Synthesis of new sulfonamide inhibitors of carbonic anhydrase - [2]

dc.contributor.authorArslan, O.
dc.contributor.authorCakir, U.
dc.contributor.authorUorap, H.Y.
dc.date.accessioned2025-07-03T21:18:13Z
dc.date.issued2002
dc.departmentBalıkesir Üniversitesi
dc.description.abstractFour different derivatives of aromatic sulfonamides have been synthesized: 1,2-bis[(4-sulfonamidobenzamide)ethoxy]ethane (SBAM), 1,2-bis[(4-sulfonamidobenzoate)ethoxy]ethane, 1,2-bis[(2,4-dichloro-5-sulfonamidobenzamide)ethoxy]ethane, and 1,2-bis[(2,4-dichloro-5-sulfonamidobenzoate)ethoxy]ethane. SBAM is a most potent inhibitor on ciliary epithelium carbonic anhydrase and is approximately 13 times more active against carbonic anhydrase isoform II than against isoform I.
dc.identifier.endpage1276
dc.identifier.issn0320-9725
dc.identifier.issue9
dc.identifier.scopus2-s2.0-0036945232
dc.identifier.scopusqualityN/A
dc.identifier.startpage1273
dc.identifier.urihttps://hdl.handle.net/20.500.12462/21253
dc.identifier.volume67
dc.indekslendigikaynakScopus
dc.language.isoru
dc.relation.ispartofBiokhimiya
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20250703
dc.subjectCarbonic anhydrase
dc.subjectGlaucoma
dc.subjectInhibition
dc.subjectSulfonamides
dc.titleSynthesis of new sulfonamide inhibitors of carbonic anhydrase - [2]
dc.typeArticle

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