CC(=O)c1c(C)cc2cc(cc(O[C@@H]3O[C@H](CO)[C@]4(C[C@H]5[C@@H]6CC7(CCCC7)C[C@H]7COC[C@](CCO)([C@@H]67)C6=CCC(CO4)=C56)[C@H](O)[C@H]3O)c2c1O)C([O-])=O

InChIKey=MDNOWNTUPFWMFN-MYVFDYSTSA-M

C43H51O12

759.87

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Naphthalenecarboxylic acids Naphthols and derivatives Acetophenones Aryl alkyl ketones 1-hydroxy-4-unsubstituted benzenoids Oxanes Monosaccharides Vinylogous acids Secondary alcohols Acetals Oxacyclic compounds Carboxylic acids Dialkyl ethers Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Primary alcohols Organic anions

Aromatic heteropolycyclic compounds

Phenolic glycoside - 2-naphthalenecarboxylic acid - 2-naphthalenecarboxylic acid or derivatives - 1-naphthol - Naphthalene - Acetophenone - Aryl ketone - Aryl alkyl ketone - 1-hydroxy-4-unsubstituted benzenoid - Monosaccharide - Oxane - Benzenoid - 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