Structure Information
Structure

Compound Identification

SMILES

CCC(C)NC(=O)C1=C(C=CC(NC(=O)C=CC2=CC=C(C=C2)[N+]([O-])=O)=C1)N1CCC2=CC=CC=C2C1

InChIKey

InChIKey=AMPILDZNVKITHG-UHFFFAOYSA-N

Formula

C29H30N4O4

Mass

498.583

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Taxonomic Classification

Taxonomy Tree

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

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Acylaminobenzoic acid or derivatives - Cinnamic acid amide - Cinnamic acid or derivatives - Aminobenzamide - Anthranilamide - Aminobenzoic acid or derivatives - Tetrahydroisoquinoline - 2-aminobenzamide - Benzamide - Nitrobenzene - Anilide - Aniline or substituted anilines - Dialkylarylamine - Nitroaromatic compound - Benzoyl - N-arylamide - Tertiary aliphatic/aromatic amine - Styrene - Aralkylamine - Vinylogous amide - Organic nitro compound - Carboxamide group - C-nitro compound - Amino acid or derivatives - Secondary carboxylic acid amide - Tertiary amine - Organoheterocyclic compound - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic oxygen compound - Organic salt - Carbonyl group - Organic oxide - Amine - Organic zwitterion - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - 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

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