Structure Information
Structure

Compound Identification

SMILES

CC1(C)OC[C@H]2O[C@@H](OC3=CC=CC=C3CN)[C@H](O)[C@@H](O)[C@@H]2O1

InChIKey

InChIKey=JGJCHUQNNHFTQM-KJWHEZOQSA-N

Formula

C16H23NO6

Mass

325.361

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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 heteropolycyclic compounds

Substituents

Phenolic glycoside - Pyranodioxin - Benzylamine - Phenoxy compound - Phenol ether - Phenylmethylamine - Ketal - Aralkylamine - Meta-dioxane - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Oxane - Secondary alcohol - 1,2-diol - Oxacycle - Acetal - Organoheterocyclic compound - Primary amine - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Organic nitrogen compound - Amine - Alcohol - Organopnictogen compound - 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

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