| Literature DB >> 22618082 |
M Aguilar-Moncayo1, T Takai, K Higaki, T Mena-Barragán, Y Hirano, K Yura, L Li, Y Yu, H Ninomiya, M I García-Moreno, S Ishii, Y Sakakibara, K Ohno, E Nanba, C Ortiz Mellet, J M García Fernández, Y Suzuki.
Abstract
Competitive inhibitors of either α-galactosidase (α-Gal) or β-galactosidase (β-Gal) with high affinity and selectivity have been accessed by exploiting aglycone interactions with conformationally locked sp(2)-iminosugars. Selected compounds were profiled as potent pharmacological chaperones for mutant lysosomal α- and β-Gal associated with Fabry disease and GM(1) gangliosidosis.Entities:
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Year: 2012 PMID: 22618082 DOI: 10.1039/c2cc32065g
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222