COC(=O)C1=CN(CC2=CC=CC=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=CC1=O

InChIKey=OKAZUPBBUYEVAZ-BFMVXSJESA-N

C20H23NO9

421.402

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Dihydropyridinecarboxylic acids and derivatives Pyridinecarboxylic acids Phenol ethers Phenoxy compounds Oxanes Methyl esters Heteroaromatic compounds Vinylogous amides Secondary alcohols Cyclic ketones Acetals Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Polyols Organopnictogen compounds Organonitrogen compounds Organic oxides Primary alcohols Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Dihydropyridinecarboxylic acid derivative - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Phenoxy compound - Phenol ether - Dihydropyridine - Monocyclic benzene moiety - Hydropyridine - Monosaccharide - Oxane - Pyridine - Benzenoid - Vinylogous amide - Methyl ester - Heteroaromatic compound - Carboxylic acid ester - Cyclic ketone - Secondary alcohol - Acetal - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Polyol - Organonitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Primary alcohol - 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