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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
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
Health Status: unhealthy
Age Group: 35 years
Sex: F
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
Health Status: unhealthy
Age Group: 35 years
Sex: F
Sources:
PubMed

PubMed

TitleDatePubMed
Drugs which stimulate affective behaviour. 3. Comparison of the effect of picrotoxin, pentylenetetrazol, bemigride, pipradrol, ectylurea, vanillic acid diethylamide and deanol.
1960-07
Jaundice due to ectylurea.
1958-09-18
A clinical evaluation of ectylurea (nostyn).
1958-02-15
A new compound for the symptomatic treatment of tension and anxiety: 2-ethylcrotonylurea (nostyn).
1956-10
Name Type Language
ECTYLUREA
INN   MI   WHO-DD  
INN  
Official Name English
ASTYN
Preferred 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
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 Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
Code System Code Type Description
MERCK INDEX
m714
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY Merck Index
NCI_THESAURUS
C76939
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
CAS
5982-97-8
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
FDA UNII
1U73ZZU4JK
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
SMS_ID
100000080489
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
CAS
95-04-5
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
PUBCHEM
5895404
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
ECHA (EC/EINECS)
227-794-3
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
INN
237
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID201018991
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
NSC
169502
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
ChEMBL
CHEMBL1908316
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-386-8
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
DRUG CENTRAL
984
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
EVMPD
SUB06452MIG
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY
NSC
163913
Created by admin on Mon Mar 31 17:55:21 GMT 2025 , Edited by admin on Mon Mar 31 17:55:21 GMT 2025
PRIMARY