CNC(C)CC1=CC=C(O[C@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(=O)OC)C=C1

InChIKey=VOXKXBMHGWGKPC-YWIVBLKHSA-N

C17H25NO7

355.387

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides O-glycosyl compounds Amphetamines and derivatives Phenylpropanes Phenoxy compounds Phenol ethers Aralkylamines Beta hydroxy acids and derivatives Pyrans Monosaccharides Oxanes Methyl esters Secondary alcohols Amino acids and derivatives Monocarboxylic acids and derivatives Dialkylamines Polyols Acetals Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organopnictogen compounds

Aromatic heteromonocyclic compounds

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