CC1OC(OCC2OC(OC3=CC4=C(OC3=C3C=CC(=O)C=C3)C=C(O)C=C4OC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O)C(O)C(O)C1[O+]=C(O)C=CC1=CC=C(O)C=C1

InChIKey=YRIQSIPLGNEDOM-UHFFFAOYSA-O

C42H47O21

887.816

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Cinnamic acids Coumaric acids Hydroxycinnamic acids Disaccharides O-glycosyl compounds 1-benzopyrans Styrenes P-quinomethanes 1-hydroxy-2-unsubstituted benzenoids Oxanes Secondary alcohols Monocarboxylic acids and derivatives Oxacyclic compounds Polyols Carboximidic acids Acetals Organic oxides Hydrocarbon derivatives Aldehydes Primary alcohols Organic cations

Aromatic heteropolycyclic compounds

Phenolic glycoside - Cinnamic acid - Cinnamic acid or derivatives - Coumaric acid - Coumaric acid or derivatives - Hydroxycinnamic acid - Hydroxycinnamic acid or derivatives - Disaccharide - O-glycosyl compound - 1-benzopyran - Benzopyran - Styrene - Quinomethane - P-quinomethane - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Oxane - Benzenoid - Secondary alcohol - Cyclic ketone - Ketone - Polyol - Carboximidic acid - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Acetal - Organoheterocyclic compound - Primary alcohol - Aldehyde - Organic oxide - Hydrocarbon derivative - Alcohol - Carbonyl group - Organic cation - 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