Structure Information
Structure

Compound Identification

SMILES

OC1CC2=C(O)C=C(O)C(C3C(O)C(OC4=CC(O)=CC(O)=C34)C3=CC=C(O)C(O)=C3)=C2OC1C1=CC=C(O)C(OS([O-])(=O)=O)=C1

InChIKey

InChIKey=BRWPHJBCPQEKMP-UHFFFAOYSA-M

Formula

C30H25O15S

Mass

657.58

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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

B-type proanthocyanidin - Proanthocyanidin - Bi- and polyflavonoid skeleton - Catechin - Hydroxyflavonoid - Flavan-3-ol - 3'-hydroxyflavonoid - 3-hydroxyflavonoid - 7-hydroxyflavonoid - 5-hydroxyflavonoid - 4'-hydroxyflavonoid - Flavan - Phenylsulfate - Benzopyran - Chromane - Arylsulfate - 1-benzopyran - Phenoxy compound - Catechol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Sulfuric acid monoester - Sulfate-ester - Sulfuric acid ester - Monocyclic benzene moiety - Benzenoid - Organic sulfuric acid or derivatives - Secondary alcohol - Polyol - Ether - Oxacycle - Organoheterocyclic compound - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic anion - 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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