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SHR Neuro Cancer Cardio Lipid Metab Microb

Yu, H; Lau, K; Thon, V; Autran, CA; Jantscher-Krenn, E; Xue, M; Li, Y; Sugiarto, G; Qu, J; Mu, S; Ding, L; Bode, L; Chen, X.
Synthetic disialyl hexasaccharides protect neonatal rats from necrotizing enterocolitis.
Angew Chem Int Ed Engl. 2014; 53(26):6687-6691 Doi: 10.1002/anie.201403588 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-authors Med Uni Graz
Jantscher-Krenn Evelyn
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Abstract:
Two novel synthetic α2-6-linked disialyl hexasaccharides, disialyllacto-N-neotetraose (DSLNnT) and α2-6-linked disialyllacto-N-tetraose (DS'LNT), were readily obtained by highly efficient one-pot multienzyme (OPME) reactions. The sequential OPME systems described herein allowed the use of an inexpensive disaccharide and simple monosaccharides to synthesize the desired complex oligosaccharides with high efficiency and selectivity. DSLNnT and DS'LNT were shown to protect neonatal rats from necrotizing enterocolitis (NEC) and are good therapeutic candidates for preclinical experiments and clinical application in treating NEC in preterm infants. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Bifidobacterium - enzymology
Drug Evaluation, Preclinical -
Enterocolitis, Necrotizing - drug therapy
Multienzyme Complexes - metabolism
Oligosaccharides - chemical synthesis
Oligosaccharides - chemistry
Oligosaccharides - therapeutic use
Protective Agents - chemical synthesis
Protective Agents - chemistry
Protective Agents - therapeutic use
Rats -

Find related publications in this database (Keywords)
disialyl glycans
enzymatic synthesis
enzymes
necrotizing enterocolitis
oligosaccharides
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