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

InChIKey=HPBSOAMJVDLGCG-XUYJXRERSA-N

C19H29NO8

399.44

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides O-glycosyl compounds Phenylpropanes Phenol ethers Phenoxy compounds Aralkylamines Beta hydroxy acids and derivatives Pyrans Oxanes Monosaccharides 1,3-aminoalcohols Tertiary alcohols Amino acids Secondary alcohols Polyols Acetals Oxacyclic compounds Carboxylic acids Dialkylamines Monocarboxylic acids and derivatives Carbonyl compounds Organopnictogen compounds Aromatic alcohols Hydrocarbon derivatives Organic oxides

Aromatic heteromonocyclic compounds

Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Phenylpropane - Phenoxy compound - Phenol ether - Beta-hydroxy acid - Aralkylamine - Oxane - Monocyclic benzene moiety - Pyran - Hydroxy acid - Monosaccharide - Benzenoid - 1,3-aminoalcohol - Tertiary alcohol - Secondary alcohol - Amino acid - Amino acid or derivatives - Acetal - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Secondary amine - Polyol - Organic nitrogen compound - Alcohol - Amine - Organopnictogen compound - Organic oxide - Aromatic alcohol - Hydrocarbon derivative - Carbonyl group - Organonitrogen 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