Compound Identification
SMILES
CC(C)C1=CC=C(C=C1)C1(Cl)N([C@H]([C@@H](N)C2=CC=CC=C2)C2=CC=CC=C2)C(=O)S1(=O)=O
InChIKey
InChIKey=JEAGPWKXWIJHFB-REQUTJCGSA-N
Formula
C25H25ClN2O3S
Mass
469.0
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
Phenylthiazetidines Monocyclic monoterpenoids Aromatic monoterpenoids Phenylpropanes Cumenes Aralkylamines Sulfones Azacyclic compounds Organochlorides Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Alkyl chlorides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Stilbene - P-cymene - Aromatic monoterpenoid - Monocyclic monoterpenoid - Phenyl-1,3-thiazetidine - Monoterpenoid - Cumene - Phenylpropane - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Sulfone - 1,3-thiazetidine - Azacycle - Organoheterocyclic compound - Alkyl chloride - Organonitrogen compound - Organochloride - Organohalogen compound - Organooxygen compound - Primary amine - Primary aliphatic amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Amine - Alkyl halide - 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