Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](OC2=CC(O)=CC(O)=C2C(=O)CCC2=CC=C(C=C2)N=[N+]=[N-])[C@H](O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=AXCDEMZKQHNYNE-OBJCFNGXSA-N

Formula

C21H23N3O9

Mass

461.427

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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 - Linear 1,3-diarylpropanoid - Phenolic glycoside - Cinnamylphenol - Alkyl-phenylketone - Hexose monosaccharide - Butyrophenone - Glycosyl compound - O-glycosyl compound - Phenylketone - Benzoyl - Phenoxy compound - Phenol ether - Phenylazide - Resorcinol - Aryl ketone - Aryl alkyl ketone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Oxane - Vinylogous acid - Azo imide - Secondary alcohol - Azo compound - Ketone - Oxacycle - Organoheterocyclic compound - Acetal - Polyol - Organic salt - Primary alcohol - Alcohol - Organic nitrogen compound - Organic zwitterion - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aldehyde - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - 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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