Compound Identification
SMILES
COC1=C(C=C2C=C(Br)C=CC2=N1)C(C1=CC=CC=C1)C(O)(CSCCN(C)C)C1=CC=CC=C1
InChIKey
InChIKey=XZPKVDSNSUBIQC-UHFFFAOYSA-N
Formula
C29H31BrN2O2S
Mass
551.54
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
Quinolones and derivatives Haloquinolines Alkyl aryl ethers Pyridines and derivatives Benzene and substituted derivatives Aryl bromides Tertiary alcohols Heteroaromatic compounds Trialkylamines Sulfenyl compounds Dialkylthioethers Azacyclic compounds Organobromides Hydrocarbon derivatives Aromatic alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Stilbene - Haloquinoline - Quinolone - Quinoline - Alkyl aryl ether - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Pyridine - Benzenoid - Heteroaromatic compound - Tertiary alcohol - Tertiary aliphatic amine - Tertiary amine - Azacycle - Ether - Organoheterocyclic compound - Dialkylthioether - Sulfenyl compound - Thioether - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic nitrogen compound - Alcohol - Organosulfur compound - Amine - Organic oxygen compound - Aromatic alcohol - Hydrocarbon derivative - 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