O[C@H]1[C@H](OC2=CC=CC(C=CC(O)=O)=C2)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O

InChIKey=XPCHMFOWDFTFNV-DKBOKBLXSA-N

C15H16O9

340.284

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides Cinnamic acids Coumaric acids and derivatives Hexoses O-glycosyl compounds Phenol ethers Styrenes Phenoxy compounds Beta hydroxy acids and derivatives Oxanes Pyrans Dicarboxylic acids and derivatives Secondary alcohols Oxacyclic compounds Acetals Polyols Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteromonocyclic compounds

Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Cinnamic acid - Cinnamic acid or derivatives - Coumaric acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Styrene - Phenoxy compound - Phenol ether - Beta-hydroxy acid - Oxane - Pyran - Monosaccharide - Hydroxy acid - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Benzenoid - Secondary alcohol - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - Carboxylic acid - Carboxylic acid derivative - Hydrocarbon derivative - Carbonyl group - Alcohol - Organic oxide - 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