Structure Information
Structure

Compound Identification

SMILES

[Cl-].COC1=C(O)C=CC(=C1)C1=C(O)C=C2C(O)=CC(O[C@H]3[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]3O)=CC2=[O+]1

InChIKey

InChIKey=VGVGBJDJPKKXOF-UQMNZUSNSA-N

Formula

C22H23ClO11

Mass

498.87

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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

3'-O-methylated flavonoids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

3p-methoxyflavonoid-skeleton - Hydroxyflavonoid - 5-hydroxyflavonoid - 4'-hydroxyflavonoid - 3-hydroxyflavonoid - Anthocyanidin - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Alkyl glycoside - 1-benzopyran - Methoxyphenol - Benzopyran - Phenoxy compound - Methoxybenzene - Quinomethane - Phenol ether - O-quinomethane - Anisole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkyl aryl ether - Fatty acyl - Alpha-branched alpha,beta-unsaturated-ketone - Benzenoid - Oxane - Monosaccharide - Beta-hydroxy ketone - Monocyclic benzene moiety - Heteroaromatic compound - Alpha,beta-unsaturated ketone - Enone - Acryloyl-group - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Ether - Carboximidic acid - Organic oxygen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organic zwitterion - Organooxygen compound - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 3'-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C3' atom of the flavonoid backbone.

External Descriptors

Not available

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