OC[C@H]1O[C@@H](Oc2ccc(C=CC(O)=O)cc2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey=LJFYQZQUAULRDF-TVKJYDDYSA-N

C15H18O8

326.301

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Cinnamic acids Hexoses O-glycosyl compounds Styrenes Phenol ethers Phenoxy compounds Oxanes Secondary alcohols Oxacyclic compounds Monocarboxylic acids and derivatives Acetals Carboxylic acids Polyols Organic oxides Primary alcohols Hydrocarbon derivatives Carbonyl compounds

Aromatic heteromonocyclic compounds

Phenolic glycoside - Cinnamic acid - Cinnamic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Phenoxy compound - Phenol ether - Styrene - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid - Carboxylic acid derivative - Acetal - Polyol - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Primary 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.

CHEBI:17335 : olefinic phospholipid - glucosyl hydroxycinnamic acid