U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of PHENACEMIDE

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)

HIDE SMILES / InChI

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

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 Phenacemide was introduced in 1949 for the treatment of epilepsy, but was eventually withdrawn from the market because of its severe side effects, which includes personality changes, blood, renal and skin disorders.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
PHENURONE

Approved Use

Phenacemide, also known as phenylacetylurea, is an anticonvulsant of the ureide (acetylurea) class.

Launch Date

1951
Doses

Doses

DosePopulationAdverse 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
n = 1
Health Status: unhealthy
Condition: psychomotor retardation
Age Group: 16 years
Sex: M
Population Size: 1
Sources:
Other AEs: Creatinine serum increased...
Other AEs:
Creatinine serum increased (1 patient)
Sources:
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
n = 1
Health Status: unhealthy
Condition: uncontrollable psychomotor epilepsy
Age Group: 16 years
Sex: M
Population Size: 1
Sources:
Other AEs: Creatinine increased...
Other AEs:
Creatinine increased (1 patient)
Sources:
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
n = 1
Health Status: unhealthy
Condition: uncontrollable psychomotor epilepsy
Age Group: 16 years
Sex: M
Population Size: 1
Sources:
Other AEs: Creatinine increased...
Other AEs:
Creatinine increased (1 patient)
Sources:
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
n = 1
Health Status: unhealthy
Condition: psychomotor retardation
Age Group: 18 years
Sex: M
Population Size: 1
Sources:
Other AEs: Creatinine serum increased...
Other AEs:
Creatinine serum increased (1 patient)
Sources:
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
n = 1
Health Status: unhealthy
Condition: psychomotor seizures
Age Group: 18 years
Sex: F
Population Size: 1
Sources:
Other AEs: Creatinine serum increased...
Other AEs:
Creatinine serum increased (1 patient)
Sources:
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
n = 1
Health Status: unhealthy
Condition: uncontrollable psychomotor epilepsy
Age Group: 23 years
Sex: M
Population Size: 1
Sources:
Other AEs: Creatinine increased...
Other AEs:
Creatinine increased (1 patient)
Sources:
52 ug/mL steady, oral
Dose: 52 ug/mL
Route: oral
Route: steady
Dose: 52 ug/mL
Sources:
unhealthy, children
n = 13
Health Status: unhealthy
Condition: complex partial seizures
Age Group: children
Sex: unknown
Population Size: 13
Sources:
AEs

AEs

AESignificanceDosePopulation
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
n = 1
Health Status: unhealthy
Condition: psychomotor retardation
Age Group: 16 years
Sex: M
Population Size: 1
Sources:
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
n = 1
Health Status: unhealthy
Condition: uncontrollable psychomotor epilepsy
Age Group: 16 years
Sex: M
Population Size: 1
Sources:
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
n = 1
Health Status: unhealthy
Condition: uncontrollable psychomotor epilepsy
Age Group: 16 years
Sex: M
Population Size: 1
Sources:
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
n = 1
Health Status: unhealthy
Condition: psychomotor retardation
Age Group: 18 years
Sex: M
Population Size: 1
Sources:
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
n = 1
Health Status: unhealthy
Condition: psychomotor seizures
Age Group: 18 years
Sex: F
Population Size: 1
Sources:
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
n = 1
Health Status: unhealthy
Condition: uncontrollable psychomotor epilepsy
Age Group: 23 years
Sex: M
Population Size: 1
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer


Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
no
Tox targets

Tox targets

TargetModalityActivityMetaboliteClinical evidence
PubMed

PubMed

TitleDatePubMed
Ouabain induced seizures: site of production and response to anticonvulsants.
1978 Nov
The use of phenacemide for intractable partial complex epilepsy in children.
1986 Jul-Aug
Phenacemide therapy of complex partial epilepsy in children: determination of plasma drug concentrations.
1987 Dec
The effect of acyclovir on the tubular secretion of creatinine in vitro.
2010 Dec 30
Patents

Sample Use Guides

Phenacemide was administered orally at 500-5000 mg daily dose
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:27:31 GMT 2023
Edited
by admin
on Fri Dec 15 16:27:31 GMT 2023
Record UNII
PAI7J52V09
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENACEMIDE
HSDB   INN   JAN   MART.   MI   ORANGE BOOK   VANDF   WHO-DD  
INN  
Official Name English
(Phenylacetyl)urea
Systematic Name English
PHENACEMIDE [VANDF]
Common Name English
PHENURONE
Brand Name English
BENZENEACETAMIDE, N-(AMINOCARBONYL)-
Systematic Name English
PHENACEMIDE [MI]
Common Name English
PHENACEMIDE [MART.]
Common Name English
phenacemide [INN]
Common Name English
Phenacemide [WHO-DD]
Common Name English
NSC-39458
Code English
PHENACEMIDE [HSDB]
Common Name English
PHENACEMIDE [ORANGE BOOK]
Common Name English
PHENACEMIDE [JAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C264
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
WHO-VATC QN03AX07
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
WHO-ATC N03AX07
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
Code System Code Type Description
HSDB
3380
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
DRUG BANK
DB01121
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
PUBCHEM
4753
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
IUPHAR
7265
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
SMS_ID
100000082226
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
EVMPD
SUB09744MIG
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
INN
92
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
MERCK INDEX
m8588
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
200-570-2
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
NSC
39458
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
NCI_THESAURUS
C66363
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
MESH
C005396
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
FDA UNII
PAI7J52V09
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
CAS
63-98-9
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
DRUG CENTRAL
2114
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
WIKIPEDIA
PHENACEMIDE
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
EPA CompTox
DTXSID6023442
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
RXCUI
33253
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY RxNorm
ChEMBL
CHEMBL918
Created by admin on Fri Dec 15 16:27:31 GMT 2023 , Edited by admin on Fri Dec 15 16:27:31 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY