Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=PGWQTNMEWBOZOZ-YKPYJJBQSA-N

Formula

C20H19NO6

Mass

369.373

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 heteromonocyclic compounds

Substituents

Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Phenolic glycoside - Benzophenone - Diphenylmethane - Aryl-phenylketone - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Benzoyl - Phenoxy compound - Aryl ketone - Phenol ether - Benzonitrile - Monocyclic benzene moiety - Monosaccharide - Fatty acyl - Benzenoid - Oxane - Secondary alcohol - Ketone - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Nitrile - Carbonitrile - Hydrocarbon derivative - Organic oxide - Cyanide - Alcohol - Aldehyde - Organic nitrogen compound - Organonitrogen compound - Organopnictogen compound - Aromatic heteromonocyclic 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