Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](OC2=CC(O)=C(CN3CCCC3C(O)=O)C(O)=C2C(=O)CCC2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=UMDWGQGNCIHUFP-ZYTSYGECSA-N

Formula

C27H33NO12

Mass

563.556

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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 - Proline or derivatives - Alkyl-phenylketone - Hexose monosaccharide - Butyrophenone - Glycosyl compound - O-glycosyl compound - Alpha-amino acid - Alpha-amino acid or derivatives - Phenylketone - Phenoxy compound - Benzoyl - Benzylamine - Phenol ether - Phenylmethylamine - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Resorcinol - Aryl ketone - Aryl alkyl ketone - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Aralkylamine - Oxane - Monocyclic benzene moiety - Benzenoid - Monosaccharide - N-alkylpyrrolidine - Pyrrolidine - Vinylogous acid - Amino acid or derivatives - Amino acid - Ketone - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Azacycle - Organoheterocyclic compound - Polyol - Oxacycle - Acetal - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Carbonyl group - Organic nitrogen compound - Aldehyde - Alcohol - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Organonitrogen compound - Amine - Organic oxide - 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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