| Literature DB >> 28548311 |
Dimitri Alvarez-Dorta1, Dustin T King2, Thibaut Legigan3, Daisuke Ide4, Isao Adachi4, David Deniaud1, Jérôme Désiré3, Atsushi Kato4, David Vocadlo2, Sébastien G Gouin1, Yves Blériot3.
Abstract
A set of multivalent polyhydroxylated acetamidoazepanes based on ethylene glycol, glucoside, or cyclodextrin scaffolds was prepared. The compounds were assessed against plant, mammalian, and therapeutically relevant hexosaminidases. Multimerization was shown to improve the inhibitory potency with synergy, and to fine tune the selectivity profile between related hexosaminidases.Entities:
Keywords: exo-N-acetyl-β-glucosaminidases; glycoclusters; glycosidases; iminosugars; multivalency
Mesh:
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Year: 2017 PMID: 28548311 DOI: 10.1002/chem.201701756
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236