OC(=O)C1=CC(O)=C(O)C(O)=C1OC1=C(O)C(O)=C(C(=C1)C(O)=O)C1=C(O)C(O)=C(O)C=C1C(O)=O

InChIKey=RUOFGJLCWJUJRS-UHFFFAOYSA-N

C21H14O15

506.328

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Biphenols Diphenylethers Biphenyls and derivatives Gallic acids Diarylethers Pyrogallols and derivatives Benzoic acids Phenol ethers Phenoxy compounds Catechols Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Carboxylic acids Polyols Hydrocarbon derivatives Organic oxides

Aromatic homomonocyclic compounds

Hydrolyzable tannin - Biphenol - Diphenylether - Biphenyl - Gallic acid or derivatives - Gallic acid - Diaryl ether - Dihydroxybenzoic acid - Hydroxybenzoic acid - Benzoic acid or derivatives - Benzoic acid - Benzenetriol - Pyrogallol derivative - Benzoyl - Phenoxy compound - Catechol - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Benzenoid - Ether - Polyol - Carboxylic acid - Carboxylic acid derivative - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic 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) 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