Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1374924 | Bioorganic & Medicinal Chemistry Letters | 2006 | 4 Pages |
Abstract
1,5-Dideoxy-1,5-iminoalditols of various configurations as well as isofagomine were N-alkylated with non-polar straight chain spacer-arms by a set of simple standard procedures. The spacer-arms’ terminal functional groups, primary amines, were employed to introduce fluorescent tags such as dansyl and dapoxyl moieties. Resulting derivatives in the d-xylo, d-gluco, d-galacto as well as GlcNAc series showed distinctly improved glycosidase inhibitory activities compared to parent compounds and are designed to be useful analytical tools.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Peter Greimel, Herwig Häusler, Inge Lundt, Karen Rupitz, Arnold E. Stütz, Chris A. Tarling, Stephen G. Withers, Tanja M. Wrodnigg,