Structure Information
Structure

Compound Identification

SMILES

CN1C(=O)NC(=CC2=CC=C(C=C2)N=C(C2C(=O)NC3=C2C=C(C=C3)[N+]([O-])=O)C2=CC=C(CCCN3CCCC3)C=C2)C1=O

InChIKey

InChIKey=QMLOGMADLAOAMI-UHFFFAOYSA-N

Formula

C33H32N6O5

Mass

592.656

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Azolidines

Subclass

Imidazolidines

Intermediate Tree Nodes

Imidazolidinones - Imidazolidinediones

Direct Parent

Hydantoins

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Hydantoin - Alpha-amino acid or derivatives - Phenylpropylamine - Indole or derivatives - Dihydroindole - Nitroaromatic compound - Aralkylamine - Ureide - Monocyclic benzene moiety - Benzenoid - N-alkylpyrrolidine - Azomethine - Pyrrolidine - Dicarboximide - Secondary ketimine - Lactam - Ketimine - Urea - Tertiary aliphatic amine - Tertiary amine - Organic nitro compound - Secondary carboxylic acid amide - Carboxamide group - Amino acid or derivatives - C-nitro compound - Carboxylic acid derivative - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic oxygen compound - Imine - Organic salt - Amine - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Organic zwitterion - Organooxygen compound - Organic oxide - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as hydantoins. These are heterocyclic compounds containing an imidazolidine substituted by ketone group at positions 2 and 4.

External Descriptors

Not available

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