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Details

Stereochemistry ACHIRAL
Molecular Formula C7H12N2O2
Molecular Weight 156.1824
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ECTYLUREA

SMILES

CC\C(=C\C)C(=O)NC(N)=O

InChI

InChIKey=QCUPYFTWJOZAOB-HYXAFXHYSA-N
InChI=1S/C7H12N2O2/c1-3-5(4-2)6(10)9-7(8)11/h3H,4H2,1-2H3,(H3,8,9,10,11)/b5-3-

HIDE SMILES / InChI

Molecular Formula C7H12N2O2
Molecular Weight 156.1824
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

ECTYLUREA is used for the symptomatic treatment of tension and anxiety. It has no convulsant, analgesic or antispasmodic activity in animals. ECTYLUREA in therapeutic amounts has no effect on the autonomic nervous system. It also has no hypnotic effect unless given in a large dose.

Approval Year

Doses

Doses

DosePopulationAdverse events​
300 mg 3 times / day multiple, oral
Dose: 300 mg, 3 times / day
Route: oral
Route: multiple
Dose: 300 mg, 3 times / day
Sources:
unhealthy, 35 years
n = 1
Health Status: unhealthy
Condition: mild anxiety
Age Group: 35 years
Sex: F
Population Size: 1
Sources:
Disc. AE: Hepatitis...
AEs leading to
discontinuation/dose reduction:
Hepatitis (1 patient)
Sources:
AEs

AEs

AESignificanceDosePopulation
Hepatitis 1 patient
Disc. AE
300 mg 3 times / day multiple, oral
Dose: 300 mg, 3 times / day
Route: oral
Route: multiple
Dose: 300 mg, 3 times / day
Sources:
unhealthy, 35 years
n = 1
Health Status: unhealthy
Condition: mild anxiety
Age Group: 35 years
Sex: F
Population Size: 1
Sources:
PubMed

PubMed

TitleDatePubMed
A clinical evaluation of ectylurea (nostyn).
1958 Feb 15
Jaundice due to ectylurea.
1958 Sep 18
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:22:00 GMT 2023
Edited
by admin
on Fri Dec 15 15:22:00 GMT 2023
Record UNII
1U73ZZU4JK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ECTYLUREA
INN   MI   WHO-DD  
INN  
Official Name English
Ectylurea [WHO-DD]
Common Name English
ECTYLCARBAMIDE
Common Name English
CRONIL
Brand Name English
NEUROPROCIN
Brand Name English
(Z)-N-(AMINOCARBONYL)-2-ETHYL-2-BUTENAMIDE
Systematic Name English
EKTYL
Brand Name English
NOSTAL
Brand Name English
(Z)-(.ALPHA.-ETHYLCROTONYL)CARBAMIDE
Common Name English
NOSTYN
Brand Name English
2-BUTENAMIDE, N-(AMINOCARBONYL)-2-ETHYL-, (Z)-
Systematic Name English
ASTYN
Brand Name English
UREA, (2-ETHYLCROTONOYL)-, CIS-
Common Name English
2-BUTENAMIDE, N-(AMINOCARBONYL)-2-ETHYL-
Systematic Name English
ectylurea [INN]
Common Name English
CIS-(2-ETHYLCROTONYL)UREA
Common Name English
PACETYN
Brand Name English
ECTYLUREA [MI]
Common Name English
LEVANIL
Brand Name English
NSC-163913
Code English
(2-ETHYLCROTONYL)UREA
Systematic Name English
NSC-169502
Code English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
Code System Code Type Description
MERCK INDEX
m714
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C76939
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
CAS
5982-97-8
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
FDA UNII
1U73ZZU4JK
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
SMS_ID
100000080489
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
CAS
95-04-5
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
PUBCHEM
5895404
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
ECHA (EC/EINECS)
227-794-3
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
INN
237
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
EPA CompTox
DTXSID0049024
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
NSC
169502
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
ChEMBL
CHEMBL1908316
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-386-8
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
DRUG CENTRAL
984
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
EVMPD
SUB06452MIG
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
NSC
163913
Created by admin on Fri Dec 15 15:22:00 GMT 2023 , Edited by admin on Fri Dec 15 15:22:00 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY