Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)[C@H]1OC2=C3C4[C@@H](O)[C@@](OC5=CC(OC)=CC(OC)=C45)(OC3=CC(OC)=C2C[C@@H]1O)C1=CC(OC)=C(OC)C=C1

InChIKey

InChIKey=LKTHMIWWFDQHGR-ASVJSXPTSA-N

Formula

C36H36O11

Mass

644.673

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Biflavonoids and polyflavonoids

Intermediate Tree Nodes

Not available

Direct Parent

Biflavonoids and polyflavonoids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

A-type proanthocyanidin - Bi- and polyflavonoid skeleton - Proanthocyanidin - Catechin - Pyranoflavonoid - 3p-methoxyflavonoid-skeleton - 4p-methoxyflavonoid-skeleton - 5-methoxyflavonoid-skeleton - 7-methoxyflavonoid-skeleton - 3-hydroxyflavonoid - Flavan-3-ol - Hydroxyflavonoid - Flavan - Pyranochromene - Chromane - Benzopyran - O-dimethoxybenzene - Dimethoxybenzene - 1-benzopyran - Anisole - Methoxybenzene - Phenol ether - Phenoxy compound - Alkyl aryl ether - Ketal - Monocyclic benzene moiety - Benzenoid - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Acetal - Ether - Organooxygen compound - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''.

External Descriptors

Not available

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