| Literature DB >> 28302505 |
Andrea Angeli1, Damiano Tanini2, Caterina Viglianisi2, Lucia Panzella3, Antonella Capperucci2, Stefano Menichetti2, Claudiu T Supuran4.
Abstract
A series of selenides, diselenides and organoselenoheterocycles were evaluated as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors against the human (h) isoforms hCA I, II, IV, VII and IX, involved in a variety of diseases among which glaucoma, retinitis pigmentosa, epilepsy, arthritis and tumors etc. These investigated compounds showed inhibitory action against these isoforms and some of them were selective for inhibiting the cytosolic over the membrane-bound isoforms, thus making them interesting leads for the development of isoform-selective inhibitors.Entities:
Keywords: Carbonic anhydrase; Diselenides; Inhibitors; Metalloenzymes; Selenides; Selenium; Selenoheterocycles
Mesh:
Substances:
Year: 2017 PMID: 28302505 DOI: 10.1016/j.bmc.2017.03.013
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641