Structure Information
Structure

Compound Identification

SMILES

COC1=C(O[C@@H]2O[C@H](CO[C@@H]3OC[C@](O)(CO)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)C=C2OC=C(C(=O)C2=C1O)C1=CC=C(O)C=C1

InChIKey

InChIKey=MPQNEAGCEIDBTL-OMEKLMHCSA-N

Formula

C27H30O15

Mass

594.522

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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-7-o-glycoside - Hydroxyisoflavonoid - Isoflavone - Phenolic glycoside - O-glycosyl compound - Glycosyl compound - Chromone - Disaccharide - Benzopyran - 1-benzopyran - Anisole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Pyranone - Monocyclic benzene moiety - Oxane - Pyran - Benzenoid - Vinylogous acid - Heteroaromatic compound - Oxolane - Tertiary alcohol - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Ether - Polyol - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Primary alcohol - Organic oxide - 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

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