Carbonic anhydrase inhibitors - Part 49: Synthesis of substituted ureido and thioureido derivatives of aromatic/heterocyclic sulfonamides with increased affinities for isozyme I-Reference-Cited by-同舟云学术

Carbonic anhydrase inhibitors - Part 49: Synthesis of substituted ureido and thioureido derivatives of aromatic/heterocyclic sulfonamides with increased affinities for isozyme I

Published:1998-02 Issue:2 Volume:33 Page:83-93
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Supuran Claudiu T.,Scozzafava Andrea,Jurca Bogdan C.,Ilies Marc A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference60 articles.

1. Preceding part of this series: Scozzafava A., Supuran C.T., submitted for publication in J. Enzyme Inhib.

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

3. Expression of Mouse Carbonic Anhydrase VII inE. coliand Demonstration of Its CO2Hydrase Activity

4. Carbonic Anhydrase and Modulation of Physiologic and Pathologic Processes in the Organism;Supuran,1994

5. Sulphanilamide as a Specific Inhibitor of Carbonic Anhydrase

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