730911-70-3

Benzyl N-acetyl-4,6-O-benzylidene-α-isomuramic acid Chemical Structure
730911-70-3

Chemical Structure

Benzyl N-acetyl-4,6-O-benzylidene-α-isomuramic acid

  • CAS No.: 730911-70-3
  • Formula:C25H29NO8
  • Molecular Weight:471.50

IUPAC Name: (2S)-2-(((4aR,6S,7R,8R,8aS)-7-acetamido-6-(benzyloxy)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-8-yl)oxy)propanoic acid

InChIKey: JPPMVSNCFXDOJX-WAUMRMSNSA-N

SMILES: OC([C@H](C)O[C@H]1[C@@]2([H])[C@](COC(C3=CC=CC=C3)O2)([H])O[C@@H]([C@@H]1NC(C)=O)OCC4=CC=CC=C4)=O

Biological Activity: Benzyl N-acetyl-4,6-O-benzylidene-α-isomuramic acid 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-W703016
Benzyl N-acetyl-4,6-O-benzylidene-α-isomuramic acid Benzyl N-acetyl-4,6-O-benzylidene-α-isomuramic acid 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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