141020-28-2
Chemical Structure
Benzyl 2-acetamido-2,6-dideoxy-3-O-β-D-galactopyranosyl α-D-galactopyranoside
- CAS No.: 141020-28-2
- Formula:C21H31NO10
- Molecular Weight:457.47
IUPAC Name: N-((2S,3R,4R,5S,6R)-2-(benzyloxy)-5-hydroxy-6-methyl-4-(((2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-3-yl)acetamide
InChIKey: HGURJGMYXKMOOM-QAYXKSKNSA-N
SMILES: C[C@@H]1[C@H](O)[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O2)[C@@H](NC(C)=O)[C@@H](OCC3=CC=CC=C3)O1
Biological Activity: Benzyl 2-acetamido-2, 6-dideoxy-3-o-β-D-Galactopyranosyl-α-d-Galactopyranoside is a class of biochemical reagents used in glycobiology studies. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It deals with carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. The field is closely related to basic research, biomedicine and biotechnology[1].
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Benzyl 2-acetamido-2,6-dideoxy-3-O-β-D-galactopyranosyl α-D-galactopyranoside | Benzyl 2-acetamido-2, 6-dideoxy-3-o-β-D-Galactopyranosyl-α-d-Galactopyranoside is a class of biochemical reagents used in glycobiology studies. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It deals with carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. The field is closely related to basic research, biomedicine and biotechnology. | |||||||||||||||||||||
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