69948-03-4
Chemical Structure
p-Nitrophenyl β-D-cellobioside heptacetate
- CAS No.: 69948-03-4
- Formula:C32H39NO20
- Molecular Weight:757.65
IUPAC Name: (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(((2R,3R,4S,5R,6S)-4,5-diacetoxy-2-(acetoxymethyl)-6-(4-nitrophenoxy)tetrahydro-2H-pyran-3-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
InChIKey: NAPXHRWKTGFZTP-MMXCIQNPSA-N
SMILES: CC(O[C@H]([C@H]([C@@H](O[C@@H]1COC(C)=O)OC2=CC=C(C=C2)[N+]([O-])=O)OC(C)=O)[C@@H]1O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)COC(C)=O)OC(C)=O)OC(C)=O)OC(C)=O)=O
Biological Activity: p-Nitrophenyl β-D-cellobioside heptacetate 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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p-Nitrophenyl β-D-cellobioside heptacetate | p-Nitrophenyl β-D-cellobioside heptacetate 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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