19411-48-4Relevant articles and documents
Amido/ureidosubstituted benzenesulfonamides-isatin conjugates as low nanomolar/subnanomolar inhibitors of the tumor-associated carbonic anhydrase isoform XII
Eldehna, Wagdy M.,Fares, Mohamed,Ceruso, Mariangela,Ghabbour, Hazem A.,Abou-Seri, Sahar M.,Abdel-Aziz, Hatem A.,Abou El Ella, Dalal A.,Supuran, Claudiu T.
, p. 259 - 266 (2016)
By using a molecular hybridization approach, two series of amido/ureidosubstituted benzenesulfonamides incorporating substituted-isatin moieties were synthesized. The prepared derivatives were in vitro evaluated for their inhibitory activity against human
Synthesis of novel acridine and bis acridine sulfonamides with effective inhibitory activity against the cytosolic carbonic anhydrase isoforms II and VII
Ulus, Ramazan,Yesildag, Ibrahim,Tanc, Muhammet,Buelbuel, Metin,Kaya, Muharrem,Supuran, Claudiu T.
, p. 5799 - 5805 (2013/09/12)
4-Amino-N-(4-sulfamoylphenyl)benzamide was synthesized by reduction of 4-nitro-N-(4-sulfamoylphenyl)benzamide and used to synthesize novel acridine sulfonamide compounds, by a coupling reaction with cyclic-1,3-diketones and aromatic aldehydes. The new com