions. The silver complexes obtained in the mol ratio of 1:2 have the structural formula as Ag(L1)(2)NO3 (I), Ag(L2)(2)NO3 (II). Ag(L3)(2)NO3 (III), (Ag(L4)(2)NO3 (IV). The Ag(I) complexes exhibit distorted linear two -fold coordination in [AgL2](+) cations with uncoordinated nitrates. Ligands are chelated with silver(I) ions through unsubstituted primary nitrogen in hydrazide group. Ag(I) complexes were characterized by using elemental analysis, spectroscopic methods (FT-IR, LC-MS), magnetic susceptibility and conductivity measurements. Silver(1) complexes were optimized using PBEPBE/LanL2DZ/DEF2SV basic set performed by DFT method with the Gaussian 09 program package. The geometrical parameters, frontier molecular orbitals (HOMOs and LUMOs) and molecular electrostatic potential (MEP) mapped surfaces of the optimized geometries were also determined by this quantum set. The anticancer activities of silver(I) complexes on MCF-7 human breast cancer cell line were investigated by comparing IC50 values. The antibacterial activities of complexes were studied against Gram positive bacteria: S. aureus ATCC 6538, B. subtilis ATCC 6633, B. cereus NRRL-B-3711, E. faecalis ATCC 29212 and Gram negative bacteria: E. coli ATCC 11230, P. aeruginosa ATCC 15442, K. pneumonia ATCC 70063 by using disc diffusion method. The inhibition activities of Ag(I) complexes on carbonic anhydrase II enzyme (hCA II) were also investigated by comparing IC50 and Ki values. The biological activity screening shows that Ag(I) complex of butanesulfonicacidehydrazide (IV) has the highest activity against tested breast cancer cell lines MCF-7, Gram positive/Gram negative bacteria and carbonic anhydrase II (hCA II) isoenzyme. (C)2017 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipGazi University Research FoundGazi University [05/2012-12]en_US
dc.description.sponsorshipThis research was supported by Gazi University Research Found under Project No 05/2012-12. We thank Ankara University, Faculty of Pharmacy. Central Labs. for allocation of time at the Mass Spectra and Elemental Analyses.en_US
dc.language.isoengen_US
dc.publisherELSEVIER SCIENCE BVen_US
dc.relation.isversionof10.1016/j.molstruc.2017.02.101en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSilver(I) complexesen_US
dc.subjectAlkyl sulfonic acide hydrazideen_US
dc.subjectAnticanceren_US
dc.subjectAntibacterialen_US
dc.subjectAnti carbonic anhydrase IIen_US
dc.titleNew bioactive silver(I) complexes: Synthesis, characterization, anticancer, antibacterial and anticarbonic anhydrase II activitiesen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF MOLECULAR STRUCTUREen_US
dc.contributor.departmentKırşehir Ahi Evran Üniversitesi, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.identifier.volume1138en_US
dc.identifier.startpage55en_US
dc.identifier.endpage63en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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