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
Mon Mar 31 18:22:31 GMT 2025
by
admin
on
Mon Mar 31 18:22:31 GMT 2025
|
| Record UNII |
8R38M8PU9W
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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Preferred Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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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 Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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NCI_THESAURUS |
C241
Created by
admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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4255-24-7
Created by
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PRIMARY | |||
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20253
Created by
admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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PRIMARY | |||
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8R38M8PU9W
Created by
admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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PRIMARY | |||
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300000055030
Created by
admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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PRIMARY | |||
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169879
Created by
admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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PRIMARY | |||
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CHEMBL2110598
Created by
admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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PRIMARY | |||
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C100050
Created by
admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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PRIMARY | |||
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DTXSID801350458
Created by
admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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PRIMARY | |||
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C80252
Created by
admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE | |||
|
|
PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
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ACTIVE MOIETY |