4515-24-6
Chemical Structure
2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranosylamine
- CAS No.: 4515-24-6
- Formula:C14H22N2O8
- Molecular Weight:346.33
IUPAC Name: (2R,3S,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-aminotetrahydro-2H-pyran-3,4-diyl diacetate
InChIKey: DKGKXBJJPLBTOQ-DHGKCCLASA-N
SMILES: CC(O[C@H]1[C@@H]([C@H](O[C@H]([C@@H]1NC(C)=O)N)COC(C)=O)OC(C)=O)=O
Biological Activity: 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-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. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranosylamine | 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-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...
/
|
|||||||||||||||||||||||