7368-73-2
Chemical Structure
2-O-α-D-Glucopyranosyl-D-galactose
- CAS No.: 7368-73-2
- Formula:C12H22O11
- Molecular Weight:342.30
IUPAC Name: (2R,3S,4S,5R)-3,4,5,6-tetrahydroxy-2-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal
InChIKey: PZDOWFGHCNHPQD-IJVVWVSMSA-N
SMILES: OC[C@@H](O)[C@H](O)[C@H](O)[C@H](C=O)O[C@H]1O[C@@H]([C@H]([C@@H]([C@H]1O)O)O)CO
Biological Activity: 2-O-α-D-Glucopyranosyl-D-galactose 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-O-α-D-Glucopyranosyl-D-galactose | 2-O-α-D-Glucopyranosyl-D-galactose 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