CC1=NC2=C(C=C(O[C@@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C([O-])=O)C=C2)C(=O)N1C1=CC=CC=C1C

InChIKey=WKXWFAVXGQVYFU-KSSXRGRSSA-M

C22H21N2O8

441.417

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides O-glycosyl compounds Quinazolines Toluenes Beta hydroxy acids and derivatives Pyrimidones Monosaccharides Pyrans Oxanes Heteroaromatic compounds Lactams Carboxylic acid salts Secondary alcohols Polyols Azacyclic compounds Acetals Monocarboxylic acids and derivatives Carboxylic acids Oxacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organopnictogen compounds Organic anions

Aromatic heteropolycyclic compounds

Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Diazanaphthalene - Quinazoline - Beta-hydroxy acid - Pyrimidone - Toluene - Benzenoid - Monocyclic benzene moiety - Oxane - Pyrimidine - Pyran - Monosaccharide - Hydroxy acid - Heteroaromatic compound - Secondary alcohol - Carboxylic acid salt - Lactam - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Organic nitrogen compound - Organopnictogen compound - Carbonyl group - Alcohol - Organic oxide - Organonitrogen compound - Organic anion - 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