Structure Information
Structure

Compound Identification

SMILES

CCC(C)C(=O)N[C@@H]1CCCN1C(=O)[C@@H]1[C@@H](C2=CC=CC=C2)[C@@]2(OC3=CC4=C(OCO4)C(OC)=C3[C@@]1(O)[C@@H]2O)C1=CC=C(OC)C=C1

InChIKey

InChIKey=UJNLESIDKSDDSV-OHSNGIATSA-N

Formula

C36H40N2O9

Mass

644.721

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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

5-O-methylated flavonoids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5-methoxyflavonoid-skeleton - 4p-methoxyflavonoid-skeleton - Hydroxyflavonoid - 4-hydroxyflavonoid - 3-hydroxyflavonoid - Flavan - Stilbene - 1-benzopyran - Benzopyran - Chromane - Benzodioxole - Phenoxy compound - Methoxybenzene - Phenol ether - N-acylpyrrolidine - Anisole - Alkyl aryl ether - Fatty acyl - Benzenoid - N-acyl-amine - Fatty amide - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Tertiary alcohol - Pyrrolidine - Cyclic alcohol - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone.

External Descriptors

Not available

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