Topically active carbonic anhydrase inhibitors. 4. [(Hydroxyalkyl)sulfonyl]benzene and [(hydroxyalkyl)sulfonyl]thiophenesulfonamides

J Med Chem. 1991 Oct;34(10):3098-105. doi: 10.1021/jm00114a020.

Abstract

For several decades a tantalizing goal for the treatment of primary open-angle glaucoma has been the development of a topically active carbonic anhydrase inhibitor. Recent results from several research groups indicate that considerable progress has been made toward this objective. In this report, we present the design and synthesis of (hydroxyalkyl)sulfonyl-substituted benzene- and thiophenesulfonamides. These compounds exhibit inhibition of carbonic anhydrase II in the nanomolar range and lower intraocular pressure in the alpha-chymotrypsinized rabbit model of ocular hypertension after topical instillation.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Topical
  • Animals
  • Benzenesulfonamides
  • Carbonic Anhydrase Inhibitors / chemical synthesis*
  • Carbonic Anhydrase Inhibitors / pharmacology
  • Chymotrypsin
  • Glutathione / metabolism
  • Intraocular Pressure / drug effects
  • Ocular Hypertension / chemically induced
  • Ocular Hypertension / drug therapy
  • Rabbits
  • Structure-Activity Relationship
  • Sulfonamides / chemical synthesis*
  • Sulfonamides / chemistry*
  • Sulfonamides / pharmacology
  • Sulfonamides / therapeutic use
  • Thiophenes / chemical synthesis*
  • Thiophenes / pharmacology
  • Thiophenes / therapeutic use

Substances

  • Carbonic Anhydrase Inhibitors
  • Sulfonamides
  • Thiophenes
  • Chymotrypsin
  • Glutathione