CC(C)(O)C1CC2=C(O1)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)=C(CCC(O)=O)C=C2

InChIKey=PDUREEVYXLWDTJ-OOCDPMEESA-N

C20H28O10

428.434

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glycosyl compounds Coumarans Alkyl aryl ethers Benzenoids Monosaccharides Oxanes Tertiary alcohols Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Oxacyclic compounds Acetals Polyols Organic oxides Primary alcohols Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Phenolic glycoside - O-glycosyl compound - Coumaran - Alkyl aryl ether - Monosaccharide - Oxane - Benzenoid - Tertiary alcohol - Secondary alcohol - Polyol - Acetal - Monocarboxylic acid or derivatives - Ether - Carboxylic acid - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Primary alcohol - Alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxide - Aromatic heteropolycyclic 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