Structure Information
Structure

Compound Identification

SMILES

COC1=C(O)C=CC(=C1)[C@H]1OC[C@H]2[C@@H]1CO[C@@H]2C1=CC(OC)=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1

InChIKey

InChIKey=HPFDJXJQLWQMOR-HGBPNTTHSA-N

Formula

C32H42O16

Mass

682.672

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lignans, neolignans and related compounds

Class

Lignan glycosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Lignan glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Lignan glycoside - Furanoid lignan - Furofuran lignan skeleton - Fatty acyl glycoside of mono- or disaccharide - Phenolic glycoside - Fatty acyl glycoside - Alkyl glycoside - Glycosyl compound - O-glycosyl compound - Disaccharide - Methoxyphenol - Phenoxy compound - Anisole - Phenol ether - Furofuran - Methoxybenzene - Phenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Oxane - Monocyclic benzene moiety - Fatty acyl - Oxolane - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Polyol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Alcohol - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.

External Descriptors

Not available

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