Details
Stereochemistry | RACEMIC |
Molecular Formula | C11H15N.ClH |
Molecular Weight | 197.704 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.NC(CC=C)CC1=CC=CC=C1
InChI
InChIKey=SSUPWSZOVWZDRV-UHFFFAOYSA-N
InChI=1S/C11H15N.ClH/c1-2-6-11(12)9-10-7-4-3-5-8-10;/h2-5,7-8,11H,1,6,9,12H2;1H
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 | ( + / - ) |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
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
Fri Dec 15 16:13:47 GMT 2023
by
admin
on
Fri Dec 15 16:13:47 GMT 2023
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Record UNII |
8R38M8PU9W
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Record Status |
Validated (UNII)
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Record Version |
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-
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Code | English | ||
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Code | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C265
Created by
admin on Fri Dec 15 16:13:47 GMT 2023 , Edited by admin on Fri Dec 15 16:13:47 GMT 2023
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NCI_THESAURUS |
C241
Created by
admin on Fri Dec 15 16:13:47 GMT 2023 , Edited by admin on Fri Dec 15 16:13:47 GMT 2023
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Code System | Code | Type | Description | ||
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4255-24-7
Created by
admin on Fri Dec 15 16:13:47 GMT 2023 , Edited by admin on Fri Dec 15 16:13:47 GMT 2023
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PRIMARY | |||
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20253
Created by
admin on Fri Dec 15 16:13:47 GMT 2023 , Edited by admin on Fri Dec 15 16:13:47 GMT 2023
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PRIMARY | |||
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8R38M8PU9W
Created by
admin on Fri Dec 15 16:13:47 GMT 2023 , Edited by admin on Fri Dec 15 16:13:47 GMT 2023
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PRIMARY | |||
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169879
Created by
admin on Fri Dec 15 16:13:47 GMT 2023 , Edited by admin on Fri Dec 15 16:13:47 GMT 2023
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PRIMARY | |||
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CHEMBL2110598
Created by
admin on Fri Dec 15 16:13:47 GMT 2023 , Edited by admin on Fri Dec 15 16:13:47 GMT 2023
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PRIMARY | |||
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C100050
Created by
admin on Fri Dec 15 16:13:47 GMT 2023 , Edited by admin on Fri Dec 15 16:13:47 GMT 2023
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PRIMARY | |||
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C80252
Created by
admin on Fri Dec 15 16:13:47 GMT 2023 , Edited by admin on Fri Dec 15 16:13:47 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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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |