65730-00-9

2-Propen-1-yl 2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-β-D-glucopyranoside Chemical Structure
65730-00-9

Chemical Structure

2-Propen-1-yl 2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-β-D-glucopyranoside

  • CAS No.: 65730-00-9
  • Formula:C18H25NO6
  • Molecular Weight:351.39

IUPAC Name: N-((2R,3R,4R,5S,6R)-2-(allyloxy)-4-(benzyloxy)-5-hydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide

InChIKey: RRZBCUVUJQCHIM-DUQPFJRNSA-N

SMILES: CC(N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1OCC=C)CO)O)OCC2=CC=CC=C2)=O

Biological Activity: 2-Propen-1-yl 2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-β-D-glucopyranoside 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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HY-W700582
2-Propen-1-yl 2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-β-D-glucopyranoside 2-Propen-1-yl 2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-β-D-glucopyranoside 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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