CC(=O)OCC1OC(Oc2c(C)c(O)c3c(oc(C)cc3=O)c2C)C(OC(C)=O)C(O)C1O

InChIKey=JJJSQCWFEPGDOF-UHFFFAOYSA-N

C22H26O11

466.439

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glycosyl compounds Chromones Pyranones and derivatives Oxanes Benzenoids Monosaccharides Dicarboxylic acids and derivatives Vinylogous acids Heteroaromatic compounds Secondary alcohols 1,2-diols Carboxylic acid esters Oxacyclic compounds Acetals Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenolic glycoside - Chromone - O-glycosyl compound - Benzopyran - 1-benzopyran - Pyranone - Dicarboxylic acid or derivatives - Monosaccharide - Oxane - Benzenoid - Pyran - Heteroaromatic compound - Vinylogous acid - 1,2-diol - Carboxylic acid ester - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Acetal - Hydrocarbon derivative - Carbonyl group - Organic oxide - 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