Synthesis of new sulfonamide inhibitors of carbonic anhydrase - [2]
| dc.contributor.author | Arslan, O. | |
| dc.contributor.author | Cakir, U. | |
| dc.contributor.author | Uorap, H.Y. | |
| dc.date.accessioned | 2025-07-03T21:18:13Z | |
| dc.date.issued | 2002 | |
| dc.department | Balıkesir Üniversitesi | |
| dc.description.abstract | Four 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.endpage | 1276 | |
| dc.identifier.issn | 0320-9725 | |
| dc.identifier.issue | 9 | |
| dc.identifier.scopus | 2-s2.0-0036945232 | |
| dc.identifier.scopusquality | N/A | |
| dc.identifier.startpage | 1273 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12462/21253 | |
| dc.identifier.volume | 67 | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | ru | |
| dc.relation.ispartof | Biokhimiya | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_Scopus_20250703 | |
| dc.subject | Carbonic anhydrase | |
| dc.subject | Glaucoma | |
| dc.subject | Inhibition | |
| dc.subject | Sulfonamides | |
| dc.title | Synthesis of new sulfonamide inhibitors of carbonic anhydrase - [2] | |
| dc.type | Article |












