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Details

Stereochemistry ACHIRAL
Molecular Formula C21H27N.ClH
Molecular Weight 329.907
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRAMIVERINE HYDROCHLORIDE

SMILES

Cl.CC(C)NC1CCC(CC1)(C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=BMBNXHMQMNPCIV-UHFFFAOYSA-N
InChI=1S/C21H27N.ClH/c1-17(2)22-20-13-15-21(16-14-20,18-9-5-3-6-10-18)19-11-7-4-8-12-19;/h3-12,17,20,22H,13-16H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C21H27N
Molecular Weight 293.4458
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Spasmolytic drug pramiverine was used in the active treatment of labor. In addition, it participated in clinical trials for patients with colitis syndrome. It was revealed, that pramiverine had improved the conditions of patients.

Approval Year

PubMed

PubMed

TitleDatePubMed
[The effect of the combination pramiverine/metamizole in colic pain (author's transl)].
1976-04
[Eosphagomanometric finding in man after intravenous administration of a new cholinolytic (pramiverine), atropine and scopolamine butylbromide].
1976-04
[Gaschromatographic determination of pramiverine in body fluids (author's transl)].
1976-04
[Organ distribution of 14C-pramiverine in the rat].
1976-04
Toxicological study on pramiverine (author's transl).
1976-04
[Experimental studies on pramiverine (author's transl)].
1976-04
[Animal experimental study on spasmolytic and analgesic activities of pramiverine, metamizole and their combination (author's transl)].
1976-04
[Metabolism of pramiverine (author's transl)].
1976-04
[Pharmacokinetics of pramiverine in rats, dogs, and monkeys (author's transl)].
1976-04
[On the cholinolytic activity of pramiverine].
1976-04
[Therapeutic results with the combination pramiverine/metamizole in a multicentre trial (author's transl)].
1976-04
[Pramiverine/metamizole - a spasmoanalgesic for routine therapy of symptoms in emergency/a clinical trial in patients with biliary colics (author's transl)].
1976-04
[Clinical trial of a novel spasmolytic, pramiverine, and its influence in colitis (author's transl].
1976-04
[Profile comment on clinical and experimental studies of pramiverine and pramiverine/metamizole (author's transl)].
1976-04
Effects of the spasmolytic and anticholinergic N-isopropyl-4,4-diphenylcyclohexylamine--HCl (HSp 2986) on experimental ulcer in rats.
1972-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:19:34 GMT 2025
Edited
by admin
on Mon Mar 31 19:19:34 GMT 2025
Record UNII
X23ET5815S
Record Status Validated (UNII)
Record Version
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Name Type Language
PRAMIVERIN HYDROCHLORIDE
MI  
Preferred Name English
PRAMIVERINE HYDROCHLORIDE
WHO-DD  
Common Name English
4,4-DIPHENYLCYCLOHEXYL(ISOPROPYL)AMMONIUM CHLORIDE
Systematic Name English
(4,4-DIPHENYLCYCLOHEXYL)-ISOPROPYL-AMINE HYDROCHLORIDE
Systematic Name English
PRAMIVERIN HYDROCHLORIDE [MI]
Common Name English
Pramiverine hydrochloride [WHO-DD]
Common Name English
Code System Code Type Description
PUBCHEM
197926
Created by admin on Mon Mar 31 19:19:34 GMT 2025 , Edited by admin on Mon Mar 31 19:19:34 GMT 2025
PRIMARY
FDA UNII
X23ET5815S
Created by admin on Mon Mar 31 19:19:34 GMT 2025 , Edited by admin on Mon Mar 31 19:19:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID60162395
Created by admin on Mon Mar 31 19:19:34 GMT 2025 , Edited by admin on Mon Mar 31 19:19:34 GMT 2025
PRIMARY
SMS_ID
100000085499
Created by admin on Mon Mar 31 19:19:34 GMT 2025 , Edited by admin on Mon Mar 31 19:19:34 GMT 2025
PRIMARY
CAS
14334-41-9
Created by admin on Mon Mar 31 19:19:34 GMT 2025 , Edited by admin on Mon Mar 31 19:19:34 GMT 2025
PRIMARY
MERCK INDEX
m9097
Created by admin on Mon Mar 31 19:19:34 GMT 2025 , Edited by admin on Mon Mar 31 19:19:34 GMT 2025
PRIMARY Merck Index
EVMPD
SUB04007MIG
Created by admin on Mon Mar 31 19:19:34 GMT 2025 , Edited by admin on Mon Mar 31 19:19:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
238-284-5
Created by admin on Mon Mar 31 19:19:34 GMT 2025 , Edited by admin on Mon Mar 31 19:19:34 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE