Structure Information
Structure

Compound Identification

SMILES

OCCOC1=CC=CC=C1C1C2=CCC3C(C2CC2C(=O)N(NC4=CC=C(F)C=C4)C(=O)C12C1=CC=C(Cl)C=C1)C(=O)N(CC1=CC=CC=C1)C3=O

InChIKey

InChIKey=FDCOIMZPWGQUSI-UHFFFAOYSA-N

Formula

C41H35ClFN3O6

Mass

720.19

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Stilbenes

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Stilbenes

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Stilbene - 3-phenylpyrrolidine - Isoindolone - Isoindoline - Isoindole or derivatives - Phenoxy compound - Phenol ether - Phenylhydrazine - Alkyl aryl ether - Chlorobenzene - Fluorobenzene - Halobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Carboxylic acid imide, n-substituted - N-alkylpyrrolidine - 2-pyrrolidone - Pyrrolidone - Pyrrolidine - Pyrrole - Carboxylic acid imide - Dicarboximide - Lactam - Carboxylic acid hydrazide - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Ether - Organochloride - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Alcohol - Carbonyl group - Primary alcohol - Organohalogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

External Descriptors

Not available

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