| Literature DB >> 29795760 |
Andrea Angeli1, Lorenzo di Cesare Mannelli2, Elena Trallori2, Thomas S Peat3, Carla Ghelardini2, Fabrizio Carta1, Claudiu T Supuran1.
Abstract
A series of novel selenides bearing benzenesulfonamide moieties was synthesized and investigated for their inhibition on six human (h) carbonic anhydrase (CA, EC 4.2.1.1) isoforms such as the physiologically relevant hCA I, II, VA, VB, VII, and IX and the X-ray complex in adduct with hCA II for some of them investigated. These enzymes are involved in a variety of diseases including glaucoma, retinitis pigmentosa, epilepsy, arthritis, metabolic disorders, and cancer. The investigated compounds showed potent inhibitory action against hCA VA, VII, and IX, in the low nanomolar range, thus making them of interest for the development of isoform-selective inhibitors and as candidates for various biomedical applications.Entities:
Year: 2018 PMID: 29795760 PMCID: PMC5949733 DOI: 10.1021/acsmedchemlett.8b00076
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345