COC1=C(C)C2=C(C(=O)OC2)C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=C1CC=C(C)CCC(O)=O

InChIKey=BYFGTSAYQQIUCN-MOLMMISASA-N

C23H28O12

496.465

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides Hexoses O-glycosyl compounds Phthalides Tricarboxylic acids and derivatives Anisoles Beta hydroxy acids and derivatives Alkyl aryl ethers Oxanes Pyrans Secondary alcohols Lactones Carboxylic acid esters Acetals Oxacyclic compounds Carboxylic acids Polyols Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Isobenzofuranone - Phthalide - Isocoumaran - Tricarboxylic acid or derivatives - Anisole - Beta-hydroxy acid - Alkyl aryl ether - Pyran - Benzenoid - Oxane - Monosaccharide - Hydroxy acid - Carboxylic acid ester - Secondary alcohol - Lactone - Acetal - Ether - Carboxylic acid - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Polyol - Alcohol - Carbonyl group - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic 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