A small series of N-glycosylsulfonamides incorporating the phenol moiety has been prepared by Ferrier sulfonamidoglycosylation of D-glycals. N-Glycosides were tested for the inhibition of four isoforms of carbonic anhydrase. In this study, all compounds showed good inhibitory activity against hCA I and II, with selectivity against the cytosolic hCA II versus the tumor associated isozymes. These results confirm that attaching carbohydrate moieties to CA phenol pharmacophore improves and enhances its inhibitory activity.Fil: Riafrecha, Leonardo Ezequiel. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Departamento de Química. Laboratorio de Estudio de Compu...
Carbonic Anhydrases (CAs) are pharmaceutically relevant targets for the treatment of several disease...
The selective inhibition of cancer-associated human carbonic anhydrase (CA) enzymes, specifically CA...
A small series of C-glycosides containing the phenol moiety was tested for the inhibition of the β-c...
One of the most successful approaches for designing carbonic anhydrase (CA, EC 4.2.1.1) inhibitors w...
A small series of C-cinnamoyl glycosides incorporating the phenol moiety has been prepared by reacti...
The synthesis of selective inhibitors of human carbonic anhydrases (hCAs) is of paramount importance...
A general approach for the synthesis of carbonic anhydrases glycoinhibitors belonging to an aminoxys...
The transmembrane isoforms of carbonic anhydrase (CA IX and XII) have been shown to be linked to car...
The transmembrane isoforms of carbonic anhydrase (hCA IX and XII) have been shown to be linked to ca...
A series of arylsulfonamides has been synthesized and investigated for the inhibition of some select...
Carbonic anhydrases (CAs) are metalloenzymes responsible for the reversible hydration of carbon diox...
The selective inhibition of cancer-associated human carbonic anhydrase (CA) enzymes, specifically CA...
A new series of N-heteroarylsubstituted triazolosulfonamide compounds were synthesized and their inh...
A series of 2-(hydrazinocarbonyl)-3-substitutedphenyl-1H-indole-5-sulfonamides possessing various 2-...
Here, we investigate 28 structurally new sulfonamides and their subsequent testing for enzyme inhibi...
Carbonic Anhydrases (CAs) are pharmaceutically relevant targets for the treatment of several disease...
The selective inhibition of cancer-associated human carbonic anhydrase (CA) enzymes, specifically CA...
A small series of C-glycosides containing the phenol moiety was tested for the inhibition of the β-c...
One of the most successful approaches for designing carbonic anhydrase (CA, EC 4.2.1.1) inhibitors w...
A small series of C-cinnamoyl glycosides incorporating the phenol moiety has been prepared by reacti...
The synthesis of selective inhibitors of human carbonic anhydrases (hCAs) is of paramount importance...
A general approach for the synthesis of carbonic anhydrases glycoinhibitors belonging to an aminoxys...
The transmembrane isoforms of carbonic anhydrase (CA IX and XII) have been shown to be linked to car...
The transmembrane isoforms of carbonic anhydrase (hCA IX and XII) have been shown to be linked to ca...
A series of arylsulfonamides has been synthesized and investigated for the inhibition of some select...
Carbonic anhydrases (CAs) are metalloenzymes responsible for the reversible hydration of carbon diox...
The selective inhibition of cancer-associated human carbonic anhydrase (CA) enzymes, specifically CA...
A new series of N-heteroarylsubstituted triazolosulfonamide compounds were synthesized and their inh...
A series of 2-(hydrazinocarbonyl)-3-substitutedphenyl-1H-indole-5-sulfonamides possessing various 2-...
Here, we investigate 28 structurally new sulfonamides and their subsequent testing for enzyme inhibi...
Carbonic Anhydrases (CAs) are pharmaceutically relevant targets for the treatment of several disease...
The selective inhibition of cancer-associated human carbonic anhydrase (CA) enzymes, specifically CA...
A small series of C-glycosides containing the phenol moiety was tested for the inhibition of the β-c...