CHEBI:4888 - ethotoin

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name ethotoin ChEBI ID CHEBI:4888 Definition An imidazolidine-2,4-dione that is hydantoin substituted by ethyl and phenyl at positions 3 and 5, respectively. An antiepileptic, it is less toxic than phenytoin but also less effective. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:250452 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Read full article at Wikipedia Formula C11H12N2O2 Net Charge 0 Average Mass 204.22520 Monoisotopic Mass 204.08988 InChI InChI=1S/C11H12N2O2/c1-2-13-10(14)9(12-11(13)15)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3,(H,12,15) InChIKey SZQIFWWUIBRPBZ-UHFFFAOYSA-N SMILES CCN1C(=O)NC(C1=O)c1ccccc1 Roles Classification Application(s): anticonvulsant A drug used to prevent seizures or reduce their severity. View more via ChEBI Ontology ChEBI Ontology Outgoing ethotoin (CHEBI:4888) has role anticonvulsant (CHEBI:35623) ethotoin (CHEBI:4888) is a imidazolidine-2,4-dione (CHEBI:24628) Incoming (R)-ethotoin (CHEBI:60359) is a ethotoin (CHEBI:4888) (S)-ethotoin (CHEBI:60360) is a ethotoin (CHEBI:4888) IUPAC Name 3-ethyl-5-phenylimidazolidine-2,4-dione INNs Sources ethotoin ChemIDplus ethotoine ChemIDplus ethotoinum ChemIDplus etotoina ChemIDplus Synonyms Sources (±)-3-ethyl-5-phenylhydantoin ChemIDplus 1-ethyl-2,5-dioxo-4-phenylimidazolidine ChEBI 1-ethyl-2,5-dioxo-4-phenylimidazolidine ChemIDplus 3-ethyl-5-phenyl-2,4-imidazolidinedione NIST Chemistry WebBook 3-Ethyl-5-phenyl-imidazolidine-2,4-dione ChEMBL 3-ethyl-5-phenylhydantoin ChemIDplus 3-ethyl-5-phenylimidazolidin-2,4-dione ChemIDplus Ethotoin KEGG COMPOUND Manual Xrefs Databases 1088 DrugCentral C07839 KEGG COMPOUND D00708 KEGG DRUG DB00754 DrugBank Ethotoin Wikipedia HMDB0014892 HMDB LSM-1440 LINCS US2793157 Patent View more database links Registry Numbers Types Sources 188272 Reaxys Registry Number Reaxys 86-35-1 CAS Registry Number KEGG COMPOUND 86-35-1 CAS Registry Number NIST Chemistry WebBook 86-35-1 CAS Registry Number ChemIDplus Citations Types Sources 1350205 PubMed citation Europe PMC 13553007 PubMed citation Europe PMC 6105055 PubMed citation Europe PMC 6145119 PubMed citation Europe PMC Last Modified 22 February 2017