Structure Information
Structure

Compound Identification

SMILES

CC1CCCC[NH+]1CC1=C([O-])C(C[NH+]2CCCCC2C)=C2OC=C(C(=O)C2=C1[O-])C1=CC=C(OC2OC(CO)C(O)C(O)C2O)C=C1

InChIKey

InChIKey=VPHGNASNUHAYHV-UHFFFAOYSA-N

Formula

C35H46N2O10

Mass

654.757

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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-4p-o-glycoside - Isoflavone - Fatty acyl glycoside - Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Hexose monosaccharide - Chromone - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Phenoxy compound - Phenol ether - Aralkylamine - Phenoxide - Pyranone - Benzenoid - Monocyclic benzene moiety - Fatty acyl - Monosaccharide - Oxane - Piperidine - Pyran - Vinylogous acid - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Polyol - Oxacycle - Azacycle - Acetal - Organoheterocyclic compound - Alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic zwitterion - Primary alcohol - Organic salt - Organic oxygen compound - Amine - Organic nitrogen compound - Organonitrogen 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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