A straightforward access to TMG-chitooligomycins and their evaluation as β-N-acetylhexosaminidase inhibitors.
In: Carbohydrate research, Jg. 368 (2013-03-07), S. 52
Online
academicJournal
Zugriff:
A chemo-biotechnological approach is reported for the synthesis of TMG-chitooligomycins, CO-n (NMe(3)). Their abilities to inhibit β-N-acetylhexosaminidases (HexNAcases), from Aspergillus oryzae (AoHex, fungi), Canavalia ensiformis (CeHex, plant) HexNAcases and a chitobiase from Serratia marcescens (SmCHB, bacteria) were studied and compared with their precursors CO-n (N). CO-n (NMe(3)) were revealed as potent inhibitors for AoHex and SmCHB with a proved chain length effect while CO-n (N) was a highly selective inhibitor of SmCHB. This route can be considered as the privileged way to produce easily and in large scale a wide range of size-defined chitooligosaccharide-based inhibitors to fine-tune the structure-activity relationships for inhibition of HexNAcases from various origins.
(Copyright © 2012 Elsevier Ltd. All rights reserved.)
Titel: |
A straightforward access to TMG-chitooligomycins and their evaluation as β-N-acetylhexosaminidase inhibitors.
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Autor/in / Beteiligte Person: | Halila, S ; Samain, E ; Vorgias, CE ; Armand, S |
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Zeitschrift: | Carbohydrate research, Jg. 368 (2013-03-07), S. 52 |
Veröffentlichung: | Amsterdam : Elsevier ; <i>Original Publication</i>: Amsterdam., 2013 |
Medientyp: | academicJournal |
ISSN: | 1873-426X (electronic) |
DOI: | 10.1016/j.carres.2012.12.007 |
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