Structure Information
Structure

Compound Identification

SMILES

COC1=CC(O)=C(OC)C2=C1[C@H](C[C@@H](O2)C1=CC=CC=C1)C1=C(OC)C=C(OC)C(C(=O)\C=C\C2=CC=CC=C2)=C1O

InChIKey

InChIKey=JXGXXOHKIWFSHH-YDMGGKLESA-N

Formula

C34H32O8

Mass

568.622

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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

5-methoxyflavonoid-skeleton - 8-methoxyflavonoid-skeleton - 7-hydroxyflavonoid - 2'-hydroxychalcone - Hydroxyflavonoid - Flavan - Neoflavonoid skeleton - Neoflavan - Cinnamylphenol - Linear 1,3-diarylpropanoid - Cinnamic acid or derivatives - Methoxyphenol - Dimethoxybenzene - 1-benzopyran - M-dimethoxybenzene - Benzopyran - Chromane - Phenoxy compound - Anisole - Benzoyl - Methoxybenzene - Phenol ether - Styrene - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Monocyclic benzene moiety - Vinylogous acid - Acryloyl-group - Enone - Alpha,beta-unsaturated ketone - Ketone - Organoheterocyclic compound - Oxacycle - Ether - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - 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

Not available

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