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Details

Stereochemistry UNKNOWN
Molecular Formula C17H36N2
Molecular Weight 268.4811
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 4
E/Z Centers 0
Charge 2

SHOW SMILES / InChI
Structure of TRIMETHIDINIUM

SMILES

CC1(C)C2CCC1(C)C[N+](C)(CCC[N+](C)(C)C)C2

InChI

InChIKey=GPUGLFZXYGTLBI-UHFFFAOYSA-N
InChI=1S/C17H36N2/c1-16(2)15-9-10-17(16,3)14-19(7,13-15)12-8-11-18(4,5)6/h15H,8-14H2,1-7H3/q+2

HIDE SMILES / InChI

Molecular Formula C17H36N2
Molecular Weight 268.4811
Charge 2
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Trimethidinium is a bisquaternary amine ganglion blocking agent with antihypertensive actions. Administration of the drug results in a decrease in blood pressure in the systemic and pulmonary arteries and the right atrium. Associated with these decreased pressures, the stroke volume decreased, but there was sufficient increase in cardiac rate so that cardiac output did not change significantly. Both right and left ventricular work decreased significantly while left ventricular myocardial oxygen consumption was unchanged and calculated cardiac efficiency decreased. Associated side effects on the gastrointestinal tract are reported to be mild and easily controlled when compared with those of pentapyrrolidinium and mecamylamine.

Approval Year

Doses

Doses

DosePopulationAdverse events​
300 mg 1 times / day steady, oral
Studied dose
Dose: 300 mg, 1 times / day
Route: oral
Route: steady
Dose: 300 mg, 1 times / day
Sources:
unhealthy, 19-61 years
Health Status: unhealthy
Age Group: 19-61 years
Sex: M+F
Sources:
Other AEs: Paralytic ileus, Constipation...
Other AEs:
Paralytic ileus (1 patient)
Constipation (mild, 1 patient)
Sources:
AEs

AEs

AESignificanceDosePopulation
Paralytic ileus 1 patient
300 mg 1 times / day steady, oral
Studied dose
Dose: 300 mg, 1 times / day
Route: oral
Route: steady
Dose: 300 mg, 1 times / day
Sources:
unhealthy, 19-61 years
Health Status: unhealthy
Age Group: 19-61 years
Sex: M+F
Sources:
Constipation mild, 1 patient
300 mg 1 times / day steady, oral
Studied dose
Dose: 300 mg, 1 times / day
Route: oral
Route: steady
Dose: 300 mg, 1 times / day
Sources:
unhealthy, 19-61 years
Health Status: unhealthy
Age Group: 19-61 years
Sex: M+F
Sources:
PubMed

PubMed

TitleDatePubMed
[Effect of hypotensive agents on return of venous blood to the heart].
1982-03-01
Vasopressin and beta-endorphin release after osmotic and non-osmotic stimuli: effect of naloxone and dexamethasone.
1982-02-05
Effect of isoprenaline and trimethidinium on the plasma vasopressin concentration in conscious rats.
1980-06
[Double controlled regulation of renin release by the sympathetic nervous system. Stimulation via beta receptors and inhibition via alpha receptors].
1977-09-29
alpha-Adrenoceptor-mediated inhibitory effect of the sympathetic nervous system on the isoprenaline-induced increase in plasma renin concentration.
1977-08
Cholinergic agents affect two receptors that modulate transmitter release at a central synapse in Aplsia californica.
1975-05-09
[TREATMENT OF HYPERTENSION WITH CAMPHONIUM].
1963-10
Acute systemic and coronary hemodynamic effects of trimethidinium methosulfate.
1962-05
[On the pharmacology of Camphonium].
1962-03-01
A controlled clinical comparison of guanethidine and trimethidinium methosulfate.
1962-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:10:03 GMT 2025
Edited
by admin
on Mon Mar 31 21:10:03 GMT 2025
Record UNII
FZ7142TV3J
Record Status Validated (UNII)
Record Version
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Name Type Language
TRIMETHIDENIUM
Preferred Name English
TRIMETHIDINIUM
Common Name English
TRIMETHIDINIUM CATION
Common Name English
1,3,8,8-TETRAMETHYL-3-(3-(TRIMETHYLAMMONIO)PROPYL)-3-AZONIABICYCLO(3.2.1)OCTANE
Systematic Name English
TRIMETHIDINIUM ION
Common Name English
Code System Code Type Description
FDA UNII
FZ7142TV3J
Created by admin on Mon Mar 31 21:10:03 GMT 2025 , Edited by admin on Mon Mar 31 21:10:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID0048424
Created by admin on Mon Mar 31 21:10:03 GMT 2025 , Edited by admin on Mon Mar 31 21:10:03 GMT 2025
PRIMARY
PUBCHEM
26484
Created by admin on Mon Mar 31 21:10:03 GMT 2025 , Edited by admin on Mon Mar 31 21:10:03 GMT 2025
PRIMARY
DRUG CENTRAL
3845
Created by admin on Mon Mar 31 21:10:03 GMT 2025 , Edited by admin on Mon Mar 31 21:10:03 GMT 2025
PRIMARY
CAS
2624-50-2
Created by admin on Mon Mar 31 21:10:03 GMT 2025 , Edited by admin on Mon Mar 31 21:10:03 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY