CC(=O)[C@H]1O[C@@H](OC2=C(O)C=C(\C=C(\C)C(=O)N[C@H]3[C@@H](O)[C@@H]4OCO[C@@H]4[C@H](O)[C@@H]3O)C=C2)[C@@H](O)[C@@H]1O

InChIKey=YQYJSBFKSSDGFO-ATPAHKMZSA-N

C23H29NO12

511.48

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Cinnamic acid amides Hydroxycinnamic acids and derivatives O-glycosyl compounds Pentoses Phenoxy compounds Phenol ethers 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Cyclitols and derivatives 1,3-dioxolanes Tetrahydrofurans Ketones Secondary alcohols Secondary carboxylic acid amides Oxacyclic compounds Polyols Acetals Organonitrogen compounds Organic oxides Hydrocarbon derivatives Organopnictogen compounds

Aromatic heteropolycyclic compounds

Phenolic glycoside - Hydroxycinnamic acid or derivatives - Cinnamic acid amide - Cinnamic acid or derivatives - O-glycosyl compound - Pentose monosaccharide - Phenoxy compound - Phenol ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monosaccharide - Cyclitol or derivatives - Monocyclic benzene moiety - Benzenoid - Meta-dioxolane - Cyclic alcohol - Tetrahydrofuran - Ketone - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Acetal - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic nitrogen compound - Alcohol - Organopnictogen compound - Organonitrogen compound - 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