Inhibition studies of Brucella suis β-carbonic anhydrases with a series of 4-substituted pyridine-3-sulphonamides

por Monti, Simona Maria, Meccariello, Angela, Ceruso, Mariangela, Szafrański, Krzysztof, Sławiński, Jarosław, Supuran, Claudiu T.
Publicado 2017

Aryl-4,5-dihydro-1H-pyrazole-1-carboxamide Derivatives Bearing a Sulfonamide Moiety Show Single-digit Nanomolar-to-Subnanomolar Inhibition Constants against the Tumor-associated Hu...

por Hargunani, Priya, Tadge, Nikhil, Ceruso, Mariangela, Leitans, Janis, Kazaks, Andris, Tars, Kaspars, Gratteri, Paola, Supuran, Claudiu T., Nocentini, Alessio, Toraskar, Mrunmayee P.
Publicado 2020

Open saccharin-based secondary sulfonamides as potent and selective inhibitors of cancer-related carbonic anhydrase IX and XII isoforms

por D’Ascenzio, Melissa, Guglielmi, Paolo, Carradori, Simone, Secci, Daniela, Florio, Rosalba, Mollica, Adriano, Ceruso, Mariangela, Akdemir, Atilla, Sobolev, Anatoly P., Supuran, Claudiu T.
Publicado 2016

Inhibition of the α-carbonic anhydrase from Vibrio cholerae with amides and sulfonamides incorporating imidazole moieties

por De Vita, Daniela, Angeli, Andrea, Pandolfi, Fabiana, Bortolami, Martina, Costi, Roberta, Di Santo, Roberto, Suffredini, Elisabetta, Ceruso, Mariangela, Del Prete, Sonia, Capasso, Clemente, Scipione, Luigi, Supuran, Claudiu T.
Publicado 2017