Structure Information
Structure

Compound Identification

SMILES

OC1C(O)C(COC(=O)C2=CC(O)=C(O)C(O)=C2)OC(OC2=C(O)C=C(C=C2O)C(O)=O)C1O

InChIKey

InChIKey=YWUUUONTCOYVTR-UHFFFAOYSA-N

Formula

C20H20O14

Mass

484.366

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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

Phenolic glycoside - Galloyl ester - Gallic acid or derivatives - O-glycosyl compound - P-hydroxybenzoic acid alkyl ester - M-hydroxybenzoic acid ester - P-hydroxybenzoic acid ester - Hydroxybenzoic acid - Benzoate ester - Benzoic acid - Pyrogallol derivative - Benzenetriol - Benzoic acid or derivatives - Phenoxy compound - Phenol ether - Resorcinol - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Phenol - 1-hydroxy-4-unsubstituted benzenoid - Sugar acid - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Oxane - Monosaccharide - Benzenoid - Carboxylic acid ester - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Carboxylic acid - Organic oxide - Hydrocarbon derivative - 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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