OC1C(COC(=O)\C=C\c2ccc(O)c(O)c2)OC(Oc2ccc(CCC(O)=O)cc2O)C(O)C1O

InChIKey=ZEAUIMYFGPAHKG-XBXARRHUSA-N

C24H26O12

506.46

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Cinnamic acid esters Coumaric acids and derivatives Phenylpropanoic acids O-glycosyl compounds Styrenes Phenoxy compounds Phenol ethers Catechols 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Fatty acid esters Oxanes Dicarboxylic acids and derivatives Monosaccharides Enoate esters Secondary alcohols Polyols Oxacyclic compounds Carboxylic acids Acetals Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Cinnamic acid or derivatives - Coumaric acid or derivatives - Hydroxycinnamic acid or derivatives - Cinnamic acid ester - O-glycosyl compound - 3-phenylpropanoic-acid - Phenoxy compound - Catechol - Phenol ether - Styrene - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Fatty acid ester - Phenol - Monocyclic benzene moiety - Fatty acyl - Oxane - Benzenoid - Monosaccharide - Dicarboxylic acid or derivatives - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Secondary alcohol - Carboxylic acid ester - Polyol - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Acetal - Carbonyl group - Hydrocarbon derivative - Alcohol - Organic oxide - Aromatic heteromonocyclic 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