J. Enzyme Inhib. Med. Chem. 2016, 31 (6), 1707-1711
DOI: 10.3109/14756366.2016.1156676
Krasavin M.; Stavniichuk R.; Zozulya S.; Borysko P.; Vullo D.; Supuran C. T.
A new type of carbonic anhydrase inhibitors was identified via differential scanning fluorimetry (DSF) screening. The compounds displayed interesting inhibition profile against human carbonic anhydrase isoforms I, II, IX and XII with an obvious selectivity displayed by one compound toward carbonic anhydrase (CA) IX, an established anti-cancer target. A hypothetical mechanism of inhibitory action by the Strecker-type α-aminonitriles has been proposed.