CNC1=CC=C(C=C1)N=NC1=CC=C(C=C1)C1(O)O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O

InChIKey=UMMQSUFZSDIBIV-VPQNOXPISA-N

C19H21N3O7

403.391

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Azobenzenes C-glucuronides Aniline and substituted anilines Phenylalkylamines Secondary alkylarylamines Beta hydroxy acids and derivatives Pyrans Oxanes Monosaccharides Azo compounds Amino acids Secondary alcohols Hemiacetals Carboxylic acids Polyols Oxacyclic compounds Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Carbonyl compounds Hydrocarbon derivatives Organic oxides

Aromatic heteromonocyclic compounds

Phenolic glycoside - Azobenzene - C-glucuronide - Glucuronic acid or derivatives - Aniline or substituted anilines - Phenylalkylamine - Secondary aliphatic/aromatic amine - Beta-hydroxy acid - Benzenoid - Hydroxy acid - Oxane - Pyran - Monocyclic benzene moiety - Monosaccharide - Amino acid - Azo compound - Hemiacetal - Amino acid or derivatives - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Secondary amine - Monocarboxylic acid or derivatives - Polyol - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Amine - Carbonyl group - 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