23202-66-6
Chemical Structure
2,3,4,6-Tetra-O-acetyl-β-D-glucose
Synonym(s): Acetobromolaminaribiose
- CAS No.: 23202-66-6
- Formula:C26H35BrO17
- Molecular Weight:699.45
IUPAC Name: (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(((2R,3R,4S,5R,6R)-3,5-diacetoxy-2-(acetoxymethyl)-6-bromotetrahydro-2H-pyran-4-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
InChIKey: OCVWJMGXJXJBCO-VRECAULFSA-N
SMILES: CC(O[C@H]([C@H](O[C@@H]([C@@H]1OC(C)=O)Br)COC(C)=O)[C@@H]1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)COC(C)=O)OC(C)=O)OC(C)=O)OC(C)=O)=O
Biological Activity: 2,3,4,6-Tetra-O-acetyl-β-D-glucose (Acetobromolaminaribiose) 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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2,3,4,6-Tetra-O-acetyl-β-D-glucose | 2,3,4,6-Tetra-O-acetyl-β-D-glucose (Acetobromolaminaribiose) 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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Keywords