OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)C1=C(O)C=CC2=C1O[C@]13C[C@H](O[C@@](O)(C1)C(=O)C=C23)C(O)=O

InChIKey=KVCDMLSZBATQNF-RCMVGFPFSA-N

C21H22O12

466.395

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses C-glycosyl compounds Coumarans Cyclohexenones Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Pyrans Oxanes Secondary alcohols Hemiacetals Polyols Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenolic glycoside - Hexose monosaccharide - C-glycosyl compound - Coumaran - 1-hydroxy-2-unsubstituted benzenoid - Cyclohexenone - Alkyl aryl ether - Benzenoid - Pyran - Oxane - Monosaccharide - Secondary alcohol - Ketone - Hemiacetal - Oxacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - Carboxylic acid derivative - Organic oxide - Hydrocarbon derivative - Primary alcohol - 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