Structure Information
Structure

Compound Identification

SMILES

O[C@H]1[C@H](OC2=CC(O)=CC(O)=C2C1C1=C2O[C@@H]([C@H](O)C(C3=C4O[C@@H]([C@H](O)C(C5=C(O)C=C(O)C6=C5O[C@@H]([C@H](O)C6C5=C(O)C=C(O)C6=C5O[C@@H]([C@H](O)C6C5=C(O)C=C(O)C6=C5O[C@@H]([C@H](C6)OC(=O)C5=CC(O)=C(O)C(O)=C5)C5=CC(O)=C(O)C=C5)C5=CC(O)=C(O)C=C5)C5=CC(O)=C(O)C=C5)C4=C(O)C=C3O)C3=CC(O)=C(O)C=C3)C2=C(O)C=C1O)C1=CC(O)=C(O)C=C1)C1=CC(O)=C(O)C=C1

InChIKey

InChIKey=UJPAMFHQFNUCFR-SKUOXQEWSA-N

Formula

C97H78O40

Mass

1883.651

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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

C-type proanthocyanidin - B-type proanthocyanidin - Proanthocyanidin - Bi- and polyflavonoid skeleton - Catechin gallate - Catechin - Hydroxyflavonoid - Flavan-3-ol - 3'-hydroxyflavonoid - 7-hydroxyflavonoid - 5-hydroxyflavonoid - 4'-hydroxyflavonoid - 3-hydroxyflavonoid - Flavan - Galloyl ester - Gallic acid or derivatives - P-hydroxybenzoic acid ester - P-hydroxybenzoic acid alkyl ester - M-hydroxybenzoic acid ester - Benzoate ester - Chromane - Benzopyran - 1-benzopyran - Pyrogallol derivative - Benzenetriol - Benzoic acid or derivatives - Catechol - Benzoyl - Phenol - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Monocyclic benzene moiety - Secondary alcohol - Carboxylic acid ester - Polyol - Ether - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organic oxygen compound - Organic oxide - Organooxygen 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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