210297-54-4
Chemical Structure
Methyl 2-O-allyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside
- CAS No.: 210297-54-4
- Formula:C24H28O6
- Molecular Weight:412.48
IUPAC Name: (4aR,6S,7S,8S,8aR)-7-(allyloxy)-8-(benzyloxy)-6-methoxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxine
InChIKey: YFGKDDPSSKUWEG-NBOVQHNFSA-N
SMILES: CO[C@H]([C@H]1OCC=C)O[C@@](COC(C2=CC=CC=C2)O3)([H])[C@]3([H])[C@@H]1OCC4=CC=CC=C4
Biological Activity: Methyl 2-O-allyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 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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Methyl 2-O-allyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside | Methyl 2-O-allyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 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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