Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C11H14N2O2 |
| Molecular Weight | 206.2411 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(C(=O)NC(N)=O)C1=CC=CC=C1
InChI
InChIKey=AJOQSQHYDOFIOX-UHFFFAOYSA-N
InChI=1S/C11H14N2O2/c1-2-9(10(14)13-11(12)15)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3,(H3,12,13,14,15)
| Molecular Formula | C11H14N2O2 |
| Molecular Weight | 206.2411 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
DescriptionCurator's Comment: Description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/529017
Curator's Comment: Description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/529017
Pheneturide ((brand names Benuride, Deturid, Pheneturid, Septotence, Trinuride), a decarboxylation product of phenobarbital, has been shown to be an effective drug against seizures, and in particular psychomotor seizures. It has being marketed in Europe, including in Poland, Spain, and the United Kingdom. Pheneturide is supplied in compressed tablets each containing 200 mg. of the drug. It can also be obtained in compound tablets (" trinuride ') each of which contain 200 mg. of pheneturide, 40 mg. of diphenylhydantoin, and 15 mg. of phenobarbitone. Animal experiments have shown that pheneturide protects against drug-induced and electrically induced convulsions.
Approval Year
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
Sources: http://www.ndrugs.com/?s=laburide |
Primary | Laburide Approved UseIndications: epilepsy |
Doses
| Dose | Population | Adverse events |
|---|---|---|
200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
Disc. AE: Trance, Constipation... Other AEs: Drowsiness, Ataxia... AEs leading to discontinuation/dose reduction: Trance (2.27%) Other AEs:Constipation (2.27%) Erythematous rash (2.27%) Drowsiness (29.5%) Sources: Ataxia (29.5%) Anorexia (4.5%) Dysarthria (4.5%) Vertigo (4.5%) Headache (4.5%) |
200 mg 3 times / day multiple, oral Studied dose Dose: 200 mg, 3 times / day Route: oral Route: multiple Dose: 200 mg, 3 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
Other AEs: Drowsiness, Depression... Other AEs: Drowsiness Sources: Depression Rash (18.75%) Headache (16.7%) Dizziness (20.8%) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Constipation | 2.27% Disc. AE |
200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Erythematous rash | 2.27% Disc. AE |
200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Trance | 2.27% Disc. AE |
200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Ataxia | 29.5% | 200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Drowsiness | 29.5% | 200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Anorexia | 4.5% | 200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Dysarthria | 4.5% | 200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Headache | 4.5% | 200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Vertigo | 4.5% | 200 mg 5 times / day multiple, oral Highest studied dose Dose: 200 mg, 5 times / day Route: oral Route: multiple Dose: 200 mg, 5 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Depression | 200 mg 3 times / day multiple, oral Studied dose Dose: 200 mg, 3 times / day Route: oral Route: multiple Dose: 200 mg, 3 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
|
| Drowsiness | 200 mg 3 times / day multiple, oral Studied dose Dose: 200 mg, 3 times / day Route: oral Route: multiple Dose: 200 mg, 3 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
|
| Headache | 16.7% | 200 mg 3 times / day multiple, oral Studied dose Dose: 200 mg, 3 times / day Route: oral Route: multiple Dose: 200 mg, 3 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Rash | 18.75% | 200 mg 3 times / day multiple, oral Studied dose Dose: 200 mg, 3 times / day Route: oral Route: multiple Dose: 200 mg, 3 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Dizziness | 20.8% | 200 mg 3 times / day multiple, oral Studied dose Dose: 200 mg, 3 times / day Route: oral Route: multiple Dose: 200 mg, 3 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 18:28:15 GMT 2025
by
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Mon Mar 31 18:28:15 GMT 2025
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| Record UNII |
878CEJ4HGX
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WHO-VATC |
QN03AX13
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C264
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WHO-ATC |
N03AX13
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m8614
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C005825
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CHEMBL2107062
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100000082233
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878CEJ4HGX
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DB13362
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PHENETURIDE
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6509-31-5
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201-998-2
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