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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
Structure of ALFETAMINE HYDROCHLORIDE

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

HIDE SMILES / InChI

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

PubMed

PubMed

TitleDatePubMed
Analgesic activity profile of alpha-allylphenethylamine HCl (aletamine).
1968-04
Aletamine in hospitalized schizophrenic patients--negative report.
1967-03-01
Clinical evaluation of aletamine as an analgesic.
1966-03-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:22:31 GMT 2025
Edited
by admin
on Mon Mar 31 18:22:31 GMT 2025
Record UNII
8R38M8PU9W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALETAMINE HYDROCHLORIDE
USAN  
USAN  
Preferred Name English
ALFETAMINE HYDROCHLORIDE
Common Name English
ALETAMINE HYDROCHLORIDE [USAN]
Common Name English
BENZENEETHANAMINE, .ALPHA.-2-PROPENYL-, HYDROCHLORIDE
Systematic Name English
?-Allylphenethylamine hydrochloride
Systematic Name English
ALETAMINE HCL
Common Name English
NDR-5061A
Code English
NSC-169879
Code English
Classification Tree Code System Code
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
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
Code System Code Type Description
CAS
4255-24-7
Created by admin on Mon Mar 31 18:22:31 GMT 2025 , Edited by admin on Mon Mar 31 18:22:31 GMT 2025
PRIMARY
PUBCHEM
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
PRIMARY
FDA UNII
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
PRIMARY
SMS_ID
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
PRIMARY
NSC
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
PRIMARY
ChEMBL
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
PRIMARY
MESH
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
PRIMARY
EPA CompTox
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
PRIMARY
NCI_THESAURUS
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
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY