COC1=C(OC)C(OC)=C2C(=C1)[C@H](OC(C)=O)[C@H](C)[C@](C)(O)[C@@H](OC(=O)C1=CC=CC=C1)C1=CC(OC)=C(OC)C(OC)=C21

InChIKey=KXPCWLUANLWUAO-KGXBCIQTSA-N

C33H38O11

610.656

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Dibenzocyclooctadiene lignans Benzoic acid esters Benzoyl derivatives Anisoles Alkyl aryl ethers Dicarboxylic acids and derivatives Tertiary alcohols Carboxylic acid esters Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic homopolycyclic compounds

Hydrolyzable tannin - Dibenzocyclooctane lignan - Benzoate ester - Benzoic acid or derivatives - Anisole - Benzoyl - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Dicarboxylic acid or derivatives - Tertiary alcohol - Carboxylic acid ester - Ether - Carboxylic acid derivative - Carbonyl group - Alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic homopolycyclic compound

This compound belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Not available