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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
Effects of the spasmolytic and anticholinergic N-isopropyl-4,4-diphenylcyclohexylamine--HCl (HSp 2986) on experimental ulcer in rats.
1972 Jun
[Experimental studies on pramiverine (author's transl)].
1976 Apr
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:33:36 GMT 2023
Edited
by admin
on Fri Dec 15 15:33:36 GMT 2023
Record UNII
157NY06G9T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRAMIVERINE
INN   WHO-DD  
INN  
Official Name English
SISTALGINA
Brand 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 Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
Code System Code Type Description
MERCK INDEX
m9097
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY Merck Index
FDA UNII
157NY06G9T
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
SMS_ID
100000081414
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID00162394
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
CAS
14334-40-8
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105259
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
MESH
C100133
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
RXCUI
190433
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY RxNorm
PUBCHEM
71681
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
NCI_THESAURUS
C73175
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
EVMPD
SUB09992MIG
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
DRUG CENTRAL
2235
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
INN
2581
Created by admin on Fri Dec 15 15:33:36 GMT 2023 , Edited by admin on Fri Dec 15 15:33:36 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY