CCCCCC1=CC2=C(C3C=C(C)CCC3C(C)(C)O2)C(O)=C1C1OC(C(O)C(O)C1O)C(O)=O

InChIKey=PMPUBTMHJPJIII-UHFFFAOYSA-N

C27H38O8

490.593

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

C-glucuronides 2,2-dimethyl-1-benzopyrans C-glycosyl compounds Beta hydroxy acids and derivatives Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids Pyrans Oxanes Secondary alcohols Polyols Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Phenolic glycoside - C-glucuronide - Glucuronic acid or derivatives - 2,2-dimethyl-1-benzopyran - C-glycosyl compound - 1-benzopyran - Benzopyran - Chromane - 1-hydroxy-4-unsubstituted benzenoid - Beta-hydroxy acid - Alkyl aryl ether - Benzenoid - Pyran - Oxane - Hydroxy acid - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - Carboxylic acid derivative - Organic oxide - Hydrocarbon derivative - Carbonyl group - Alcohol - 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