Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H](OC2=CC3=C(C[C@@H](C([O-])=O)[N+]3=CC=C3C[C@H](NC(=C3)C([O-])=O)C([O-])=O)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=YUDKHXMQDKVDGU-KOLAXLCUSA-L

Formula

C24H24N2O13

Mass

548.458

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Glycosyl compounds

Direct Parent

Phenolic glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phenolic glycoside - Betalamic acid or derivatives - Indolecarboxylic acid derivative - Indolecarboxylic acid - Hexose monosaccharide - O-glycosyl compound - L-alpha-amino acid - Alpha-amino acid or derivatives - Alpha-amino acid - Alkaloid or derivatives - Tricarboxylic acid or derivatives - Indole or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Tetrahydropyridine - Benzenoid - Oxane - Monosaccharide - Hydropyridine - Amino acid - Shiff base - Secondary alcohol - Carboxylic acid salt - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Polyol - Enamine - Secondary aliphatic amine - Carboxylic acid - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Primary alcohol - Organonitrogen compound - Carbonyl group - Amine - Alcohol - Organic anion - Aromatic heteropolycyclic compound

Description

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.

External Descriptors

Not available

Previous Back Next