13343-64-1
Chemical Structure
Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 3-acetate
- CAS No.: 13343-64-1
- Formula:C24H27NO7
- Molecular Weight:441.47
IUPAC Name: (4aR,6S,7R,8R,8aS)-7-acetamido-6-(benzyloxy)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-8-yl acetate
InChIKey: LXRHDLGFMYNIGA-AUQUAXPWSA-N
SMILES: CC(O[C@H]1[C@@]2([H])[C@](COC(C3=CC=CC=C3)O2)([H])O[C@@H]([C@@H]1NC(C)=O)OCC4=CC=CC=C4)=O
Biological Activity: Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 3-acetate 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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Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 3-acetate | Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 3-acetate 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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