Carbonic anhydrase inhibitors. Part 43. Schiff bases derived from aromatic sulfonamides: towards more specific inhibitors for membrane-bound versus cytosolic isozymes
- 1 May 1997
- journal article
- research article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 32 (5) , 445-452
- https://doi.org/10.1016/s0223-5234(97)81681-9
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Carbonic anhydrase inhibitors. Part 35. Synthesis of Schiff bases derived from sulfanilamide and aromatic aldehydes: the first inhibitors with equally high affinity towards cytosolic and membrane-bound isozymesEuropean Journal of Medicinal Chemistry, 1996
- Carbonic anhydrase inhibitors: Synthesis and inhibitory properties of 1,3,4-thiadiazole-2,5-bissulfonamideEuropean Journal of Medicinal Chemistry, 1996
- Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucomaJournal of Medicinal Chemistry, 1989
- The carbonic anhydrases: Widening perspectives on their evolution, expression and functionBioEssays, 1989
- Carbonic anhydrase: General perspective and advances in glaucoma researchDrug Development Research, 1987
- Acute mountain sickness and acetazolamide. Clinical efficacy and effect on ventilationJAMA, 1982
- Carbonic anhydrase: chemistry, physiology, and inhibitionPhysiological Reviews, 1967
- Carbonic Anhydrase Inhibitors. I. Benzothiazole DerivativesThe Journal of Organic Chemistry, 1958
- Stucture and Chemotherapeutic Activities of Sulfanilamide Derivatives.Chemical Reviews, 1940
- Sulphanilamide as a Specific Inhibitor of Carbonic AnhydraseNature, 1940