Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=HAFLZKVDLUXIRO-ZHTOYOMRSA-N

Formula

C35H38N2O9

Mass

630.694

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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

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