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Details

Stereochemistry ACHIRAL
Molecular Formula C18H30NO5.C7H7O3S
Molecular Weight 511.628
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TROXONIUM TOSILATE

SMILES

CC1=CC=C(C=C1)S([O-])(=O)=O.CC[N+](CC)(CC)CCOC(=O)C2=CC(OC)=C(OC)C(OC)=C2

InChI

InChIKey=LZMHPQDAYHVLMG-UHFFFAOYSA-M
InChI=1S/C18H30NO5.C7H8O3S/c1-7-19(8-2,9-3)10-11-24-18(20)14-12-15(21-4)17(23-6)16(13-14)22-5;1-6-2-4-7(5-3-6)11(8,9)10/h12-13H,7-11H2,1-6H3;2-5H,1H3,(H,8,9,10)/q+1;/p-1

HIDE SMILES / InChI

Molecular Formula C18H30NO5
Molecular Weight 340.4345
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H7O3S
Molecular Weight 171.194
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Troxonium tosylate is a triethylcholine ester which resembles hemicholinium in some of its pharmacological effects. In animal pharmacological studies, it was noted that troxonium tosylate had a marked antitremorine activity with an associated hypotensive effect. This antitremorine activity, which is a common characteristic of antiparkinsonian agents, was found to be combined with an inhibitory function on acetylcholine synthesis and with a reduction of brain catecholamines. Troxonium tosylate was found to be an effective antiparkinsonian medication for drug-induced extrapyramidal manifestations. Troxonium tosylate caused a pronounced fall in the blood pressure in both normotensive and hypertensive animals. It produced this depressor effect mainly by antagonism of both central and peripheral autonomic ganglia. Troxonium did not possess atropine-like properties and was not active as an adrenergic blocker. Despite the potent effect upon the blood pressure, it did not significantly inhibit renal function and cardiac output. Because of its unique properties, it was postulated that troxonium might be of value in the management of hypertension of various etiologies.

Approval Year

PubMed

PubMed

TitleDatePubMed
Troxonium tosylate in the treatment of drug-induced extrapyramidal manifestations.
1971 Apr

Sample Use Guides

A dose of 600 mg daily produced a significant fall in systolic and diastolic pressure relative to control levels in the hypertensives, while in the normotensives a dose of 600 mg produced no significant effect. A dosage of 1000 mg daily produced a significant fall in diastolic pressure from control levels in both these groups.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:55:16 GMT 2023
Edited
by admin
on Fri Dec 15 15:55:16 GMT 2023
Record UNII
02X87P827K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TROXONIUM TOSILATE
INN  
INN  
Official Name English
ETHANAMINIUM, N,N,N-TRIETHYL-2-((3,4,5-TRIMETHOXYBENZOYL)OXY)-, 4-METHYLBENZENESULFONATE (1:1)
Systematic Name English
NSC-96643
Code English
TRIETHYL(2-HYDROXYETHYL)AMMONIUM P-TOLUENESULFONATE 3,4,5-TRIMETHOXYBENZOATE
Common Name English
FWH-399
Code English
TROXONIUM TOSYLATE
Common Name English
troxonium tosilate [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C270
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
Code System Code Type Description
CAS
391-70-8
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
MESH
C005866
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
INN
1347
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
EPA CompTox
DTXSID30192346
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
PUBCHEM
11756111
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
NCI_THESAURUS
C152773
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
NSC
96643
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
SMS_ID
100000077466
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
ChEMBL
CHEMBL2111074
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
EVMPD
SUB11355MIG
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
FDA UNII
02X87P827K
Created by admin on Fri Dec 15 15:55:16 GMT 2023 , Edited by admin on Fri Dec 15 15:55:16 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
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ACTIVE MOIETY