Structure Information
Structure

Compound Identification

SMILES

CC1(C)OC2=C(C=CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C2)[C@@H]([C@H]1C1=CC=CC=C1)C1=CC=C(OCCN2CCCC2)C=C1

InChIKey

InChIKey=DJZHBCYDXVEZJL-LYRFBWAMSA-N

Formula

C35H43NO8

Mass

605.728

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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

Stilbene glycoside - Neoflavonoid-7-o-glycoside - Isoflavonoid-7-o-glycoside - Isoflavonoid o-glycoside - Neoflavonoid skeleton - Neoflavan - Isoflavonoid - Isoflavonoid skeleton - Isoflavan - Phenolic glycoside - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - 2,2-dimethyl-1-benzopyran - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - 1-benzopyran - Benzopyran - Chromane - Phenol ether - Phenoxy compound - Alkyl aryl ether - Monocyclic benzene moiety - Fatty acyl - Benzenoid - N-alkylpyrrolidine - Monosaccharide - Oxane - Pyrrolidine - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Polyol - Acetal - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Alcohol - Amine - Organic nitrogen 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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