Structure Information
Structure

Compound Identification

SMILES

CCCN=C(C)C1=C(C)C=C(C=C1)C#C[C@]1(CN2CC3=C(C=C(OC)C=C3)C2=O)NC(=O)NC1=O

InChIKey

InChIKey=CITVGCFBPBAKPO-HHHXNRCGSA-N

Formula

C27H28N4O4

Mass

472.545

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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 - Anisole - 5-monosubstituted hydantoin - Alkyl aryl ether - Ureide - Toluene - Monocyclic benzene moiety - Benzenoid - Azomethine - Dicarboximide - Secondary ketimine - Tertiary carboxylic acid amide - 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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