O[C@H]1[C@H](OC2=CC=CC3=C2N=CC=C3)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O

InChIKey=DPEGQJDYRIQRHI-DKBOKBLXSA-N

C15H15NO7

321.285

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides O-glycosyl compounds Quinolines and derivatives Beta hydroxy acids and derivatives Benzenoids Monosaccharides Pyridines and derivatives Pyrans Oxanes Heteroaromatic compounds Secondary alcohols Acetals Azacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Oxacyclic compounds Polyols Organic oxides Hydrocarbon derivatives Organonitrogen compounds Organopnictogen compounds Carbonyl compounds

Aromatic heteropolycyclic compounds

Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Quinoline - Beta-hydroxy acid - Hydroxy acid - Monosaccharide - Oxane - Pyran - Pyridine - Benzenoid - Heteroaromatic compound - Secondary alcohol - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Carboxylic acid - Acetal - Monocarboxylic acid or derivatives - Polyol - Carbonyl group - Organic nitrogen compound - Alcohol - Organic oxide - Hydrocarbon derivative - Organopnictogen compound - Organonitrogen compound - Aromatic heteropolycyclic 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