20689-03-6
Chemical Structure
Phenylmethyl 2,3-O-(1-methylethylidene)-α-D-mannofuranoside
- CAS No.: 20689-03-6
- Formula:C16H22O6
- Molecular Weight:310.34
IUPAC Name: (R)-1-((3aS,4R,6S,6aS)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)ethane-1,2-diol
InChIKey: NKCNUNUEQRYLNZ-MRLBHPIUSA-N
SMILES: OC[C@H]([C@]1([H])[C@@]2([H])[C@@](OC(C)(O2)C)([H])[C@H](O1)OCC3=CC=CC=C3)O
Biological Activity: Phenylmethyl 2,3-O-(1-methylethylidene)-α-D-mannofuranoside 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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Phenylmethyl 2,3-O-(1-methylethylidene)-α-D-mannofuranoside | Phenylmethyl 2,3-O-(1-methylethylidene)-α-D-mannofuranoside 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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