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-KEHBMHOOSA-N

C23H29NO12

511.48

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

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

Aromatic heteropolycyclic compounds

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