CNC[C@@H](O)[C@]1(O)[C@H](O)C(O)(O)[C@H](OC2=CC=CC=C2)O[C@@H]1C(O)=O

InChIKey=BQSRWNRFUSHYFP-IGJDLRFWSA-N

C15H21NO9

359.331

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides Delta amino acids and derivatives O-glycosyl compounds Phenol ethers Phenoxy compounds Oxanes Pyrans Monosaccharides 1,3-aminoalcohols Tertiary alcohols 1,2-aminoalcohols Secondary alcohols Amino acids Oxacyclic compounds Polyols Monocarboxylic acids and derivatives Acetals Dialkylamines Carboxylic acids Carbonyl hydrates Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds

Aromatic heteromonocyclic compounds

Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Delta amino acid or derivatives - Glucuronic acid or derivatives - O-glycosyl compound - Phenoxy compound - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Oxane - Pyran - Benzenoid - Tertiary alcohol - 1,3-aminoalcohol - Amino acid - Secondary alcohol - Amino acid or derivatives - 1,2-aminoalcohol - Organoheterocyclic compound - Polyol - Oxacycle - Acetal - Secondary amine - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Carboxylic acid - Carboxylic acid derivative - Carbonyl hydrate - Alcohol - Carbonyl group - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Amine - 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