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Details

Stereochemistry ABSOLUTE
Molecular Formula C11H12N2S
Molecular Weight 204.291
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEXAMISOLE

SMILES

C1CN2C[C@H](N=C2S1)C3=CC=CC=C3

InChI

InChIKey=HLFSDGLLUJUHTE-JTQLQIEISA-N
InChI=1S/C11H12N2S/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10/h1-5,10H,6-8H2/t10-/m0/s1

HIDE SMILES / InChI

Molecular Formula C11H12N2S
Molecular Weight 204.291
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Dexamisole is the dextro-isomer of tetramisole, a broad spectrum anthelmintic. Dexamisole significantly improves mood and psychotonicity. In adrenergically innervated blood vessels dexamisole inhibits neuronal uptake of norepinephrine more than levamisole. Dexamisole antagonized the reserpine-induced hypothermia but was ineffective in the apomorphine-induced hypothermia in mice. It reduced ptosis produced by reserpine in mice but this effect was very weak. The effect of dexamisole on the amphetamine-induced hyperactivity depended upon the animal species. Dexamisole reduced the duration of immobility in the despair test in rats. It did not modify the 5-HTP-induced head twitch reaction in mice but produced stimulation of the hind limb flexor reflex in spinal rats. The latter effect was blocked by phenoxybenzamine but not by cyproheptadine and metergoline. Dexamisole also exerted a sedative and hypothermic effect. The above findings indicate that the pharmacological profile of dexamisole resembles in some respects that of tricyclic antidepressants; they also point out that this drug has a central noradrenergic activity.

Approval Year

PubMed

PubMed

TitleDatePubMed
Psychopharmacological profile of dexamisole.
1980 Jan-Feb

Sample Use Guides

In Vivo Use Guide
Sources: DOI: 10.1177/030006057400200214
Dosage: 50 mg three times a day
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:55:21 GMT 2023
Edited
by admin
on Sat Dec 16 17:55:21 GMT 2023
Record UNII
UMH46V5U01
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEXAMISOLE
INN   USAN  
INN   USAN  
Official Name English
TETRAMISOLE, (R)-
Common Name English
(+)-2,3,5,6-TETRAHYDRO-6-PHENYLIMIDAZO(2,1-B)THIAZOLE
Systematic Name English
R-12563 FREE BASE
Code English
dexamisole [INN]
Common Name English
DEXAMISOLE [USAN]
Common Name English
R 12,563 FREE BASE
Code English
IMIDAZO(2,1-B)THIAZOLE, 2,3,5,6-TETRAHYDRO-6-PHENYL-, (R)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C250
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
Code System Code Type Description
SMS_ID
100000083199
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
NCI_THESAURUS
C78042
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
CHEBI
77282
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
238-837-0
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
FDA UNII
UMH46V5U01
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
INN
3571
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
MESH
C028075
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL1369896
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
EVMPD
SUB07020MIG
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
PUBCHEM
66374
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID30163778
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
CAS
14769-74-5
Created by admin on Sat Dec 16 17:55:21 GMT 2023 , Edited by admin on Sat Dec 16 17:55:21 GMT 2023
PRIMARY
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