52630-68-9
Chemical Structure
2-Acetamido-2-deoxy-3-O-(α-L-fucopyranosyl)-D-glucopyranose
- CAS No.: 52630-68-9
- Formula:C14H25NO10
- Molecular Weight:367.35
IUPAC Name: N-((2R,3R,4R,5R)-4,5,6-trihydroxy-1-oxo-3-(((2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)hexan-2-yl)acetamide
InChIKey: YDWJUIXDZSJZHH-MYCHVAHWSA-N
SMILES: CC(N[C@@H](C=O)[C@H]([C@H](O)[C@H](O)CO)O[C@H]1[C@H]([C@@H]([C@@H]([C@@H](O1)C)O)O)O)=O
Biological Activity: 2-Acetamido-2-deoxy-3-O-(α-L-fucopyranosyl)-D-glucopyranose 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-Acetamido-2-deoxy-3-O-(α-L-fucopyranosyl)-D-glucopyranose | 2-Acetamido-2-deoxy-3-O-(α-L-fucopyranosyl)-D-glucopyranose 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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