Structure Information
Structure

Compound Identification

SMILES

OCC1OC(OC2=CC(O)=C(C=C2)C(=O)CC2=CC=CC=N2)C(O)C(O)C1O

InChIKey

InChIKey=CUMKQHYXWAXCIZ-UHFFFAOYSA-N

Formula

C19H21NO8

Mass

391.376

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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 - Alkyl-phenylketone - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Phenylketone - Phenol ether - Phenoxy compound - Aryl ketone - Aryl alkyl ketone - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Fatty acyl - Monosaccharide - Pyridine - Oxane - Benzenoid - Monocyclic benzene moiety - Vinylogous acid - Heteroaromatic compound - Ketone - Secondary alcohol - Organoheterocyclic compound - Acetal - Azacycle - Oxacycle - Polyol - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Aldehyde - Primary alcohol - 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

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