Structure Information
Structure

Compound Identification

SMILES

COC1=CC2=C(CN(C[C@@]3(NC(=O)NC3=O)C3=CC4=C(O3)C=C(C=N4)C(\C)=N\CCN(C)C)C2=O)C=C1

InChIKey

InChIKey=LVECCXVBXQZUFD-MWMRXLLSSA-N

Formula

C26H28N6O5

Mass

504.547

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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 - Furopyridine - Isoindoline - Isoindole - Isoindole or derivatives - Anisole - 5-monosubstituted hydantoin - Alkyl aryl ether - Ureide - Pyridine - Benzenoid - Azomethine - Dicarboximide - Furan - Heteroaromatic compound - Secondary ketimine - Tertiary carboxylic acid amide - Urea - Lactam - Ketimine - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Carboxamide group - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Ether - Organooxygen compound - Organic oxygen compound - Amine - Organic oxide - Carbonyl group - Organic nitrogen compound - Organopnictogen compound - Imine - Hydrocarbon derivative - 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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