Structure Information
Structure

Compound Identification

SMILES

COC1=C(OCC2=CC=CC=C2)C=C(C=C1)C1=C(OS(=O)(=O)C2=CC=C(C)C=C2)C(=O)C2=C(O)C(OC)=C(OCC3=CC=CC=C3)C=C2O1

InChIKey

InChIKey=AFYCKJIXEFZKGW-UHFFFAOYSA-N

Formula

C38H32O10S

Mass

680.72

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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

6-O-methylated flavonoids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

4p-methoxyflavonoid-skeleton - 6-methoxyflavonoid-skeleton - Hydroxyflavonoid - Flavone - 5-hydroxyflavonoid - P-methylbenzenesulfonate - Chromone - Benzenesulfonate ester - Benzenesulfonate - 1-benzopyran - Benzopyran - Tosyl compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Methoxybenzene - Anisole - Phenoxy compound - Phenol ether - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Toluene - Phenol - Pyranone - Monocyclic benzene moiety - Benzenoid - Pyran - Organosulfonic acid ester - Vinylogous acid - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Oxacycle - Organoheterocyclic compound - Ether - Organic oxide - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 6-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone.

External Descriptors

Not available

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