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Topically active carbonic anhydrase inhibitors. 3. Benzofuran- and indole-2-sulfonamides.
Graham, S L; Hoffman, J M; Gautheron, P; Michelson, S R; Scholz, T H; Schwam, H; Shepard, K L; Smith, A M; Smith, R L; Sondey, J M.
Affiliation
  • Graham SL; Department of Medicinal Chemistry, Merck Sharp and Dohme Research Laboratories, West Point, Pennsylvania 19486.
J Med Chem ; 33(2): 749-54, 1990 Feb.
Article in En | MEDLINE | ID: mdl-2299640
Derivatives of benzofuran- and indole-2-sulfonamide were prepared for evaluation as topically active ocular hypotensive agents. These compounds were found to be excellent inhibitors of carbonic anhydrase and to lower intraocular pressure in a rabbit model of ocular hypertension. However, the development of these compounds for clinical use was precluded by the observation that they cause dermal sensitization in guinea pigs. A correlation between electrophilicity, as assessed by in vitro reactivity with reduced glutathione, and dermal sensitization potential was further documented.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Carbonic Anhydrase Inhibitors Limits: Animals Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 1990 Document type: Article Country of publication: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Carbonic Anhydrase Inhibitors Limits: Animals Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 1990 Document type: Article Country of publication: United States