Compound Identification
SMILES
ClC1=NC(SCC(=O)NC(CC2=CC=CC=C2)C2=CC=CC=C2)=NC(=C1)N1CCC(CC2=CC=CC=C2)CC1
InChIKey
InChIKey=QXXJVNNRQSMLFJ-UHFFFAOYSA-N
Formula
C32H33ClN4OS
Mass
557.15
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Stilbenes
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Stilbenes
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Stilbenes
Alternative Parents
4-benzylpiperidines Amphetamines and derivatives Dialkylarylamines Alkylarylthioethers Aminopyrimidines and derivatives Halopyrimidines Aryl chlorides Imidolactams Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Sulfenyl compounds Carbonyl compounds Organic oxides Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Stilbene - 4-benzylpiperidine - Benzylpiperidine - Amphetamine or derivatives - Aryl thioether - Dialkylarylamine - Aminopyrimidine - Halopyrimidine - Alkylarylthioether - Pyrimidine - Aryl chloride - Piperidine - Imidolactam - Benzenoid - Monocyclic benzene moiety - Aryl halide - Heteroaromatic compound - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Sulfenyl compound - Thioether - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Amine - Hydrocarbon derivative - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - Aromatic heteromonocyclic 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