Structure Information
Structure

Compound Identification

SMILES

[H]C1(CO)OC([H])(OC2([H])C([H])(O)C([H])(CO)OC([H])(OC3=C(OC)C=C4C(=O)C(=COC4=C3)C3=CC(OC)=C(OC)C=C3)C2([H])O)C([H])(O)C([H])(O)C1([H])O

InChIKey

InChIKey=XXSWXJGGMRMITA-UHFFFAOYSA-N

Formula

C30H36O16

Mass

652.602

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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 - 3p-methoxyisoflavone - 4p-o-methylisoflavone - Isoflavone - Phenolic glycoside - Chromone - Disaccharide - Glycosyl compound - O-glycosyl compound - Benzopyran - O-dimethoxybenzene - Dimethoxybenzene - 1-benzopyran - Phenol ether - Anisole - Phenoxy compound - Methoxybenzene - Pyranone - Alkyl aryl ether - Pyran - Benzenoid - Oxane - Monocyclic benzene moiety - Heteroaromatic compound - Secondary alcohol - Organoheterocyclic compound - Ether - Acetal - Polyol - Oxacycle - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Alcohol - 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

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