| dc.contributor.author | Arslan, Oktay | |
| dc.contributor.author | Çakır, Ümit | |
| dc.contributor.author | Uğraş, Halil İbrahim | |
| dc.date.accessioned | 2019-08-28T10:32:37Z | |
| dc.date.available | 2019-08-28T10:32:37Z | |
| dc.date.issued | 2002 | en_US |
| dc.identifier.issn | 0006-2979 | |
| dc.identifier.uri | https://doi.org/10.1023/A:1020538422592 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12462/6048 | |
| dc.description.abstract | Four different derivatives of aromatic sulfonamides have been synthesized: 1,2-bis[(4-sulfonamidobenzamide)ethoxyl]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. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Maik Nauka/Interperiodica | en_US |
| dc.relation.isversionof | 10.1023/A:1020538422592 | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Inhibition | en_US |
| dc.subject | Carbonic Anhydrase | en_US |
| dc.subject | Glaucoma | en_US |
| dc.subject | Sulfanamides | en_US |
| dc.title | Synthesis of new sulfonamide inhibitors of carbonic anhydrase | en_US |
| dc.type | article | en_US |
| dc.relation.journal | Biochemistry-Moscow | en_US |
| dc.contributor.department | Fen Edebiyat Fakültesi | en_US |
| dc.identifier.volume | 67 | en_US |
| dc.identifier.issue | 9 | en_US |
| dc.identifier.startpage | 1055 | en_US |
| dc.identifier.endpage | 1057 | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
