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Details

Stereochemistry RACEMIC
Molecular Formula C10H14O3S
Molecular Weight 214.281
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TOLMESOXIDE

SMILES

COC1=CC(C)=C(C=C1OC)[S+](C)[O-]

InChI

InChIKey=OZNTVIXYGTUPJY-UHFFFAOYSA-N
InChI=1S/C10H14O3S/c1-7-5-8(12-2)9(13-3)6-10(7)14(4)11/h5-6H,1-4H3

HIDE SMILES / InChI
Tolmesoxide is a member of a series of aryl sulphoxides, which were synthesized as potential anti-hypertensive agents. Studies in rats indicate that tolmesoxide lowers blood pressure by a direct relaxant effect on vascular smooth muscle. Tolmesoxide is approximately equipotent in dilating arterioles and noradrenaline constricted veins. Thus, tolmesoxide should be classified as a non-selective vasodilator. Tolmesoxide, in common with other vasodilators, has a short half-life, probably due to rapid metabolism as indicated by the early appearance of the major metabolite in the plasma. However, the relatively long duration of action (up to 12 h) contrasts with the short half-life and suggests that tolmesoxide has a specific mechanism of action of relatively long duration in the vascular walls in a manner suggested for hydralazine and minoxidil. The bioavailability of oral tolmesoxide from capsules averaged 84.5% and was independent of dose. Described side effects are: facial flushing, severe nausea, headaches and palpitations.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: vascular smooth muscle
PubMed

PubMed

TitleDatePubMed
Cardiovascular effects of intravenous tolmesoxide in hypertensive patients.
1981 Jun
Patents

Patents

Sample Use Guides

Single doses up to 600 mg
Route of Administration: Oral
Name Type Language
TOLMESOXIDE
INN  
INN  
Official Name English
4,5-DIMETHOXY-2-(METHYLSULFINYL)TOLUENE
Systematic Name English
NSC-321277
Code English
(±)-4,5-DIMETHOXY-2-(METHYLSULFINYL)TOLUENE
Systematic Name English
tolmesoxide [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C270
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
NCI_THESAURUS C29707
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
Code System Code Type Description
MESH
C016152
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
CAS
38452-29-8
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
NCI_THESAURUS
C152684
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
INN
4118
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
SMS_ID
100000077757
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
ChEMBL
CHEMBL1097904
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
FDA UNII
HHR1KHP34N
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
EVMPD
SUB11161MIG
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
PUBCHEM
72153
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID80865917
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY
NSC
321277
Created by admin on Fri Dec 15 16:50:40 GMT 2023 , Edited by admin on Fri Dec 15 16:50:40 GMT 2023
PRIMARY