Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC)C=C(C=C1)C(=O)C1=C(O)C([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C(O)C=C1O

InChIKey

InChIKey=DOSNLWKBDZEVFE-RDZBXBSQSA-N

Formula

C21H24O11

Mass

452.412

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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 - Benzophenone - Diphenylmethane - Aryl-phenylketone - Hexose monosaccharide - C-glycosyl compound - Dimethoxybenzene - O-dimethoxybenzene - Benzenetriol - Phloroglucinol derivative - Methoxybenzene - Anisole - Aryl ketone - Phenoxy compound - Benzoyl - Phenol ether - Alkyl aryl ether - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Monocyclic benzene moiety - Oxane - Monosaccharide - Vinylogous acid - Secondary alcohol - Ketone - Dialkyl ether - Oxacycle - Polyol - Organoheterocyclic compound - Ether - Primary alcohol - Alcohol - Hydrocarbon derivative - Organic oxide - 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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