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Anomer-selective inhibition of glycosidases using aminocyclopentanols.
Leroy, E; Reymond, J L.
Afiliação
  • Leroy E; Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland.
Org Lett ; 1(5): 775-7, 1999 Sep 09.
Article em En | MEDLINE | ID: mdl-10823203
[reaction: see text] (1S,2S,3S,4R,5R)-4-amino-5-(hydroxymethyl)cyclopentane-1,2,3-triol 1 is prepared stereoselectively from D-lyxose and displays anomer-selective inhibition for beta-galactosidase (Ki = 3.0 x 10(-6) M) and beta-glucosidase (Ki = 1.5 x 10(-7) M), over alpha-galactosidase (Ki = 2.3 x 10(-5) M) and alpha-glucosidase (IC50 = 1.0 x 10(-4) M). There is no observable cross-reactivity with alpha-mannosidase, beta-mannosidase, or alpha-L-fucosidase.
Assuntos
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Base de dados: MEDLINE Assunto principal: Ciclopentanos / Inibidores Enzimáticos / Glicosídeo Hidrolases Idioma: En Ano de publicação: 1999 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Ciclopentanos / Inibidores Enzimáticos / Glicosídeo Hidrolases Idioma: En Ano de publicação: 1999 Tipo de documento: Article