29847-23-2
Chemical Structure
2-Acetamido-2-deoxy-β-D-glucopyranosyl azide
- CAS No.: 29847-23-2
- Formula:C8H14N4O5
- Molecular Weight:246.22
IUPAC Name: N-((2R,3R,4R,5S,6R)-2-azido-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide
InChIKey: CCZCDCDASZJFGK-FMDGEEDCSA-N
SMILES: CC(N[C@H]1[C@@H](O[C@@H]([C@H]([C@@H]1O)O)CO)N=[N+]=[N-])=O
Biological Activity: 2-Acetamido-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].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2-Acetamido-2-deoxy-β-D-glucopyranosyl azide | 2-Acetamido-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. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
