[H].CC(=O)C1=C2C[C@H](OC(=O)C2=C(OC2OC(CO)C(O)C(O)C2O)C=C1O)\C=C\C=C\C=O

InChIKey=NWHAAFAGKFHVPJ-NIWUMKGASA-N

C22H25O11

465.431

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds 2-benzopyrans Acetophenones Aryl alkyl ketones 1-hydroxy-2-unsubstituted benzenoids Oxanes Vinylogous acids Enals Lactones Carboxylic acid esters Secondary alcohols Oxacyclic compounds Monocarboxylic acids and derivatives Polyols Acetals Hydrocarbon derivatives Aldehydes Primary alcohols Organic oxides

Aromatic heteropolycyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Benzopyran - Isochromane - 2-benzopyran - Acetophenone - Aryl alkyl ketone - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - Monosaccharide - Oxane - Benzenoid - Alpha,beta-unsaturated aldehyde - Vinylogous acid - Enal - Secondary alcohol - Carboxylic acid ester - Lactone - Ketone - Polyol - Oxacycle - Carboxylic acid derivative - Acetal - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Hydrocarbon derivative - Alcohol - Carbonyl group - Primary alcohol - Aldehyde - 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