O[C@@H]1[C@@H](O)[C@H](OC2=CC=C(\C=C\C([O-])=O)C=C2)O[C@@H]([C@H]1O)C([O-])=O

InChIKey=SOKJXEKPKWKYKR-KPGYTNHDSA-L

C15H14O9

338.269

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides Cinnamic acids Hexoses O-glycosyl compounds Phenoxy compounds Phenol ethers Styrenes Beta hydroxy acids and derivatives Oxanes Pyrans Dicarboxylic acids and derivatives Carboxylic acid salts Secondary alcohols Oxacyclic compounds Polyols Acetals Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic anions

Aromatic heteromonocyclic compounds

Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Cinnamic acid - Cinnamic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Phenoxy compound - Phenol ether - Styrene - Beta-hydroxy acid - Pyran - Oxane - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Hydroxy acid - Dicarboxylic acid or derivatives - Secondary alcohol - Carboxylic acid salt - Polyol - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Carboxylic acid - Acetal - Alcohol - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organic anion - 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