Structure Information
Structure

Compound Identification

SMILES

[Na].COC1=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(OC)=C2C(CC[C@H](NC(C)=O)C3=CC(=O)C(SC)=CC=C23)=C1

InChIKey

InChIKey=KMZIXWDSCXVDHR-UNAHZUEVSA-N

Formula

C27H33NNaO10S

Mass

586.61

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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 - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Aryl thioether - Anisole - Tropone - Alkyl aryl ether - Alkylarylthioether - Oxane - Monosaccharide - Benzenoid - Fatty acyl - Acetamide - Secondary alcohol - Cyclic ketone - Secondary carboxylic acid amide - Carboxamide group - Acetal - Carboxylic acid derivative - Ether - Oxacycle - Organic alkali metal salt - Organoheterocyclic compound - Sulfenyl compound - Thioether - Polyol - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Organosulfur compound - Primary alcohol - Alcohol - 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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