878495-64-8
Chemical Structure
5-Bromo-6-chloro-3-indolyl a-D-glucopyranoside
- CAS No.: 878495-64-8
- Formula:C14H15BrClNO6
- Molecular Weight:408.63
IUPAC Name: (2R,3R,4S,5S,6R)-2-((5-bromo-6-chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: CHRVKCMQIZYLNM-RGDJUOJXSA-N
SMILES: ClC(C=C1C(C(O[C@H]2O[C@@H]([C@H]([C@@H]([C@H]2O)O)O)CO)=CN1)=C3)=C3Br
Biological Activity: 5-Bromo-6-chloro-3-indolyl a-D-glucopyranoside 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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5-Bromo-6-chloro-3-indolyl a-D-glucopyranoside | 5-Bromo-6-chloro-3-indolyl a-D-glucopyranoside 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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