CCOC1=C([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C2=C(C(C)=C1)C(=O)C=C(CC(C)=O)O2

InChIKey=JPKGIZQYWQECEF-VPRICQMDSA-N

C21H26O9

422.43

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses C-glycosyl compounds Chromones Phenol ethers Alkyl aryl ethers Pyranones and derivatives Oxanes Heteroaromatic compounds 1,2-diols Secondary alcohols Ketones Dialkyl ethers Oxacyclic compounds Organic oxides Primary alcohols Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenolic glycoside - Hexose monosaccharide - C-glycosyl compound - Chromone - Benzopyran - 1-benzopyran - Phenol ether - Pyranone - Alkyl aryl ether - Benzenoid - Pyran - Oxane - Monosaccharide - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Ketone - Organoheterocyclic compound - Polyol - Dialkyl ether - Ether - Oxacycle - Hydrocarbon derivative - Carbonyl group - Alcohol - Primary alcohol - 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