[K+].OC[C@H]1O[C@@H](OC2=CC=C(\C=C/C([O-])=O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey=RIRDDCAJGBKKGD-JMOWHWDFSA-M

C15H17KO8

364.391

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Cinnamic acids Hexoses O-glycosyl compounds Styrenes Phenol ethers Phenoxy compounds Oxanes Secondary alcohols Carboxylic acid salts Oxacyclic compounds Monocarboxylic acids and derivatives Acetals Carboxylic acids Polyols Organic zwitterions Organic potassium salts Organic oxides Primary alcohols Hydrocarbon derivatives Carbonyl compounds

Aromatic heteromonocyclic compounds

Phenolic glycoside - Cinnamic acid - Cinnamic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Phenoxy compound - Styrene - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Oxane - Carboxylic acid salt - Secondary alcohol - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Organic alkali metal salt - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Polyol - Organic oxide - Carbonyl group - Organic potassium salt - Alcohol - Hydrocarbon derivative - Organic salt - Organic zwitterion - Primary 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