Compound Identification
SMILES
CC(C)OC(=O)C1=CC=C(NC(=O)CN2C(CN3CCCC3)=NC3=C(C4=C(CCCC4)S3)C2=O)C=C1
InChIKey
InChIKey=UNYRAUVTZCIECO-UHFFFAOYSA-N
Formula
C27H32N4O4S
Mass
508.64
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
Benzoic acid esters Thienopyrimidines Anilides N-arylamides Benzoyl derivatives Pyrimidones Aralkylamines N-alkylpyrrolidines Thiophenes Heteroaromatic compounds Trialkylamines Secondary carboxylic acid amides Amino acids and derivatives Lactams Carboxylic acid esters Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Acylaminobenzoic acid or derivatives - Benzoate ester - Anilide - Thienopyrimidine - Benzoyl - N-arylamide - Pyrimidone - Aralkylamine - Pyrimidine - N-alkylpyrrolidine - Heteroaromatic compound - Pyrrolidine - Thiophene - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Lactam - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Amine - Aromatic heteropolycyclic 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