13992-16-0
Chemical Structure
Phenyl 2,3,4,6-tetra-O-acetyl-α-D-thiomannopyranoside
- CAS No.: 13992-16-0
- Formula:C20H24O9S
- Molecular Weight:440.46
IUPAC Name: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate
InChIKey: JCKOUAWEMPKIAT-OUUBHVDSSA-N
SMILES: CC(O[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)=O
Biological Activity: Phenyl 2,3,4,6-tetra-O-acetyl-α-D-thiomannopyranoside 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].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Phenyl 2,3,4,6-tetra-O-acetyl-α-D-thiomannopyranoside | Phenyl 2,3,4,6-tetra-O-acetyl-α-D-thiomannopyranoside 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. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||