Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(NN2C(=O)C3CC4C5C(CC=C4C(C4=CC=C(OCCO)C=C4)C3(C2=O)C2=CC=CC=C2)C(=O)N(C5=O)C2=CC=C(C=C2)C2=NC3=CC=CC=C3O2)C=C1

InChIKey

InChIKey=AEFFARHEOQFHAS-UHFFFAOYSA-N

Formula

C48H40N4O7

Mass

784.869

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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 - Phenyl-1,3-oxazole - 1-phenylpyrrolidine - 3-phenylpyrrolidine - Isoindolone - Benzoxazole - Isoindoline - Isoindole or derivatives - Phenoxy compound - Phenol ether - Phenylhydrazine - Alkyl aryl ether - Toluene - Monocyclic benzene moiety - Carboxylic acid imide, n-substituted - Benzenoid - Pyrrolidone - 2-pyrrolidone - Azole - Oxazole - Pyrrolidine - Pyrrole - Heteroaromatic compound - Carboxylic acid imide - Dicarboximide - Lactam - Carboxylic acid hydrazide - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Ether - Alcohol - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Primary alcohol - Organonitrogen compound - Organooxygen 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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