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Structure Information
Structure

Compound Identification

SMILES

CC1CCN(CC2=C(O)C3=C(OC=C(C3=O)C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3)C(CN3CCC(C)CC3)=C2O)CC1

InChIKey

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