Structure Information
Structure

Compound Identification

SMILES

COC1=CC(=CC([C@H](CO)[C@@H](O)C2=CC(OC)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(OC)=C2)=C1O)[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=C1

InChIKey

InChIKey=ISSOSWMYXNUMCA-QXTYCSMRSA-N

Formula

C43H56O21

Mass

908.9

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Stilbenes

Subclass

Stilbene glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Stilbene glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

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

Description

This compound belongs to the class of organic compounds known as stilbene glycosides. These are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton.

External Descriptors

Not available

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