Details
Stereochemistry | RACEMIC |
Molecular Formula | C11H15N |
Molecular Weight | 161.2435 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(CC=C)CC1=CC=CC=C1
InChI
InChIKey=WQKXQJYCZMWOSD-UHFFFAOYSA-N
InChI=1S/C11H15N/c1-2-6-11(12)9-10-7-4-3-5-8-10/h2-5,7-8,11H,1,6,9,12H2
Molecular Formula | C11H15N |
Molecular Weight | 161.2435 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
ALFETAMINE (aletamine) is an antidepressant and analgesic. The pharmacologic activity profile of aletamine closely resembles that of the tricyclic antidepressants imipramine and amitriptyline. Effects shared are antagonism of RO4-1284-induced ptosis and depressed exploratory behavior, depression of spontaneous motor activity, prolongation of hexobarbital hypnosis and anticonvulsant action in mice, hypotension and potentiation of norepinephrine pressor effects in dogs, antimuricidal effects, hypothermia in rats and local anesthesia in rabbits and guinea pigs. Aletamine differed from imipramine and amitriptyline as follows: (1) aletamine exerted no apparent central or peripheral anticholinergic effect as suggested by lack of influence on tremorine-induced tremors or salivation; (2) although aletamine was less potent on a milligram basis than imipramine and amitriptyline in preventing RO4-1284 depression, aletamine was more potent than imipramine in counteracting existing reserpine depression (ptosis, depressed exploratory behavior) in mice. Amitriptyline was inactive against reserpine depression. The pharmacologic effects of aletamine differ in several respects from those of d-amphetamine. The effects of aletamine on spontaneous motor activity, hexobarbital hypnosis and body temperature in rodents and on blood pressure in dogs are in opposite direction to those of amphetamine. In further contrast to amphetamine, grouping of mice has no influence on the toxicity of aletamine. Aletamine does not appear to be an inhibitor of monoamine oxidase in vivo since it does not enhance tryptamine-induced convulsions in rats.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:05:24 GMT 2023
by
admin
on
Sat Dec 16 16:05:24 GMT 2023
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Record UNII |
Q3V87119BP
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C265
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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NCI_THESAURUS |
C241
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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Code System | Code | Type | Description | ||
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SUB05318MIG
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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100000087876
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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Q3V87119BP
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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CHEMBL2110598
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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C78005
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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20254
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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4255-23-6
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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DTXSID60863350
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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1931
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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ALFETAMINE
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY | |||
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C100050
Created by
admin on Sat Dec 16 16:05:25 GMT 2023 , Edited by admin on Sat Dec 16 16:05:25 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |