33639-80-4

2-Acetamido-2-deoxy-6-O-(α-L-fucopyranosyl)-D-glucopyranose Chemical Structure
33639-80-4

Chemical Structure

2-Acetamido-2-deoxy-6-O-(α-L-fucopyranosyl)-D-glucopyranose

  • CAS No.: 33639-80-4
  • Formula:C14H25NO10
  • Molecular Weight:367.35

IUPAC Name: N-((3R,4R,5S,6R)-2,4,5-trihydroxy-6-((((2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-3-yl)acetamide

InChIKey: BSNVYGSAFLBSSQ-PKAYUKAWSA-N

SMILES: O[C@@H]([C@@H]([C@@H]([C@@H](O1)C)O)O)[C@@H]1OC[C@@H]2[C@H]([C@@H]([C@H](C(O2)O)NC(C)=O)O)O

Biological Activity: 2-Acetamido-2-deoxy-6-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].

Cat. No. Product Name Purity Description Pricing
HY-W353880
2-Acetamido-2-deoxy-6-O-(α-L-fucopyranosyl)-D-glucopyranose 2-Acetamido-2-deoxy-6-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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