16741-27-8
Chemical Structure
α-L-Galactopyranosyl bromide,6-deoxy,2,3,4-triacetate
Synonym(s): Acetobromofucose
- CAS No.: 16741-27-8
- Formula:C12H17BrO7
- Molecular Weight:353.16
IUPAC Name: (2S,3S,4R,5R,6S)-2-bromo-6-methyltetrahydro-2H-pyran-3,4,5-triyl triacetate
InChIKey: XUZQAPSYNYIKSR-BSOOIWJMSA-N
SMILES: CC(O[C@H]1[C@@H]([C@@H](O[C@H]([C@H]1OC(C)=O)C)Br)OC(C)=O)=O
Biological Activity: α-L-Galactopyranosyl bromide,6-deoxy,2,3,4-triacetate (Acetobromofucose) 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
α-L-Galactopyranosyl bromide,6-deoxy,2,3,4-triacetate | α-L-Galactopyranosyl bromide,6-deoxy,2,3,4-triacetate (Acetobromofucose) 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...
/
|
|||||||||||||||||||||||
