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

InChIKey=QBFLNEGRIWWRPZ-GOVZDWNOSA-N

C12H14O8

286.236

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides O-glycosyl compounds Phenoxy compounds Phenol ethers 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Beta hydroxy acids and derivatives Pyrans Monosaccharides Oxanes Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Polyols Acetals Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteromonocyclic compounds

Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Phenoxy compound - Phenol ether - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Beta-hydroxy acid - Hydroxy acid - Benzenoid - Pyran - Monosaccharide - Oxane - Monocyclic benzene moiety - Secondary alcohol - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Organic oxide - Hydrocarbon derivative - Carbonyl group - 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