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dc.contributor.authorKarataş, Mert Olgun
dc.contributor.authorAlıcı, Bülent
dc.contributor.authorÇakır, Ümit
dc.contributor.authorÇetinkaya, Engin
dc.contributor.authorDemir, Dudu
dc.contributor.authorErgün, Adem
dc.contributor.authorGençer, Nahit
dc.contributor.authorArslan, Oktay
dc.date.accessioned2019-10-17T10:31:54Z
dc.date.available2019-10-17T10:31:54Z
dc.date.issued2014en_US
dc.identifier.issn2169-1401
dc.identifier.issn2169-141X
dc.identifier.urihttps://doi.org/10.3109/21691401.2013.794352
dc.identifier.urihttps://hdl.handle.net/20.500.12462/8125
dc.descriptionGençer, Nahit (Balıkesir Author)en_US
dc.description.abstractIn the current study, a series of 4-chloromethyl-7-hydroxy-coumarin derivatives containing imidazolium, benzimidazolium, bisbenzimidazolium and quaternary ammonium salts were synthesized, characterized and the inhibition effects of the derivatives on human carbonic anhydrases (hCA I and hCA II) were investigated as in vitro. Structures of these coumarins were confirmed by FT-IR, (1)H NMR, (13)C NMR and LC-MS analyses. Structure activity relationship study showed that 3d (IC50: 79 mu m M for hCA I and 88 m M for hCA II) performed higher inhibitory activity than others.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.isversionof10.3109/21691401.2013.794352en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectBenzimidazoliumen_US
dc.subjectCarbonic Anhydraseen_US
dc.subjectCoumarinen_US
dc.subjectImidazoliumen_US
dc.subjectInhibitionen_US
dc.titleNew coumarin derivatives as carbonic anhydrase inhibitorsen_US
dc.typearticleen_US
dc.relation.journalArtificial Cells Nanomedicine and Biotechnologyen_US
dc.contributor.departmentFen Edebiyat Fakültesien_US
dc.identifier.volume42en_US
dc.identifier.issue3en_US
dc.identifier.startpage192en_US
dc.identifier.endpage198en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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