80887-27-0
Chemical Structure
2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl azide
- CAS No.: 80887-27-0
- Formula:C22H24N4O5
- Molecular Weight:424.45
IUPAC Name: N-((4aR,6R,7R,8R,8aS)-6-azido-8-(benzyloxy)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)acetamide
InChIKey: FVNJPKGJMMREOM-CGFCOLRFSA-N
SMILES: [N-]=[N+]=N[C@@H]([C@@H]1NC(C)=O)O[C@@](COC(C2=CC=CC=C2)O3)([H])[C@]3([H])[C@@H]1OCC4=CC=CC=C4
Biological Activity: 2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl azide 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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2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl azide | 2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl azide 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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