Structure Information
Structure

Compound Identification

SMILES

[H][C@]1(O)CO[C@@]([H])(C2=C3OC(=CC(=O)C3=C(O)C(=C2O)[C@]2([H])O[C@]([H])(CO)[C@]([H])(O)[C@@]([H])(O)[C@]2([H])O)C2=CC=C(O)C=C2)[C@@]([H])(O)[C@]1([H])O

InChIKey

InChIKey=MMDUKUSNQNWVET-XBRPJPHBSA-N

Formula

C26H28O14

Mass

564.496

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Flavonoid C-glycosides

Direct Parent

Flavonoid 8-C-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonoid-8-c-glycoside - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Phenolic glycoside - C-glycosyl compound - Chromone - Glycosyl compound - Benzopyran - 1-benzopyran - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Pyranone - Pyran - Monocyclic benzene moiety - Oxane - Monosaccharide - Benzenoid - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Polyol - Oxacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Primary alcohol - Organic oxide - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid 8-c-glycosides. These are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone.

External Descriptors

Not available

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