72647-96-2
Chemical Structure
4-Nitrophenyl 6-O-α-D-mannopyranosyl-α-D-mannopyranoside
- CAS No.: 72647-96-2
- Formula:C18H25NO13
- Molecular Weight:463.39
IUPAC Name: (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-(((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(4-nitrophenoxy)tetrahydro-2H-pyran-2-yl)methoxy)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: ISCYUJSLZREARS-LFVZYRDMSA-N
SMILES: OC[C@H]([C@H]([C@@H]([C@@H]1O)O)O)O[C@@H]1OC[C@H]([C@H]([C@@H]([C@@H]2O)O)O)O[C@@H]2OC3=CC=C(C=C3)[N+]([O-])=O
Biological Activity: 4-Nitrophenyl 6-O-α-D-mannopyranosyl-α-D-mannopyranoside 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 6-O-α-D-mannopyranosyl-α-D-mannopyranoside | 4-Nitrophenyl 6-O-α-D-mannopyranosyl-α-D-mannopyranoside 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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