Structure Information
Structure

Compound Identification

SMILES

CCCCC1=NC=C(\C=C2/N(CC3=CSC(C)=N3)C(=O)N(CO)C2=O)N1CC1=CC=C(C=C1)C(=O)OC

InChIKey

InChIKey=XWDLJFUUQIEWJV-JJFYIABZSA-N

Formula

C26H29N5O5S

Mass

523.61

Export to:

JSON SDF CSV

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 heteromonocyclic compounds

Substituents

Hydantoin - Alpha-amino acid or derivatives - Benzoate ester - Benzoic acid or derivatives - 1,2,5-trisubstituted-imidazole - Benzoyl - Imidazolyl carboxylic acid derivative - Trisubstituted imidazole - 2,4-disubstituted 1,3-thiazole - N-acyl urea - Ureide - Benzenoid - Monocyclic benzene moiety - N-substituted imidazole - Thiazole - Methyl ester - Azole - Dicarboximide - Heteroaromatic compound - Imidazole - Urea - Carbonic acid derivative - Carboxylic acid ester - Carboxylic acid derivative - Alkanolamine - Monocarboxylic acid or derivatives - Azacycle - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic 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

Previous Back Next