Structure Information
Structure

Compound Identification

SMILES

COC1=CC=CC(O[C@@H]2OC([C@@H](O)[C@H](O)C2O)C(O)=O)=C1[C@@H]1CC(=O)C2=C(O1)C(OC)=C(OC)C=C2O

InChIKey

InChIKey=YFJFVYFDSGLIGK-CZLOYTQASA-N

Formula

C24H26O13

Mass

522.459

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

O-methylated flavonoids

Intermediate Tree Nodes

Not available

Direct Parent

8-O-methylated flavonoids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2p-methoxyflavonoid-skeleton - 7-methoxyflavonoid-skeleton - 8-methoxyflavonoid-skeleton - 5-hydroxyflavonoid - Flavanone - Hydroxyflavonoid - Flavan - Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Chromone - Glycosyl compound - O-glycosyl compound - Chromane - Benzopyran - 1-benzopyran - Phenol ether - Aryl ketone - Anisole - Aryl alkyl ketone - Phenoxy compound - Methoxybenzene - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Beta-hydroxy acid - Oxane - Pyran - Benzenoid - Monosaccharide - Monocyclic benzene moiety - Hydroxy acid - Vinylogous acid - Secondary alcohol - Ketone - Carboxylic acid derivative - Ether - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Acetal - Polyol - Carboxylic acid - Carbonyl group - Organooxygen compound - Organic oxygen compound - Aldehyde - Alcohol - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 8-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone.

External Descriptors

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