Compound Identification
SMILES
Cl.CC1=CN=C(NC(=O)C2=CC=CC=C2NC(=O)C2CCN(CC2)C2=CC=NC=C2)C=C1
InChIKey
InChIKey=IUVJMQJRHKZBAX-UHFFFAOYSA-N
Formula
C24H26ClN5O2
Mass
451.96
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Benzoic acids and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Acylaminobenzoic acid and derivatives
Alternative Parents
Anilides Benzamides Piperidinecarboxamides Benzoyl derivatives Dialkylarylamines N-arylamides Aminopyridines and derivatives Methylpyridines Imidolactams Heteroaromatic compounds Vinylogous amides Amino acids and derivatives Secondary carboxylic acid amides Azacyclic compounds Hydrochlorides Hydrocarbon derivatives Carbonyl compounds Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Acylaminobenzoic acid or derivatives - Piperidinecarboxamide - Anilide - Benzamide - Tertiary aliphatic/aromatic amine - N-arylamide - Dialkylarylamine - Benzoyl - Aminopyridine - Methylpyridine - Pyridine - Piperidine - Imidolactam - Vinylogous amide - Heteroaromatic compound - Amino acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Tertiary amine - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organonitrogen compound - Organic nitrogen compound - Amine - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Hydrochloride - Organic oxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.
External Descriptors
Not available