COC(=O)[C@@H]1OC(=O)C2=CC(OC)=C(OC)C(OC)=C2C2=C3C(=C(OC)C(OC)=C2OC)C2=C(OC)C(OC)=C(OC)C=C2C(=O)O[C@@H]2COC(=O)C4=CC(OC)=C(OC)C(OC)=C4C4=C(OC)C(OC)=C(OC)C=C4C(=O)O[C@H]2[C@@H]1OC3=O

InChIKey=GKMJVKVXRDQLLG-ZPONUINGSA-N

C57H58O27

1175.064

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Gallic acid and derivatives Anisoles Alkyl aryl ethers Methyl esters Lactones Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Hydrolyzable tannin - Gallic acid or derivatives - Anisole - Phenol ether - Alkyl aryl ether - Benzenoid - Methyl ester - Carboxylic acid ester - Lactone - Carboxylic acid derivative - Ether - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organooxygen compound - Organic oxygen compound - 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) 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