Carbonic anhydrase activators. Part 14. Syntheses of mono and bis pyridinium salt derivatives of 2-amino-5-(2-aminoethyl)- and 2-amino-5-(3-aminopropyl)-1,3,4-thiadiazole and their interaction with isozyme II
- 1 January 1996
- journal article
- Published by Elsevier BV in European Journal of Medicinal Chemistry
- Vol. 31 (7-8), 597-606
- https://doi.org/10.1016/0223-5234(96)89555-9
Abstract
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This publication has 11 references indexed in Scilit:
- Carbonic anhydrase inhibitors. Part 24. A quantitative structure-activity relationship study of positively charged sulfonamide inhibitorsEuropean Journal of Medicinal Chemistry, 1995
- Carbonic Anhydrase Activators. 3: Structure-Activity Correlations for a Series of Isozyme I1 ActivatorsJournal of Pharmaceutical Sciences, 1994
- Carbonic Anhydrase Inhibitors. V: Pyrylium Salts in the Synthesis of Isozyme-Specific InhibitorsJournal of Pharmaceutical Sciences, 1992
- The pharmacology of antiglaucoma drugsPharmacology & Therapeutics, 1989
- The catalytic mechanism of carbonic anhydrase: implications of a rate-limiting protolysis of waterAccounts of Chemical Research, 1988
- Treatment of Gastroduodenal Ulcers with Carbonic Anhydrase InhibitorsAnnals of the New York Academy of Sciences, 1984
- Carbonic anhydrase: chemistry, physiology, and inhibitionPhysiological Reviews, 1967
- 1,2,4-Triazole Analogs of HistamineJournal of the American Chemical Society, 1953
- Studies on 1, 3, 4-Thiadiazole Derivatives. VIYAKUGAKU ZASSHI, 1952
- Über einige synthetisch verwertbare Derivate der AminosäurenEuropean Journal of Inorganic Chemistry, 1908