CC1=CC(O)=C(OC2=C(C)C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2C2=CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=CC(C)=C2O)C=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChIKey=GHOYAXMBMOQTOR-IDPOTYSHSA-N

C39H50O21

854.808

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Diphenylethers Biphenyls and derivatives Diarylethers O-glycosyl compounds 4-alkoxyphenols Phenoxy compounds Phenol ethers Ortho cresols Meta cresols 1-hydroxy-2-unsubstituted benzenoids Toluenes Oxanes Monosaccharides Secondary alcohols Oxacyclic compounds Acetals Polyols Hydrocarbon derivatives Primary alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - Diphenylether - Biphenyl - O-glycosyl compound - Diaryl ether - 4-alkoxyphenol - Phenoxy compound - O-cresol - Phenol ether - M-cresol - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Toluene - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Oxane - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Ether - Polyol - Hydrocarbon derivative - Primary alcohol - 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