4148-71-4
Chemical Structure
Methyl 2,3:4,6-di-O-benzylidene-α-D-mannopryanoside
- CAS. Nr.: 4148-71-4
- Formula:C21H22O6
- Molecular Weight:370.40
IUPAC Name: (3aS,4S,5aR,9aR,9bS)-4-methoxy-2,8-diphenylhexahydro-[1,3]dioxolo[4',5':4,5]pyrano[3,2-d][1,3]dioxine
InChIKey: VGLOFWHLPMVSBF-GGUYPNGTSA-N
SMILES: CO[C@@H]1[C@]2([H])[C@](OC(C3=CC=CC=C3)O2)([H])[C@@]4([H])[C@](COC(C5=CC=CC=C5)O4)([H])O1
Biological Activity: Methyl 2,3:4,6-di-O-benzylidene-α-D-mannopryanoside 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 2,3:4,6-di-O-benzylidene-α-D-mannopryanoside | Methyl 2,3:4,6-di-O-benzylidene-α-D-mannopryanoside 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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