Structure Information
Structure

Compound Identification

SMILES

CC1(CO)C2CCC3(C)OC4=C(C=C(C5CC(=O)C6=C(O5)C=C(O)C=C6OC5OC(C(O)C(O)C5O)C(O)=O)C(O)=C4)C1C23

InChIKey

InChIKey=MPHHOJHVPXGLFO-UHFFFAOYSA-N

Formula

C31H34O13

Mass

614.6

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Flavonoid O-glycosides

Direct Parent

Flavonoid O-glucuronides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonoid-5-o-glucuronide - 3'-prenylated flavanone - Pyranoflavonoid - 3'-prenylated flavan - 7-hydroxyflavonoid - Flavanone - Hydroxyflavonoid - Flavan - Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Chromone - Glycosyl compound - O-glycosyl compound - 1-benzopyran - Chromane - Benzopyran - Aryl alkyl ketone - Aryl ketone - Alkyl aryl ether - Beta-hydroxy acid - 1-hydroxy-2-unsubstituted benzenoid - Pyran - Oxane - Benzenoid - Hydroxy acid - Monosaccharide - Ketone - Secondary alcohol - Acetal - Monocarboxylic acid or derivatives - Oxacycle - Polyol - Ether - Carboxylic acid - Carboxylic acid derivative - Organoheterocyclic compound - Alcohol - Organooxygen compound - Carbonyl group - Organic oxygen compound - Primary alcohol - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid o-glucuronides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid.

External Descriptors

Not available

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