82628-87-3
Chemical Structure
4′-O-(β-D-2″,3″,4″,6″-Tetraacetyl-glucopyranosyl)-4-nitrophloretin
- CAS No.: 82628-87-3
- Formula:C29H31NO15
- Molecular Weight:633.55
IUPAC Name: (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(3,5-dihydroxy-4-(3-(4-nitrophenyl)propanoyl)phenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
InChIKey: SGHSVHIGFLBYAX-KRZJEZTLSA-N
SMILES: CC(O[C@@H]1[C@H]([C@@H](O[C@@H]([C@H]1OC(C)=O)COC(C)=O)OC2=CC(O)=C(C(O)=C2)C(CCC3=CC=C(C=C3)[N+]([O-])=O)=O)OC(C)=O)=O
Biological Activity: 4′-O-(β-D-2″,3″,4″,6″-Tetraacetyl-glucopyranosyl)-4-nitrophloretin 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′-O-(β-D-2″,3″,4″,6″-Tetraacetyl-glucopyranosyl)-4-nitrophloretin | 4′-O-(β-D-2″,3″,4″,6″-Tetraacetyl-glucopyranosyl)-4-nitrophloretin 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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