Structure Information
Structure

Compound Identification

SMILES

COC1=C([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2OC(=O)\C=C\C2=CC=C(O)C=C2)C2=C(C(C)=C1)C(=O)C=C(CC(C)O)O2

InChIKey

InChIKey=OUGNWRCWQLUXHX-WWGKKCKVSA-N

Formula

C29H32O11

Mass

556.564

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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 - Coumaric acid ester - Hydroxycinnamic acid or derivatives - Coumaric acid or derivatives - Cinnamic acid ester - Cinnamic acid or derivatives - C-glycosyl compound - Chromone - Benzopyran - 1-benzopyran - Anisole - Phenol ether - Styrene - Alkyl aryl ether - Phenol - Fatty acid ester - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - Fatty acyl - Monocyclic benzene moiety - Benzenoid - Pyran - Oxane - Monosaccharide - Heteroaromatic compound - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Secondary alcohol - Carboxylic acid ester - 1,2-diol - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Primary alcohol - Organic oxide - Alcohol - Carbonyl group - Hydrocarbon derivative - 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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