Structure Information
Structure

Compound Identification

SMILES

OCC1OC(OC2=CC=C(C=C2)C2=COC3=C(C(O)=C(CN4CCOCC4)C(O)=C3CN3CCOCC3)C2=O)C(O)C(O)C1O

InChIKey

InChIKey=VFUPDGRCPOEQAB-UHFFFAOYSA-N

Formula

C31H38N2O12

Mass

630.647

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