CC(=O)[C@@H](O)[C@H]1O[C@@H](C2=CC(CC3=CC=C(O)C=C3)=C(C)C=C2)[C@@](O)(C(C)=O)[C@](O)(C(C)=O)[C@@]1(O)C(C)=O

InChIKey=GEGRQHGGGJIIOA-IIMJLWIBSA-N

C28H32O10

528.554

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Diphenylmethanes C-glycosyl compounds Aromatic monoterpenoids Iridoids and derivatives Monocyclic monoterpenoids Toluenes 1-hydroxy-2-unsubstituted benzenoids Acyloins Oxanes Alpha-hydroxy ketones Tertiary alcohols Secondary alcohols Oxacyclic compounds Dialkyl ethers Polyols Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Diphenylmethane - C-glycosyl compound - Secoiridoid-skeleton - Aromatic monoterpenoid - Monocyclic monoterpenoid - Monoterpenoid - 1-hydroxy-2-unsubstituted benzenoid - Toluene - Phenol - Acyloin - Monocyclic benzene moiety - Benzenoid - Oxane - Alpha-hydroxy ketone - Tertiary alcohol - Ketone - Secondary alcohol - Organoheterocyclic compound - Ether - Oxacycle - Dialkyl ether - Polyol - 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