Structure Information
Structure

Compound Identification

SMILES

[H]\C(=C(\[H])C1=CC(OC)=C(O)C=C1)C(=O)O[C@]1([H])[C@@]([H])(O)[C@]([H])(O)[C@@]([H])(CO)O[C@@]1([H])C1=C(O)C=C(C)C2=C1O[C@]([H])(CC(C)=O)CC2=O

InChIKey

InChIKey=URPBWFLWFIMWFY-RDKROQLNSA-N

Formula

C29H32O12

Mass

572.563

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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 - Hydroxycinnamic acid or derivatives - Hexose monosaccharide - Cinnamic acid ester - Coumaric acid or derivatives - Cinnamic acid or derivatives - C-glycosyl compound - Chromone - Methoxyphenol - 1-benzopyran - Chromane - Benzopyran - Phenoxy compound - Phenol ether - Styrene - Anisole - Aryl ketone - Aryl alkyl ketone - Methoxybenzene - Phenol - Alkyl aryl ether - Fatty acid ester - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Oxane - Monosaccharide - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Secondary alcohol - Carboxylic acid ester - Ketone - Ether - Dialkyl ether - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organic oxide - Primary alcohol - Carbonyl group - 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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