| Literature DB >> 23503420 |
Benoît Métayer1, Agnès Mingot, Daniella Vullo, Claudiu T Supuran, Sébastien Thibaudeau.
Abstract
Tertiary substituted (fluorinated) benzenesulfonamides were synthesized in superacid HF/SbF5 and tested as inhibitors of human carbonic anhydrases (hCAs, EC 4.2.1.1). Strong selectivity toward tumor-associated hCA IX, without inhibiting the offtarget hCA II, was observed, pointing out to a new mechanism of action compared to classical sulfonamides.Entities:
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Year: 2013 PMID: 23503420 DOI: 10.1039/c3cc40858b
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222