1820572-28-8
Chemical Structure
Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-β-D-thiogalactopyranoside
Synonym(s): Gal[246Ac,3All]-β-SPh
- CAS No.: 1820572-28-8
- Formula:C21H26O8S
- Molecular Weight:438.49
IUPAC Name: (2R,3S,4S,5R,6S)-2-(acetoxymethyl)-4-(allyloxy)-6-(phenylthio)tetrahydro-2H-pyran-3,5-diyl diacetate
InChIKey: AEZBNOXQHIZNTR-IFLJBQAJSA-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-β-d-Thiogalactopyranoside (Gal[246Ac,3All]-β-SPh) is a class of biochemical reagents used for glycobiology research. 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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Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-β-D-thiogalactopyranoside | Phenyl 2,4, 6-tri-o-acetyl-3-o-allyl-β-d-Thiogalactopyranoside (Gal[246Ac,3All]-β-SPh) is a class of biochemical reagents used for glycobiology research. 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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