CC(=O)\C=C\C=C\C1=CC(O)=C(O[C@@H]2OC(CO)[C@H](O)[C@H](O)C2O)C=C1

InChIKey=BOJJATMVYSVQPJ-QAQLUZMWSA-N

C18H22O8

366.366

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Fatty acyl glycosides of mono- and disaccharides Alkyl glycosides Hexoses O-glycosyl compounds Styrenes Phenol ethers Phenoxy compounds 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Oxanes Enones Acryloyl compounds Ketones Secondary alcohols Oxacyclic compounds Polyols Acetals Organic oxides Hydrocarbon derivatives Primary alcohols Aldehydes

Aromatic heteromonocyclic compounds

Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Phenolic glycoside - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Phenol ether - Styrene - Phenoxy compound - Phenol - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Oxane - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Monosaccharide - Acryloyl-group - Enone - Alpha,beta-unsaturated ketone - Ketone - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aldehyde - Primary alcohol - 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