COC1=CC=CC2=C1C(=O)C1=C(C2O)C2=C(C=C(C)C=C2C=C1)[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O

InChIKey=CUDAFZMTMLPYBK-WOHLCTKUSA-N

C26H24O9

480.469

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Phenanthrols Anthracenes C-glucuronides C-glycosyl compounds Anisoles Aryl ketones Alkyl aryl ethers Beta hydroxy acids and derivatives Pyrans Oxanes Secondary alcohols Carboxylic acids Monocarboxylic acids and derivatives Oxacyclic compounds Polyols Dialkyl ethers Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenolic glycoside - Phenanthrol - Anthracene - C-glucuronide - Phenanthrene - Glucuronic acid or derivatives - C-glycosyl compound - Anisole - Aryl ketone - Phenol ether - Alkyl aryl ether - Beta-hydroxy acid - Benzenoid - Pyran - Hydroxy acid - Oxane - Secondary alcohol - Ketone - Ether - Dialkyl ether - Carboxylic acid - Carboxylic acid derivative - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Oxacycle - Polyol - Hydrocarbon derivative - Organic oxide - 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