U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry MIXED
Molecular Formula C14H30N2O2.2I
Molecular Weight 512.2091
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIMECOLONIUM IODIDE

SMILES

[I-].[I-].CC1CCCC(C(=O)OCC[N+](C)(C)C)[N+]1(C)C

InChI

InChIKey=UZOHFHFMSPULPR-UHFFFAOYSA-L
InChI=1S/C14H30N2O2.2HI/c1-12-8-7-9-13(16(12,5)6)14(17)18-11-10-15(2,3)4;;/h12-13H,7-11H2,1-6H3;2*1H/q+2;;/p-2

HIDE SMILES / InChI

Molecular Formula C14H30N2O2
Molecular Weight 258.4002
Charge 2
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula HI
Molecular Weight 127.91241
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Dimecolonium is the N-cholinolytic drug. It is the ganglion-blocking agent. The functional activity in some ganglioid neurones increases after administration of various doses of dimecolin during the blockade and after its termination.

Approval Year

Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Rabbits data
Single dose - 10, 30 and 50 mg/kg
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:18:56 GMT 2025
Edited
by admin
on Mon Mar 31 18:18:56 GMT 2025
Record UNII
4D4NC8MXLW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIMECOLONIUM IODIDE
INN  
INN  
Official Name English
DIMEKOLIN
Preferred Name English
ESTER OF 2-CARBOXY-1,1,6-TRIMETHYLPIPERIDINIUM IODIDE WITH (2-HYDROXYETHYL) TRIMETHYLAMMONIUM IODIDE
Common Name English
dimecolonium iodide [INN]
Common Name English
DIMELIN
Common Name English
PIPERIDINIUM, 1,1,2-TRIMETHYL-6-((2-(TRIMETHYLAMMONIO)ETHOXY)CARBONYL)-, IODIDE (1:2)
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C66886
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
Code System Code Type Description
EVMPD
SUB07153MIG
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
PRIMARY
FDA UNII
4D4NC8MXLW
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
PRIMARY
EPA CompTox
DTXSID50955793
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
PRIMARY
SMS_ID
100000082633
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
PRIMARY
NCI_THESAURUS
C65394
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
PRIMARY
ChEMBL
CHEMBL2110844
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
PRIMARY
PUBCHEM
71519
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
PRIMARY
CAS
3425-97-6
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
PRIMARY
INN
1576
Created by admin on Mon Mar 31 18:18:56 GMT 2025 , Edited by admin on Mon Mar 31 18:18:56 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY