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

InChIKey=JRFMKQUGXNLLIH-GLEXUSGWSA-N

C15H23NO8

345.348

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Phenol ethers Phenoxy compounds Aralkylamines 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Oxanes 1,2-aminoalcohols Secondary alcohols Oxacyclic compounds Dialkylamines Acetals Polyols Organopnictogen compounds Primary alcohols Hydrocarbon derivatives Aromatic alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Phenoxy compound - Phenol ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Phenol - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Oxane - 1,2-aminoalcohol - Secondary alcohol - Acetal - Secondary aliphatic amine - Oxacycle - Organoheterocyclic compound - Secondary amine - Polyol - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Amine - Organonitrogen compound - Aromatic alcohol - Primary alcohol - Organopnictogen compound - 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