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Details

Stereochemistry RACEMIC
Molecular Formula C20H28N
Molecular Weight 282.443
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of EMEPRONIUM

SMILES

CC[N+](C)(C)C(C)CC(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=JEJBJBKVPOWOQK-UHFFFAOYSA-N
InChI=1S/C20H28N/c1-5-21(3,4)17(2)16-20(18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6-15,17,20H,5,16H2,1-4H3/q+1

HIDE SMILES / InChI
Emepronium bromide (Cetiprina) is a quarternary ammonium compound with anticholinergic effects. It is mainly used in the treatment of urinary frequency, urge and urge incontinence and is usually administered orally and occasionally intramuscularly. Emepronium bromide was introduced into Britain, after having been used in Sweden for a number of years. The drug was advocated especially for elderly patients suffering from nocturia and urgency with incontinence, when these were due to causes other than obstruction. It was also advocated for enuresis and hypertonic bladder states following surgery or radiotherapy.

Approval Year

PubMed

PubMed

TitleDatePubMed
Medical management of overactive bladder.
2010 Apr
Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method.
2010 Dec
[A drug seeks its disease].
2010 Jun 2-8
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Emepronium bromide is commercially available as a parenteral solution, (25 mg/ml) for intramuscular use.
Intravenous doses of 1, 5, 10 and 15 mg of emepronium bromide were given to three healthy volunteers.
Route of Administration: Intravenous
Name Type Language
EMEPRONIUM
WHO-DD  
Common Name English
Emepronium [WHO-DD]
Common Name English
ETHYLDIMETHYL(1-METHYL-3,3-DIPHENYLPROPYL)AMMONIUM
Systematic Name English
EMEPRONIUM ION
Common Name English
EMEPRONIUM CATION
Common Name English
Classification Tree Code System Code
WHO-VATC QG04BD01
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
WHO-ATC G04BD01
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
WHO-VATC QA03CA30
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
WHO-ATC N05CX05
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
WHO-VATC QN05CX05
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
WHO-ATC A03CA30
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
Code System Code Type Description
MESH
D004629
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY
SMS_ID
100000087742
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY
RXCUI
3816
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY RxNorm
DRUG BANK
DB13505
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY
CAS
27892-33-7
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY
FDA UNII
04QQ8SWA4U
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY
EPA CompTox
DTXSID701021634
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY
WIKIPEDIA
Emepronium
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY
PUBCHEM
34055
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY
EVMPD
SUB01875MIG
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY
DRUG CENTRAL
1000
Created by admin on Fri Dec 15 18:55:26 UTC 2023 , Edited by admin on Fri Dec 15 18:55:26 UTC 2023
PRIMARY