147103-31-9
Chemical Structure
4-Nitrophenyl 2-O-α-D-glucopyranosyl-α-D-glucopyranoside
- CAS No.: 147103-31-9
- Formula:C18H25NO13
- Molecular Weight:463.39
IUPAC Name: (2R,3R,4S,5S,6R)-2-(((2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-nitrophenoxy)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: ZGWCYKZKLZNQQX-TXSAWVTMSA-N
SMILES: OC[C@H]([C@H]([C@@H]([C@H]1O)O)O)O[C@@H]1O[C@H]([C@H]([C@@H]([C@H](O2)CO)O)O)[C@H]2OC3=CC=C(C=C3)[N+]([O-])=O
Biological Activity: 4-Nitrophenyl 2-O-α-D-glucopyranosyl-α-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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4-Nitrophenyl 2-O-α-D-glucopyranosyl-α-D-glucopyranoside | 4-Nitrophenyl 2-O-α-D-glucopyranosyl-α-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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