OC1C(O)C2OC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)CC2OC1OC(=O)C1=CC(O)=C(O)C(O)=C1

InChIKey=DPRNKDPFIHTCKE-UHFFFAOYSA-N

C27H22O17

618.456

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Galloyl esters p-Hydroxybenzoic acid alkyl esters m-Hydroxybenzoic acid esters Pyrogallols and derivatives Aryl alkyl ketones Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Oxanes Dicarboxylic acids and derivatives Monosaccharides Secondary alcohols Carboxylic acid esters 1,2-diols Lactones Oxacyclic compounds Acetals Organic oxides Aldehydes Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Hydrolyzable tannin - Galloyl ester - Gallic acid or derivatives - P-hydroxybenzoic acid alkyl ester - M-hydroxybenzoic acid ester - P-hydroxybenzoic acid ester - Benzoate ester - Benzenetriol - Benzoic acid or derivatives - Pyrogallol derivative - Benzoyl - Aryl alkyl ketone - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Benzenoid - Monosaccharide - Oxane - Lactone - Ketone - Carboxylic acid ester - Secondary alcohol - 1,2-diol - Polyol - Organoheterocyclic compound - Acetal - Carboxylic acid derivative - Oxacycle - Alcohol - Organic oxygen compound - Organic oxide - Aldehyde - Organooxygen compound - Hydrocarbon derivative - 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