Structure Information
Structure

Compound Identification

SMILES

[H][C@@]1(CO)O[C@@]([H])([C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O)[C@]1(OC2=CC=C(C=C2)C2=COC3=CC4=C(OCO4)C(OC)=C3C2=O)O[C@@]([H])(CO)[C@]([H])(O)[C@@]([H])(O)[C@]1([H])O

InChIKey

InChIKey=RAXJJMYJHQSVHF-JOPFZCMGSA-N

Formula

C29H32O16

Mass

636.559

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 o-glycoside - Isoflavonoid-4p-o-glycoside - Isoflavone - Phenolic glycoside - C-glycosyl compound - Chromone - Glycosyl compound - Benzopyran - 1-benzopyran - Benzodioxole - Phenoxy compound - Anisole - Phenol ether - Alkyl aryl ether - Ketal - Pyranone - Monocyclic benzene moiety - Benzenoid - Pyran - Monosaccharide - Oxane - Vinylogous ester - Heteroaromatic compound - Secondary alcohol - Ether - Dialkyl ether - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Primary alcohol - 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