International audience; A series of benzofused sultams and fluorinated benzenesulfonamides were synthesized in superacid HF/SbF5 from simple N-allylic derivatives. Almost all of these original compounds showed micromolar inhibitory activities against carbonic anhydrases I and II. The fluorinated derivatives inhibit better the tumor-associated isoforms IX and XII, and one of the tested compounds showed inhibition in the nanomolar range
Pursuing on our efforts toward searching for efficient hCA IX and hCA XII inhibitors, herein we repo...
Herein we report on a new series of hydrazidoureidobenzensulfonamides investigated as inhibitors of ...
A diverse set of mono- and bis-sulfonamide was obtained via a direct, chemoselective sulfochlorinati...
International audienceA series of benzofused sultams and fluorinated benzenesulfonamides were synthe...
International audienceA series of tertiary (fluorinated) benzenesulfonamides was synthesized in supe...
International audienceTertiary substituted (fluorinated) benzenesulfonamides were synthesized in sup...
International audienceA series of new, halogen containing N-substituted 4-aminobenzenesulfonamides w...
A series of new thienyl-substituted pyrazoline benzenesulfonamides were synthesized and their carbon...
A set of sulfamides and sulfamates were synthesized and tested against several isoforms of carbonic ...
The inhibition of two human cytosolic carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I, II and human ...
Benzenesulfonamides bearing various substituted (hetero)aryl rings in the para-position were prepare...
A series of novel benzene- and 2,3,5,6-tetrafluorobenzenesulfonamide was synthesized by using a clic...
A small series of hydrazonobenzenesulfonamides was designed, synthesized and studied for their human...
As a part of our efforts to expand chemical diversity in the carbonic anhydrases inhibitors (CAIs), ...
N-protected amino acids (Gly, Ala and Phe protected with Boc and Z groups) were reacted with sulfona...
Pursuing on our efforts toward searching for efficient hCA IX and hCA XII inhibitors, herein we repo...
Herein we report on a new series of hydrazidoureidobenzensulfonamides investigated as inhibitors of ...
A diverse set of mono- and bis-sulfonamide was obtained via a direct, chemoselective sulfochlorinati...
International audienceA series of benzofused sultams and fluorinated benzenesulfonamides were synthe...
International audienceA series of tertiary (fluorinated) benzenesulfonamides was synthesized in supe...
International audienceTertiary substituted (fluorinated) benzenesulfonamides were synthesized in sup...
International audienceA series of new, halogen containing N-substituted 4-aminobenzenesulfonamides w...
A series of new thienyl-substituted pyrazoline benzenesulfonamides were synthesized and their carbon...
A set of sulfamides and sulfamates were synthesized and tested against several isoforms of carbonic ...
The inhibition of two human cytosolic carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I, II and human ...
Benzenesulfonamides bearing various substituted (hetero)aryl rings in the para-position were prepare...
A series of novel benzene- and 2,3,5,6-tetrafluorobenzenesulfonamide was synthesized by using a clic...
A small series of hydrazonobenzenesulfonamides was designed, synthesized and studied for their human...
As a part of our efforts to expand chemical diversity in the carbonic anhydrases inhibitors (CAIs), ...
N-protected amino acids (Gly, Ala and Phe protected with Boc and Z groups) were reacted with sulfona...
Pursuing on our efforts toward searching for efficient hCA IX and hCA XII inhibitors, herein we repo...
Herein we report on a new series of hydrazidoureidobenzensulfonamides investigated as inhibitors of ...
A diverse set of mono- and bis-sulfonamide was obtained via a direct, chemoselective sulfochlorinati...