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dc.contributor.authorRifati-Nixha, Arleta
dc.contributor.authorArslan, Mustafa
dc.contributor.authorGencer, Nahit
dc.contributor.authorÇıkrıkcı, Kübra
dc.contributor.authorGökçe, Başak
dc.date.accessioned2021-02-03T08:43:05Z
dc.date.available2021-02-03T08:43:05Z
dc.date.issued2019en_US
dc.identifier.issn1095-6670
dc.identifier.issn1099-0461
dc.identifier.urihttps://doi.org/10.1002/jbt.22306
dc.identifier.urihttps://hdl.handle.net/20.500.12462/11040
dc.descriptionGencer, Nahit (Balikesir Author)en_US
dc.description.abstractThe synthesis of carbazole containing pyridopyrimidine-substituted sulfonamide derivatives (3a-i) and their inhibitory effects on human carbonic anhydrase (hCA) I and II were studied. Spectral data and elemental analysis confirmed the structures of the compounds synthesized. The results show that all the synthesized compounds inhibited the CA I and II activities. Among them, 3a was found to be the most active (K-i: 14 mu M) for hCA I and 3f (K-i: 126 mu M) for hCA II.en_US
dc.description.sponsorshipSakarya Universitesi 2016-02-04-018 Balikesir University 2017/166en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1002/jbt.22306en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectCarbazoleen_US
dc.subjectCarbonic Anhydraseen_US
dc.subjectPyridopyrimidineen_US
dc.subjectSulfonamideen_US
dc.titleSynthesis of carbazole bearing pyridopyrimidine-substituted sulfonamide derivatives and studies their carbonic anhydrase enzyme activityen_US
dc.typearticleen_US
dc.relation.journalJournal of Biochemical and Molecular Toxicologyen_US
dc.contributor.departmentFen Edebiyat Fakültesien_US
dc.contributor.authorID0000-0001-7092-8857en_US
dc.identifier.volume33en_US
dc.identifier.issue6en_US
dc.identifier.startpage1en_US
dc.identifier.endpage6en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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