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Details

Stereochemistry ACHIRAL
Molecular Formula C21H27N
Molecular Weight 293.4458
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRAMIVERINE

SMILES

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

InChI

InChIKey=SBEOBYJLAQKTQX-UHFFFAOYSA-N
InChI=1S/C21H27N/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

HIDE SMILES / InChI

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 18:01:10 GMT 2025
Edited
by admin
on Mon Mar 31 18:01:10 GMT 2025
Record UNII
157NY06G9T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SISTALGINA
Preferred Name English
PRAMIVERINE
INN   WHO-DD  
INN  
Official Name English
EMD-9806
Code English
HSP-2986
Code English
HSP 2986
Code English
pramiverine [INN]
Common Name English
PRAMIVERIN [MI]
Common Name English
Pramiverine [WHO-DD]
Common Name English
EMD 9806
Code English
Classification Tree Code System Code
NCI_THESAURUS C29698
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
Code System Code Type Description
MERCK INDEX
m9097
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY Merck Index
FDA UNII
157NY06G9T
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
SMS_ID
100000081414
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
EPA CompTox
DTXSID00162394
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
CAS
14334-40-8
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105259
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
MESH
C100133
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
RXCUI
190433
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY RxNorm
PUBCHEM
71681
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
NCI_THESAURUS
C73175
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
EVMPD
SUB09992MIG
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
DRUG CENTRAL
2235
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
INN
2581
Created by admin on Mon Mar 31 18:01:10 GMT 2025 , Edited by admin on Mon Mar 31 18:01:10 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY