| Literature DB >> 25815148 |
Muhammet Tanc1, Fabrizio Carta2, Andrea Scozzafava2, Claudiu T Supuran1.
Abstract
The α-carbonic anhydrases (CAs, EC 4.2.1.1) show catalytic versatility acting as esterases with carboxylic, sulfonic, and phosphate esters. Here we prove by kinetic, spectroscopic, and MS studies that they also possess thioesterase activity with a dithiocarbamate ester as a substrate (PhSO2NHCSSMe). Its CA-mediated hydrolysis leads to benzenesulfonamide, methyl mercaptan, and COS. The CA thioesterase activity may be useful for designing prodrug enzyme inhibitors, whereas some CA isoforms may use this activity for modulating physiologic/pathologic processes, which are possibly amenable to drug discovery of agents with multiple mechanisms of action.Entities:
Keywords: Carbonic anhydrase; inhibitors; prodrugs; thioesterase
Year: 2015 PMID: 25815148 PMCID: PMC4360143 DOI: 10.1021/ml500470b
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345