Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1348672 | Tetrahedron: Asymmetry | 2006 | 6 Pages |
Abstract
Based on the reported glycosidase inhibitory activities of 1,6-dideoxy-1,6-imino-l-iditol, the corresponding aryl glycosides 4-nitrophenyl α- and β-l-idoseptanoside 7 and 8 were synthesised as possible glycosidase substrates. Despite their inherently larger size, these septanosides were indeed shown to be glycosidase substrates, albeit weak ones. In addition, these two substrate analogues 7 and 8 also demonstrated a remarkable degree of selectivity for β- and α-glucosidases, respectively.
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Authors
Andreas Tauss, Andreas J. Steiner, Arnold E. Stütz, Chris A. Tarling, Stephen G. Withers, Tanja M. Wrodnigg,