197005-22-4
Chemical Structure
Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-glucopyranoside
- CAS No.: 197005-22-4
- Formula:C21H26O8S
- Molecular Weight:438.49
IUPAC Name: (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-4-(allyloxy)-6-(phenylthio)tetrahydro-2H-pyran-3,5-diyl diacetate
InChIKey: AEZBNOXQHIZNTR-ADAARDCZSA-N
SMILES: C=CCO[C@@H]1[C@H]([C@@H](O[C@@H]([C@H]1OC(C)=O)COC(C)=O)SC2=CC=CC=C2)OC(C)=O
Biological Activity: Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-glucopyranoside 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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Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-glucopyranoside | Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-glucopyranoside 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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