| Literature DB >> 28728897 |
Marta Ferraroni1, Laura Lucarini2, Emanuela Masini2, Mikhail Korsakov3, Andrea Scozzafava4, Claudiu T Supuran5, Mikhail Krasavin6.
Abstract
Two lead 1,3-oxazole-based carbonic anhydrase inhibitors (CAIs) earlier identified as selective, picomolar inhibitors of hCA II (a cytosolic target for treatment of glaucoma) have been investigated further. Firstly, they were found to be conveniently synthesized on multigram scale, which enables further development. These compounds were found to be comparable in efficacy to dorzolamide eye drops when applied in the eye drop form as well. Finally, the reasons for unusually high potency of these compounds became understood from their high-resolution X-ray crystallography structures. These data significantly expand our understanding of heterocycle-based primary sulfonamides, many of which have recently emerged from our labs - particularly, from the corneal permeability standpoint.Entities:
Keywords: Carbonic anhydrase inhibitors; Isoform selectivity; Multigram synthesis; Ocular hypertension; Picomolar inhibition; Primary sulfonamide; X-ray crystallography
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Year: 2017 PMID: 28728897 DOI: 10.1016/j.bmc.2017.06.054
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641