Structure Information
Structure

Compound Identification

SMILES

C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](CO)OC([C@@H]2O)C2=C(O)C=C(O)C3=C2OC(=CC3=O)C2=CC=C(OC(C)=O)C=C2)[C@@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=PASCKOABYMEVCW-BZXBQSMJSA-N

Formula

C29H32O15

Mass

620.56

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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 - Hydroxyflavonoid - Flavone - 7-hydroxyflavonoid - 5-hydroxyflavonoid - Phenolic glycoside - O-glycosyl compound - Glycosyl compound - Disaccharide - Chromone - C-glycosyl compound - 1-benzopyran - Phenol ester - Benzopyran - Phenoxy compound - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Benzenoid - Pyran - Oxane - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid derivative - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - 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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