Compound Identification
SMILES
CC(=O)NC1=CC=C(C=CC(=O)C2=C(C)N=C(S2)N2N=C(C=C2C2=CC=CC=C2)C2=CC=CC=C2)C=C1
InChIKey
InChIKey=PMOJGJXLABQDBL-UHFFFAOYSA-N
Formula
C30H24N4O2S
Mass
504.61
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Cinnamic acids and derivatives
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Cinnamic acids and derivatives
Alternative Parents
Phenylpyrazoles Acetanilides N-acetylarylamines Styrenes Aryl ketones 2,4,5-trisubstituted thiazoles Heteroaromatic compounds Enones Acryloyl compounds Acetamides Secondary carboxylic acid amides Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Cinnamic acid or derivatives - Phenylpyrazole - Acetanilide - N-acetylarylamine - Anilide - 2,4,5-trisubstituted 1,3-thiazole - Styrene - N-arylamide - Aryl ketone - Monocyclic benzene moiety - Benzenoid - Alpha,beta-unsaturated ketone - Acetamide - Heteroaromatic compound - Thiazole - Azole - Enone - Pyrazole - Acryloyl-group - Carboxamide group - Secondary carboxylic acid amide - Ketone - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid.
External Descriptors
Not available