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Journal of Medicinal Chemistry|February 1, 1988
(Acyloxy)alkyl carbamates as novel bioreversible prodrugs for amines: increased permeation through biological membranesJ Alexander, R Cargill, S R Michelson, et al.Biochemical and Biophysical Research Communications|November 15, 1989
Affinity purification of the HIV-1 proteaseJ C Heimbach, V M Garsky, S R Michelson, et al.Journal of Medicinal Chemistry|January 21, 1994
3-substituted thieno[2,3-b][1,4]thiazine-6-sulfonamides. A novel class of topically active carbonic anhydrase inhibitorsC A Hunt, P J Mallorga, S R Michelson, et al.The Journal of Pharmacology and Experimental Therapeutics|July 1, 1995
Time- and dose-dependent pharmacokinetics of L-754,394, an HIV protease inhibitor, in rats, dogs and monkeysJ H Lin, M Chiba, I W Chen, et al.Journal of Medicinal Chemistry|October 16, 1992
4-substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitorsG D Hartman, W Halczenko, R L Smith, et al.Journal of Medicinal Chemistry|August 7, 1992
Thieno[2,3-b]furan-2-sulfonamides as topical carbonic anhydrase inhibitorsG D Hartman, W Halczenko, J D Prugh, et al.Journal of Medicinal Chemistry|August 1, 1983
Inhibitors of glycolic acid oxidase. 4-substituted 2,4-dioxobutanoic acid derivativesH W Williams, E Eichler, W C Randall, et al.Journal of Medicinal Chemistry|June 1, 1979
Quantitative structure-activity relationships involving the inhibition of glycolic acid oxidase by derivatives of glycolic and glyoxylic acidsW C Randall, K B Streeter, E L Cresson, et al.Journal of Medicinal Chemistry|February 1, 1990
Topically active carbonic anhydrase inhibitors. 3. Benzofuran- and indole-2-sulfonamidesS L Graham, J M Hoffman, P Gautheron, et al.Journal of Medicinal Chemistry|October 1, 1991
Topically active carbonic anhydrase inhibitors. 4. [(Hydroxyalkyl)sulfonyl]benzene and [(hydroxyalkyl)sulfonyl]thiophenesulfonamidesK L Shepard, S L Graham, R J Hudcosky, et al.Pageof 2