PMID

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Article Title

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Tricyclic sulfonamides incorporating benzothiopyrano[4,3-c]pyrazole and pyridothiopyrano[4,3-c]pyrazole effectively inhibita- andß-carbonic anhydrase: X-ray crystallography and solution investigations on 15 isoforms.

University of Pisa

Carbonic anhydrase inhibitors. Inhibition of the Rv1284 and Rv3273 beta-carbonic anhydrases from Mycobacterium tuberculosis with diazenylbenzenesulfonamides.

Universita Degli Studi Di Firenze

Inhibition studies of theß-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium with sulfonamides and sulfamates.

Kochi Medical School

Inhibition studies with anions and small molecules of two novel β-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium.

Universita Degli Studi Di Firenze

Natural product-based phenols as novel probes for mycobacterial and fungal carbonic anhydrases.

Griffith University

Inhibition ofß-carbonic anhydrases with ureido-substituted benzenesulfonamides.

Universita Degli Studi Di Firenze

Discovery of low nanomolar and subnanomolar inhibitors of the mycobacterial beta-carbonic anhydrases Rv1284 and Rv3273.

Istanbul University

Inhibition of the ß-class carbonic anhydrases from Mycobacterium tuberculosis with carboxylic acids.

Universit�� Degli Studi Di Firenze

Dihalogenated sulfanilamides and benzolamides are effective inhibitors of the three ß-class carbonic anhydrases from Mycobacterium tuberculosis.

Universit�� Degli Studi Di Firenze

Molecular cloning, characterization, and inhibition studies of the Rv1284 beta-carbonic anhydrase from Mycobacterium tuberculosis with sulfonamides and a sulfamate.

Kochi Medical School