C[C@H](CC(O)=O)C(=O)C1=C(O)C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=CC=C1

InChIKey=UCLRISWUPMTSAO-QJZHAOJPSA-N

C17H22O10

386.353

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Alkyl-phenylketones Hexoses Butyrophenones O-glycosyl compounds Phenylpropanes Aryl alkyl ketones Benzoyl derivatives Gamma-keto acids and derivatives Phenol ethers Phenoxy compounds 1-hydroxy-4-unsubstituted benzenoids Oxanes Vinylogous acids Secondary alcohols Polyols Monocarboxylic acids and derivatives Carboxylic acids Acetals Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Aldehydes Organic oxides

Aromatic heteromonocyclic compounds

Phenolic glycoside - Alkyl-phenylketone - Hexose monosaccharide - O-glycosyl compound - Butyrophenone - Phenylpropane - Phenylketone - Gamma-keto acid - Aryl alkyl ketone - Aryl ketone - Phenoxy compound - Benzoyl - Phenol ether - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Benzenoid - Keto acid - Monosaccharide - Oxane - Vinylogous acid - Ketone - Secondary alcohol - Monocarboxylic acid or derivatives - Acetal - Organoheterocyclic compound - Carboxylic acid - Carboxylic acid derivative - Oxacycle - Polyol - Primary alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aldehyde - 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