[H][C@]1(CO)O[C@@]([H])(OC2=C(OC)C(OC)=C3C(CC[C@@]([H])(N=C(C)O)C4=CC(=O)C(OC)=CC=C34)=C2)[C@]([H])(O)[C@@]([H])(O)[C@]1([H])O

InChIKey=UXAFRQPVHYZDED-SUAFQAHMSA-N

C27H33NO11

547.557

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Tropones Anisoles Alkyl aryl ethers Oxanes Secondary alcohols Cyclic ketones Acetals Propargyl-type 1,3-dipolar organic compounds Carboximidic acids Polyols Oxacyclic compounds Primary alcohols Organopnictogen compounds Organic oxides Organonitrogen compounds

Aromatic heteropolycyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Anisole - Tropone - Alkyl aryl ether - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Cyclic ketone - Acetal - Carboximidic acid - Carboximidic acid derivative - Ether - Oxacycle - Organoheterocyclic compound - Polyol - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organonitrogen compound - Alcohol - Organic nitrogen compound - Primary alcohol - Organopnictogen compound - 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