CNC[C@H](O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)C1=CC(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=CC=C1

InChIKey=VDQQBBUYOKHAOY-GYSDEIIGSA-N

C21H29NO14

519.456

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides O-glycosyl compounds Phenoxy compounds Phenol ethers Aralkylamines Beta hydroxy acids and derivatives Pyrans Dicarboxylic acids and derivatives Monosaccharides Oxanes Secondary alcohols Amino acids Polyols Dialkylamines Carboxylic acids Acetals Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organopnictogen compounds

Aromatic heteromonocyclic compounds

Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Phenol ether - Phenoxy compound - Beta-hydroxy acid - Aralkylamine - Dicarboxylic acid or derivatives - Hydroxy acid - Benzenoid - Monosaccharide - Pyran - Oxane - Monocyclic benzene moiety - Amino acid - Amino acid or derivatives - Secondary alcohol - Acetal - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Oxacycle - Organoheterocyclic compound - Secondary amine - Polyol - Alcohol - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxide - Carbonyl group - Organonitrogen compound - 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