53167-38-7
Chemical Structure
Gal1-β-4GlcNAc-β-Bn
Synonym(s): Benzyl β-D-galactopyranosyl-(1→4)-β-D-N-acetylglucosamine
- CAS No.: 53167-38-7
- Formula:C21H31NO11
- Molecular Weight:473.47
IUPAC Name: N-((2R,3R,4R,5S,6R)-2-(benzyloxy)-4-hydroxy-6-(hydroxymethyl)-5-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-3-yl)acetamide
InChIKey: SYUTXOZIXYNPMH-VSPFHFLJSA-N
SMILES: OC[C@@H](O[C@H]([C@@H]([C@H]1O)NC(C)=O)OCC2=CC=CC=C2)[C@H]1O[C@@H]3O[C@@H]([C@@H]([C@@H]([C@H]3O)O)O)CO
Biological Activity: Gal1-β-4GlcNAc-β-Bn (Benzyl β-D-galactopyranosyl-(1→4)-β-D-N-acetylglucosamine) is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].
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Gal1-β-4GlcNAc-β-Bn | Gal1-β-4GlcNAc-β-Bn (Benzyl β-D-galactopyranosyl-(1→4)-β-D-N-acetylglucosamine) is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology. | |||||||||||||||||||||
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Keywords
