Structure Information
Structure

Compound Identification

SMILES

[H][C@@]1(O)CC2=C(O[C@@]1([H])C1=CC(O)=C(O)C=C1)C(=C(O)C=C2O)[C@@]1([H])C2=C(O)C=C(O)C(=C2O[C@]([H])(C2=CC(OC(=O)C3=CC(O)=C(O)C(O)=C3)=C(OC(=O)C3=CC(O)=C(O)C(O)=C3)C(OC(=O)C3=CC(O)=C(O)C(O)=C3)=C2)[C@@]1([H])O)[C@@]1([H])C2=C(O)C=C(O)C=C2O[C@]([H])(C2=CC(O)=C(O)C=C2)[C@@]1([H])O

InChIKey

InChIKey=NBDSERKPLXKKBN-DPKJFSKGSA-N

Formula

C66H50O31

Mass

1339.095

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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 - Hydrolyzable tannin - Epigallocatechin - Depside backbone - Catechin - 3'-hydroxyflavonoid - Hydroxyflavonoid - 7-hydroxyflavonoid - 5-hydroxyflavonoid - 4'-hydroxyflavonoid - Flavan-3-ol - 3-hydroxyflavonoid - Tannin - Flavan - Galloyl ester - Gallic acid or derivatives - M-hydroxybenzoic acid ester - P-hydroxybenzoic acid ester - Benzopyran - Chromane - Phenol ester - Benzoate ester - 1-benzopyran - Pyrogallol derivative - Tricarboxylic acid or derivatives - Benzoic acid or derivatives - Benzenetriol - Benzoyl - Catechol - Phenoxy compound - Phenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Benzenoid - Monocyclic benzene moiety - Carboxylic acid ester - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Ether - Polyol - Carboxylic acid derivative - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Alcohol - Organic oxygen compound - 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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