4229-38-3
Chemical Structure
2-(Acetylamino)-2-deoxy-β-D-glucopyranosylamine
- CAS No.: 4229-38-3
- Formula:C8H16N2O5
- Molecular Weight:220.22
IUPAC Name: N-((2R,3R,4R,5S,6R)-2-amino-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide
InChIKey: MCGXOCXFFNKASF-FMDGEEDCSA-N
SMILES: CC(N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1N)CO)O)O)=O
Biological Activity: 2-(Acetylamino)-2-deoxy-β-D-glucopyranosylamine 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. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2-(Acetylamino)-2-deoxy-β-D-glucopyranosylamine | 98.36% | 2-(Acetylamino)-2-deoxy-β-D-glucopyranosylamine 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...
/
|
|||||||||||||||||||||||