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Structure Information
Structure

Compound Identification

SMILES

COC1=CC2=C(CN(C[C@]3(NC(=O)NC3=O)C#CC3=CC=C(C\C(C)=N\C)C=C3)C2=O)C=C1

InChIKey

InChIKey=SROAUQWBKFICCZ-HLHNIQGOSA-N

Formula

C25H24N4O4

Mass

444.491

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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 - Isoindolone - Isoindoline - Isoindole - Isoindole or derivatives - Phenylpropane - Anisole - 5-monosubstituted hydantoin - Alkyl aryl ether - Ureide - Monocyclic benzene moiety - Benzenoid - Azomethine - Dicarboximide - Tertiary carboxylic acid amide - Secondary ketimine - Lactam - Ketimine - Urea - Carboxamide group - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Carboxylic acid derivative - Ether - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Imine - Carbonyl group - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organooxygen 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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