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Details

Stereochemistry RACEMIC
Molecular Formula C11H12N2O2
Molecular Weight 204.2252
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYLPHENYLHYDANTOIN

SMILES

CCC1(NC(=O)NC1=O)C2=CC=CC=C2

InChI

InChIKey=UDTWZFJEMMUFLC-UHFFFAOYSA-N
InChI=1S/C11H12N2O2/c1-2-11(8-6-4-3-5-7-8)9(14)12-10(15)13-11/h3-7H,2H2,1H3,(H2,12,13,14,15)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
P-450 enzyme induction by 5-ethyl-5-phenylhydantoin and 5,5-diethylhydantoin, analogues of barbiturate tumor promoters phenobarbital and barbital, and promotion of liver and thyroid carcinogenesis initiated by N-nitrosodiethylamine in rats.
1988 May 1
Assessment of urinary mephenytoin metrics to phenotype for CYP2C19 and CYP2B6 activity.
2008 Apr
Name Type Language
ETHYLPHENYLHYDANTOIN
Systematic Name English
NIRVANOL
Brand Name English
5-PHENYL-5-ETHYLHYDANTOIN
Systematic Name English
HYDANTOIN, 5-ETHYL-5-PHENYL-
Systematic Name English
2,4-IMIDAZOLIDINEDIONE, 5-ETHYL-5-PHENYL-
Systematic Name English
5,5-PHENYLETHYLHYDANTOIN
Common Name English
NSC-150466
Code English
5-ETHYL-5-PHENYLHYDANTOIN
Systematic Name English
NSC-33388
Code English
5-ETHYL-5-PHENYL-2,4-IMIDAZOLIDINEDIONE
Systematic Name English
(RS)-5-ETHYL-5-PHENYL-2,4-IMIDAZOLIDINEDIONE
Systematic Name English
DESMETHYLMEPHENYTOIN
Common Name English
NORMEPHENYTOIN
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID80874185
Created by admin on Sat Dec 16 08:13:52 GMT 2023 , Edited by admin on Sat Dec 16 08:13:52 GMT 2023
PRIMARY
NSC
33388
Created by admin on Sat Dec 16 08:13:52 GMT 2023 , Edited by admin on Sat Dec 16 08:13:52 GMT 2023
PRIMARY
WIKIPEDIA
Nirvanol
Created by admin on Sat Dec 16 08:13:52 GMT 2023 , Edited by admin on Sat Dec 16 08:13:52 GMT 2023
PRIMARY
PUBCHEM
91480
Created by admin on Sat Dec 16 08:13:52 GMT 2023 , Edited by admin on Sat Dec 16 08:13:52 GMT 2023
PRIMARY
CAS
631-07-2
Created by admin on Sat Dec 16 08:13:52 GMT 2023 , Edited by admin on Sat Dec 16 08:13:52 GMT 2023
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NSC
150466
Created by admin on Sat Dec 16 08:13:52 GMT 2023 , Edited by admin on Sat Dec 16 08:13:52 GMT 2023
PRIMARY
ECHA (EC/EINECS)
211-150-3
Created by admin on Sat Dec 16 08:13:52 GMT 2023 , Edited by admin on Sat Dec 16 08:13:52 GMT 2023
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FDA UNII
23SM1FA1AK
Created by admin on Sat Dec 16 08:13:52 GMT 2023 , Edited by admin on Sat Dec 16 08:13:52 GMT 2023
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