CO[C@H]1O[C@H](COC(=O)[C]2[CH][CH][CH][CH]2)[C@H](OC(=O)[C]2[CH][CH][CH][CH]2)[C@@H]2OC(=O)C3=CC(OC)=C(OC)C(OC)=C3C3=C(OC)C(OC)=C(OC)C=C3C(=O)O[C@@H]12

InChIKey=QZFDRGGFQBNBQR-MZLZATMCSA-N

C39H38O16

762.717

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Saccharolipids Tetracarboxylic acids and derivatives Gallic acid and derivatives Anisoles Alkyl aryl ethers Oxanes Monosaccharides Lactones Carboxylic acid esters Oxacyclic compounds Acetals Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Hydrolyzable tannin - Saccharolipid - Tetracarboxylic acid or derivatives - Gallic acid or derivatives - Anisole - Alkyl aryl ether - Benzenoid - Oxane - Monosaccharide - Carboxylic acid ester - Lactone - Acetal - Carboxylic acid derivative - Ether - Oxacycle - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organooxygen 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) 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