CC(N)=C1C(=O)C=C2OC3=C(C(C)=O)C(OC4OC(CO)C(O)C(O)C4O)=C(C)C(O)=C3C2(C)C1=O

InChIKey=CIARKHUADCATCL-UHFFFAOYSA-N

C24H27NO11

505.476

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Fatty acyl glycosides of mono- and disaccharides Alkyl glycosides Hexoses O-glycosyl compounds Acetophenones Coumarans Aryl alkyl ketones O-quinomethanes Cyclohexenones Oxanes Vinylogous esters Vinylogous amides Secondary alcohols Acetals Polyols Oxacyclic compounds Enamines Organopnictogen compounds Aldehydes Organic oxides Primary alcohols Monoalkylamines Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Fatty acyl glycoside - Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Acetophenone - Coumaran - Quinomethane - Aryl ketone - Aryl alkyl ketone - O-quinomethane - Cyclohexenone - Benzenoid - Monosaccharide - Oxane - Fatty acyl - Vinylogous ester - Vinylogous amide - Ketone - Cyclic ketone - Secondary alcohol - Acetal - Enamine - Oxacycle - Organoheterocyclic compound - Polyol - Aldehyde - Alcohol - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Amine - Primary aliphatic amine - Primary amine - Primary 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