65877-63-6
Chemical Structure
3-O-(Phenylmethyl)-α-D-mannopyranose
- CAS No.: 65877-63-6
- Formula:C13H18O6
- Molecular Weight:270.28
IUPAC Name: (2S,3S,4S,5R,6R)-4-(benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-2,3,5-triol
InChIKey: FYEFQDXXKFUMOJ-BNDIWNMDSA-N
SMILES: O[C@H]([C@H](O[C@@H]([C@H]1O)O)CO)[C@@H]1OCC2=CC=CC=C2
Biological Activity: 3-O-(Phenylmethyl)-α-D-mannopyranose 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
3-O-(Phenylmethyl)-α-D-mannopyranose | 3-O-(Phenylmethyl)-α-D-mannopyranose 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...
/
|
|||||||||||||||||||||||
Keywords