Structure Information
Structure

Compound Identification

SMILES

[K+].[K+].COC1=C(O)C=CC(=C1)C1=C(OS([O-])(=O)=O)C(=O)C2=C(O)C=C(OS([O-])(=O)=O)C=C2O1

InChIKey

InChIKey=JILXHFDBMPFPLQ-UHFFFAOYSA-L

Formula

C16H10K2O13S2

Mass

552.56

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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 - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Chromone - Benzopyran - Arylsulfate - Methoxyphenol - 1-benzopyran - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Pyranone - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Sulfuric acid ester - Pyran - Sulfuric acid monoester - Sulfate-ester - Organic sulfuric acid or derivatives - Heteroaromatic compound - Vinylogous acid - Oxacycle - Ether - Organic alkali metal salt - Organoheterocyclic compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic potassium salt - Organic salt - Organic cation - 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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