55637-63-3
Chemical Structure
2-(Acetylamino)-2-deoxy-4-O-β-D-mannopyranosyl-D-glucose
- CAS No.: 55637-63-3
- Formula:C14H25NO11
- Molecular Weight:383.35
IUPAC Name: N-((2R,3R,4S,5R)-3,5,6-trihydroxy-1-oxo-4-(((2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexan-2-yl)acetamide
InChIKey: HESSGHHCXGBPAJ-WMSNIUQZSA-N
SMILES: CC(N[C@@H](C=O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@@H]1O[C@@H]([C@H]([C@@H]([C@@H]1O)O)O)CO)=O
Biological Activity: 2-(Acetylamino)-2-deoxy-4-O-β-D-mannopyranosyl-D-glucose 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].
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2-(Acetylamino)-2-deoxy-4-O-β-D-mannopyranosyl-D-glucose | 98.0% | 2-(Acetylamino)-2-deoxy-4-O-β-D-mannopyranosyl-D-glucose 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. | ||||||||||||||||||||
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