COC(=O)C1=CC(OC)=C2OCOC2=C1C1=C2OCOC2=C(OC)C=C1C=CC(=O)C1=CC=C(O)C=C1

InChIKey=KSCZJZOUMDVFON-UHFFFAOYSA-N

C27H22O10

506.463

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Retrochalcones Gallic acid and derivatives Cinnamic acids and derivatives M-methoxybenzoic acids and derivatives Benzodioxoles Styrenes Anisoles Aryl ketones Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Acryloyl compounds Methyl esters Enones Monocarboxylic acids and derivatives Acetals Oxacyclic compounds Organic oxides Aldehydes Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Hydrolyzable tannin - Retrochalcone - Cinnamic acid or derivatives - Gallic acid or derivatives - M-methoxybenzoic acid or derivatives - Benzodioxole - Anisole - Benzoyl - Aryl ketone - Styrene - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Monocyclic benzene moiety - Benzenoid - Methyl ester - Acryloyl-group - Alpha,beta-unsaturated ketone - Enone - Ketone - Carboxylic acid ester - Monocarboxylic acid or derivatives - Acetal - Oxacycle - Carboxylic acid derivative - Ether - Organoheterocyclic compound - Organooxygen compound - Hydrocarbon derivative - Aldehyde - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic 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