Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2OC2=CC(O)=C(C(=O)CCC3=CC(O)=C(O)C=C3)C(O)=C2)[C@H](O)[C@H](O)[C@H]1O

InChIKey

InChIKey=CPADUELZCFSWDX-PYXJVEIZSA-N

Formula

C27H34O15

Mass

598.554

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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 heteromonocyclic compounds

Substituents

Flavonoid o-glycoside - 2'-hydroxy-dihydrochalcone - Phenolic glycoside - Cinnamylphenol - Linear 1,3-diarylpropanoid - Alkyl-phenylketone - O-glycosyl compound - Glycosyl compound - Disaccharide - Butyrophenone - Phenylketone - Phenoxy compound - Aryl alkyl ketone - Aryl ketone - Resorcinol - Phenol ether - Catechol - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Oxane - Monocyclic benzene moiety - Vinylogous acid - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aromatic heteromonocyclic 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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