Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1CO[C@@H](OC2=C3C[C@H](O)[C@@H](OC3=CC(O)=C2)C2=CC(O)=C(O)C=C2)[C@H](O)[C@H]1OCCO[C@H]1[C@H](O)CO[C@@H](OC2=C3C[C@@H](O)[C@H](OC3=CC(O)=C2)C2=CC(O)=C(O)C=C2)[C@@H]1O

InChIKey

InChIKey=UVSLMQOLLBAJTK-PTQAOEBPSA-N

Formula

C42H46O20

Mass

870.81

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Flavonoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonoid-5-o-glycoside - Flavonoid o-glycoside - Catechin - 3'-hydroxyflavonoid - 3-hydroxyflavonoid - 4'-hydroxyflavonoid - 7-hydroxyflavonoid - Flavan-3-ol - Hydroxyflavonoid - Flavan - Phenolic glycoside - Glycosyl compound - O-glycosyl compound - Chromane - Benzopyran - 1-benzopyran - Catechol - Phenol - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monosaccharide - Benzenoid - Oxane - Monocyclic benzene moiety - Secondary alcohol - Organoheterocyclic compound - Acetal - Ether - Dialkyl ether - Oxacycle - Alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid o-glycosides. These are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.

External Descriptors

Not available

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