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
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)
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
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 |
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Assessment of urinary mephenytoin metrics to phenotype for CYP2C19 and CYP2B6 activity. | 2008 Apr |
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DTXSID80874185
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33388
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211-150-3
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23SM1FA1AK
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SUBSTANCE RECORD