OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)C1=C(O)C=C(O)C(C(=O)C2=CC=C(O)C=C2)=C1O

InChIKey=BZYKNVLTMWYEFA-ZJKJAXBQSA-N

C19H20O10

408.359

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Benzophenones Aryl-phenylketones Diphenylmethanes C-glycosyl compounds Phloroglucinols and derivatives Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Monosaccharides Oxanes Vinylogous acids Secondary alcohols Oxacyclic compounds Polyols Dialkyl ethers Organic oxides Hydrocarbon derivatives Primary alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - Benzophenone - Diphenylmethane - Aryl-phenylketone - C-glycosyl compound - Phloroglucinol derivative - Benzenetriol - Benzoyl - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Benzenoid - Oxane - Monocyclic benzene moiety - Monosaccharide - Vinylogous acid - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Dialkyl ether - Polyol - Ether - Primary alcohol - Organic oxide - Hydrocarbon derivative - Alcohol - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Not available