CCCN(CCC)C1CCC2=C(C1)C(O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)=CC=C2

InChIKey=QUOYRPQHPXIBEH-PLEVBHNASA-N

C22H33NO7

423.506

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides Hexoses O-glycosyl compounds Tetralins Aralkylamines Beta hydroxy acids and derivatives Pyrans Oxanes Trialkylamines Secondary alcohols Amino acids Acetals Polyols Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Tetralin - Beta-hydroxy acid - Aralkylamine - Oxane - Hydroxy acid - Pyran - Monosaccharide - Benzenoid - Secondary alcohol - Tertiary amine - Amino acid - Tertiary aliphatic amine - Amino acid or derivatives - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Polyol - Amine - Alcohol - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organopnictogen compound - Carbonyl group - 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