OS(=O)(=O)OC1=C(OS(O)(=O)=O)C2=C3C(=C1)C(=O)OC1=C3C(=CC(OS(O)(=O)=O)=C1OS(O)(=O)=O)C(=O)O2

InChIKey=FCDRKJVABFYWBJ-UHFFFAOYSA-N

C14H6O20S4

622.42

Organic compounds

Phenylpropanoids and polyketides

Tannins

Hydrolyzable tannins

Not available

Hydrolyzable tannins

Ellagic acids and derivatives Isocoumarins and derivatives Coumarins and derivatives Arylsulfates 2-benzopyrans 1-benzopyrans Pyranones and derivatives Sulfuric acid monoesters Heteroaromatic compounds Lactones Oxacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Hydrolyzable tannin - Ellagic_acid - Coumarin - Isocoumarin - Benzopyran - Arylsulfate - 2-benzopyran - 1-benzopyran - Pyranone - Benzenoid - Sulfuric acid ester - Sulfate-ester - Sulfuric acid monoester - Pyran - Heteroaromatic compound - Organic sulfuric acid or derivatives - Lactone - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - 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) 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