Compound Identification
SMILES
OCC1=CC=C(C=C1)C1CC(CN2CCC(O)C2)OC(O1)C1=CC=C(NC(=O)CCCC(O)=O)C=C1
InChIKey
InChIKey=PVKSTZHXZANDFT-UHFFFAOYSA-N
Formula
C27H34N2O7
Mass
498.576
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
- Subclass Anilides
-
Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Anilides
Intermediate Tree Nodes
Not available
Direct Parent
Anilides
Alternative Parents
N-arylamides Benzyl alcohols Aralkylamines 1,3-dioxanes N-alkylpyrrolidines Fatty amides Trialkylamines Secondary carboxylic acid amides Secondary alcohols 1,2-aminoalcohols Amino acids Oxacyclic compounds Acetals Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Aromatic alcohols Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - Benzyl alcohol - N-arylamide - Aralkylamine - Meta-dioxane - Fatty amide - N-alkylpyrrolidine - Fatty acyl - Pyrrolidine - 1,2-aminoalcohol - Amino acid or derivatives - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Amino acid - Azacycle - Oxacycle - Organoheterocyclic compound - Acetal - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Amine - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Carbonyl group - Organic nitrogen compound - Aromatic alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.
External Descriptors
Not available