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
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
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
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:55:21 GMT 2023
by
admin
on
Sat Dec 16 17:55:21 GMT 2023
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Record UNII |
UMH46V5U01
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C250
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100000083199
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C78042
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77282
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238-837-0
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UMH46V5U01
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3571
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C028075
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CHEMBL1369896
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SUB07020MIG
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66374
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DTXSID30163778
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14769-74-5
Created by
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PRIMARY |
Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
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ACTIVE MOIETY |