C[C@@]1(O)[C@@H](O)[C@@H](O)[C@@H](CO)O[C@]1(O)C1=CC(=C(C(=C1)[N+]([O-])=O)[C@@]1(O)O[C@H](CO)[C@H](O)[C@H](O)[C@@]1(C)O)[C@@]1(O)O[C@H](CO)[C@H](O)[C@H](O)[C@@]1(C)O

InChIKey=WGUVGALZSYBREB-JIRVUWICSA-N

C27H41NO20

699.612

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Nitrobenzenes Nitroaromatic compounds Monosaccharides Oxanes Tertiary alcohols Hemiacetals Secondary alcohols 1,2-diols Oxacyclic compounds Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Organonitrogen compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives Primary alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - Nitrobenzene - Nitroaromatic compound - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Tertiary alcohol - Organic nitro compound - Hemiacetal - 1,2-diol - Secondary alcohol - C-nitro compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Polyol - Oxacycle - Organic oxoazanium - Organic salt - Organonitrogen compound - Hydrocarbon derivative - Primary alcohol - Organic oxide - Organic zwitterion - Organic nitrogen compound - Alcohol - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Not available