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Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of N-substituted benzenesulfonamides to human isoform II†
Anna Di Fiore,Alfonso Maresca,Vincenzo Alterio,Claudiu T. Supuran,Giuseppina De Simone
Chemical Communications Pub Date : 09/26/2011 00:00:00 , DOI:10.1039/C1CC14575D
Abstract

N-substituted benzenesulfonamides, incorporating the N-amino-, N-hydroxy- and N-methoxy-moieties at the sulfonamide zinc binding group, have been investigated as CAIs by means of inhibition and structural studies, unraveling interesting aspects related to their inhibition mechanism.

Graphical abstract: Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of N-substituted benzenesulfonamides to human isoform II
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