Carbonic Anhydrase Inhibitors:  Synthesis of Membrane-Impermeant Low Molecular Weight Sulfonamides Possessing in Vivo Selectivity for the Membrane-Bound versus Cytosolic Isozymes

Author:

Scozzafava Andrea1,Briganti Fabrizio1,Ilies Marc A.1,Supuran Claudiu T.1

Affiliation:

1. Laboratorio di Chimica Inorganica e Bioinorganica, Università degli Studi, Via Gino Capponi 7, I-50121 Florence, Italy, and Department of Chemistry, Faculty of Biotechnologies, University of Agricultural Sciences and Veterinary Medicine, B-dul Marasti nr. 59, 71331 Bucharest, Romania

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Reference66 articles.

1. This paper is part 83 of the series. Preceding part:  Renzi, G.; Scozzafava, A.; Supuran, C. T. Carbonic anhydrase inhibitors. Part 82. Topical sulfonamide antiglaucoma agents incorporating secondary amine moieties.Bioorg.Med. Chem. Lett.1999, in press.

2. Functional Diversity, Conservation, and Convergence in the Evolution of the α-, β-, and γ-Carbonic Anhydrase Gene Families

3. Carbonic anhydrase: General perspective and advances in glaucoma research

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