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dc.contributor.authorArslan, Oktay
dc.date.accessioned2019-09-02T12:03:10Z
dc.date.available2019-09-02T12:03:10Z
dc.date.issued2001en_US
dc.identifier.issn0006-2979
dc.identifier.urihttps://doi.org/ 10.1023/A:1012365424900
dc.identifier.urihttps://hdl.handle.net/20.500.12462/6171
dc.description.abstractInhibitory effects of three new derivatives of 2-acetylamino-1,3,4-thiadiazole-5-sulfonamide on bovine carbonic anhydrase have been investigated. The new compounds are 2-(3-chloropropionylamino)-1,3,4-thiadiazole-5-sulfonamide, 2-(2,2-dichloroacetylamino)-1,3,4-thiadiazole-5-sulfonamide, and 2-(3-phenylpropionylamino)-1,3,4-thiadiazole-5-sulfonamide. The new compounds inhibit the esterase activity of carbonic anhydrase noncompetitively and have inhibition constants and I-50 values very similar to those for 2-acetylamino-1,3,4-thiadiazole-5-sulfonamide, the latter being clinically used in the treatment of glaucoma.en_US
dc.language.isoengen_US
dc.publisherMaik Nauka/Interperiodicaen_US
dc.relation.isversionof10.1023/A:1012365424900en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectInhibitionen_US
dc.subjectBovine Carbonic Anhydraseen_US
dc.subjectSulfonamidesen_US
dc.titleInhibition of bovine carbonic anhydrase by new sulfonamide compoundsen_US
dc.typearticleen_US
dc.relation.journalBiochemistry-Moscowen_US
dc.contributor.departmentFen Edebiyat Fakültesien_US
dc.identifier.volume66en_US
dc.identifier.issue9en_US
dc.identifier.startpage982en_US
dc.identifier.endpage983en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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