Journal of Medicinal Chemistry p. 3098 - 3105 (1991)
Update date:2022-08-03
Topics:
Shepard
Graham
Hudcosky
Michelson
Scholz
Schwam
Smith
Sondey
Strohmaier
Smith
Sugrue
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 α-chymotrypsinized rabbit model of ocular hypertension after topical instillation.
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