CC(C)(O)\C=C\C1=CC(=CC(\C=C\C(C)(C)O)=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)OC[C@H]1O[C@H](O[C@]2(CO)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey=IVPYFUBJLVMEBF-FGPUJWTJSA-N

C35H52O20

792.781

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

C-glycosyl compounds Disaccharides O-glycosyl compounds Benzoic acid esters Cinnamyl alcohols Benzoyl derivatives Styrenes Phenol ethers Phenoxy compounds Ketals Oxanes Oxolanes Tertiary alcohols Secondary alcohols Carboxylic acid esters Oxacyclic compounds Polyols Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Primary alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - C-glycosyl compound - Disaccharide - O-glycosyl compound - Benzoate ester - Cinnamyl alcohol - Benzoic acid or derivatives - Phenoxy compound - Benzoyl - Styrene - Phenol ether - Ketal - Monocyclic benzene moiety - Benzenoid - Oxane - Tertiary alcohol - Oxolane - Secondary alcohol - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Alcohol - Hydrocarbon derivative - Organic oxide - 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