Structure Information
Structure

Compound Identification

SMILES

OC[C@@H]1O[C@H](Oc2ccc(C3=C(O)c4ccc(O)cc4OC3=O)c(O)c2)[C@@H](O)[C@H](O)[C@H]1O

InChIKey

InChIKey=OEZWCAHAQBRTTP-QLNFFCRYSA-N

Formula

C21H20O11

Mass

448.38

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Isoflavonoids

Subclass

Isoflavonoid O-glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Isoflavonoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Isoflavonoid-4p-o-glycoside - Isoflavonoid o-glycoside - Isoflav-3-enone skeleton - Hydroxyisoflavonoid - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Phenolic glycoside - 4-hydroxycoumarin - Hexose monosaccharide - Hydroxycoumarin - Alkyl glycoside - 7-hydroxycoumarin - O-glycosyl compound - Glycosyl compound - Coumarin - Benzopyran - 1-benzopyran - Phenoxy compound - Phenol ether - Pyranone - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Oxane - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Monosaccharide - Pyran - Vinylogous acid - Heteroaromatic compound - Secondary alcohol - Lactone - Organoheterocyclic compound - Acetal - Oxacycle - Polyol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Alcohol - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.

External Descriptors

Not available

Previous Back Next