Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H10N2O2 |
| Molecular Weight | 178.1879 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)NC(=O)CC1=CC=CC=C1
InChI
InChIKey=XPFRXWCVYUEORT-UHFFFAOYSA-N
InChI=1S/C9H10N2O2/c10-9(13)11-8(12)6-7-4-2-1-3-5-7/h1-5H,6H2,(H3,10,11,12,13)
| Molecular Formula | C9H10N2O2 |
| Molecular Weight | 178.1879 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/22512548
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22512548
Phenacemide, also known as phenylacetylurea, is an anticonvulsant of the ureide (acetylurea) class. Phenacemide was introduced in 1949 for the treatment of epilepsy, but was eventually withdrawn from the market because of its severe side effects, which includes personality changes, blood, renal and skin disorders.
CNS Activity
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2331043 Sources: https://www.drugbank.ca/drugs/DB01121 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | PHENURONE Approved UsePhenacemide, also known as phenylacetylurea, is an anticonvulsant of the ureide (acetylurea) class. Launch Date1951 |
Doses
| Dose | Population | Adverse events |
|---|---|---|
1.5 g 1 times / day steady, oral Dose: 1.5 g, 1 times / day Route: oral Route: steady Dose: 1.5 g, 1 times / day Sources: |
unhealthy, 16 years |
Other AEs: Creatinine serum increased... |
2 g 1 times / day steady, oral Dose: 2 g, 1 times / day Route: oral Route: steady Dose: 2 g, 1 times / day Sources: |
unhealthy, 16 years |
Other AEs: Creatinine increased... |
3.5 g 1 times / day steady, oral Dose: 3.5 g, 1 times / day Route: oral Route: steady Dose: 3.5 g, 1 times / day Sources: |
unhealthy, 16 years |
Other AEs: Creatinine increased... |
2 g 1 times / day steady, oral Dose: 2 g, 1 times / day Route: oral Route: steady Dose: 2 g, 1 times / day Sources: |
unhealthy, 18 years |
Other AEs: Creatinine serum increased... |
2.5 g 1 times / day steady, oral Dose: 2.5 g, 1 times / day Route: oral Route: steady Dose: 2.5 g, 1 times / day Sources: |
unhealthy, 18 years |
Other AEs: Creatinine serum increased... |
4 g 1 times / day steady, oral Dose: 4 g, 1 times / day Route: oral Route: steady Dose: 4 g, 1 times / day Sources: |
unhealthy, 23 years |
Other AEs: Creatinine increased... |
52 ug/mL steady, oral Dose: 52 ug/mL Route: oral Route: steady Dose: 52 ug/mL Sources: |
unhealthy, children Health Status: unhealthy Age Group: children Sex: unknown Sources: |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Creatinine serum increased | 1 patient | 1.5 g 1 times / day steady, oral Dose: 1.5 g, 1 times / day Route: oral Route: steady Dose: 1.5 g, 1 times / day Sources: |
unhealthy, 16 years |
| Creatinine increased | 1 patient | 2 g 1 times / day steady, oral Dose: 2 g, 1 times / day Route: oral Route: steady Dose: 2 g, 1 times / day Sources: |
unhealthy, 16 years |
| Creatinine increased | 1 patient | 3.5 g 1 times / day steady, oral Dose: 3.5 g, 1 times / day Route: oral Route: steady Dose: 3.5 g, 1 times / day Sources: |
unhealthy, 16 years |
| Creatinine serum increased | 1 patient | 2 g 1 times / day steady, oral Dose: 2 g, 1 times / day Route: oral Route: steady Dose: 2 g, 1 times / day Sources: |
unhealthy, 18 years |
| Creatinine serum increased | 1 patient | 2.5 g 1 times / day steady, oral Dose: 2.5 g, 1 times / day Route: oral Route: steady Dose: 2.5 g, 1 times / day Sources: |
unhealthy, 18 years |
| Creatinine increased | 1 patient | 4 g 1 times / day steady, oral Dose: 4 g, 1 times / day Route: oral Route: steady Dose: 4 g, 1 times / day Sources: |
unhealthy, 23 years |
PubMed
| Title | Date | PubMed |
|---|---|---|
| The effect of acyclovir on the tubular secretion of creatinine in vitro. | 2010-12-30 |
|
| Phenacemide therapy of complex partial epilepsy in children: determination of plasma drug concentrations. | 1987-12 |
|
| The use of phenacemide for intractable partial complex epilepsy in children. | 1986-07-01 |
|
| Ouabain induced seizures: site of production and response to anticonvulsants. | 1978-11 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13451900
Phenacemide was administered orally at 500-5000 mg daily dose
Route of Administration:
Oral
| Substance Class |
Chemical
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PAI7J52V09
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Validated (UNII)
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NCI_THESAURUS |
C264
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WHO-VATC |
QN03AX07
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WHO-ATC |
N03AX07
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3380
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DB01121
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4753
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7265
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100000082226
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SUB09744MIG
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m8588
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200-570-2
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39458
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C66363
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C005396
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PAI7J52V09
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2114
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PHENACEMIDE
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DTXSID6023442
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33253
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CHEMBL918
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ACTIVE MOIETY |