Structure Information
Structure

Compound Identification

SMILES

[H][C@@]1(C)O[C@@]([H])(O[C@@]2([H])[C@]([H])(OC3=CC=C(C=C3)C3=CC(=O)C4=C(O)C=C(OC)C=C4O3)O[C@]([H])(CO[C@@]3([H])O[C@]([H])(O)[C@]([H])(O)[C@@]([H])(O)[C@]3([H])C)[C@]([H])(O)[C@]2([H])O)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O

InChIKey

InChIKey=JEQAOHBJZMHJJI-PPKWBGRBSA-N

Formula

C34H42O18

Mass

738.692

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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 o-glycoside - Flavonoid-4p-o-glycoside - 7-methoxyflavonoid-skeleton - Hydroxyflavonoid - 5-hydroxyflavonoid - Flavone - Phenolic glycoside - Glycosyl compound - O-glycosyl compound - Chromone - Disaccharide - Benzopyran - 1-benzopyran - Phenoxy compound - Anisole - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Pyranone - Monocyclic benzene moiety - Oxane - Pyran - Benzenoid - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Hemiacetal - Polyol - Ether - Organoheterocyclic compound - Oxacycle - Acetal - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Organooxygen 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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