183875-28-7
Chemical Structure
Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside
- CAS No.: 183875-28-7
- Formula:C35H36O6S
- Molecular Weight:584.72
IUPAC Name: (2S,3R,4S,5S,6R)-4,5-bis(benzyloxy)-6-((benzyloxy)methyl)-2-(phenylthio)tetrahydro-2H-pyran-3-yl acetate
InChIKey: IKFDEPUTIUTSLC-NVCPMKERSA-N
SMILES: CC(O[C@H]1[C@H](SC2=CC=CC=C2)O[C@H](COCC3=CC=CC=C3)[C@H](OCC4=CC=CC=C4)[C@@H]1OCC5=CC=CC=C5)=O
Biological Activity: Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-bD-galactopyranoside 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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Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside | Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-bD-galactopyranoside 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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