C[C@H]1[C@@H]2C[C@]3(OCC4=C2C(=CC4)[C@]2(CCCO)COCC[C@@H]12)[C@H](O)[C@@H](O)[C@H](Oc1cc(cc2c(O)c(C)c(C(C)=O)c(O)c12)C([O-])=O)O[C@@H]3CO

InChIKey=FJGRQCTWIAEQCR-KOQTUPLWSA-M

C38H45O13

709.766

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Naphthalenecarboxylic acids Naphthols and derivatives Acetophenones Aryl alkyl ketones Hydroquinones Oxanes Monosaccharides Vinylogous acids Secondary alcohols Acetals Oxacyclic compounds Carboxylic acids Dialkyl ethers Monocarboxylic acids and derivatives Hydrocarbon derivatives Organic oxides Primary alcohols Organic anions

Aromatic heteropolycyclic compounds

Phenolic glycoside - 2-naphthalenecarboxylic acid - 2-naphthalenecarboxylic acid or derivatives - 1-naphthol - Naphthalene - Acetophenone - Hydroquinone - Aryl ketone - Aryl alkyl ketone - Benzenoid - Oxane - Monosaccharide - Vinylogous acid - Secondary alcohol - Ketone - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Acetal - Monocarboxylic acid or derivatives - Oxacycle - Organoheterocyclic compound - Alcohol - Primary alcohol - Organic oxide - Hydrocarbon derivative - Organic anion - 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