Potential Functional Role of Phenethylamine Derivatives in Inhibiting Dopamine Reuptake: Structure-Activity Relationship.
Docking simulation
Dopamine D
Dopamine transporter
Drug addiction
Phenethylamine
Structure activity relationship
Journal
Biomolecules & therapeutics
ISSN: 1976-9148
Titre abrégé: Biomol Ther (Seoul)
Pays: Korea (South)
ID NLM: 101472832
Informations de publication
Date de publication:
01 Jan 2023
01 Jan 2023
Historique:
received:
10
04
2022
revised:
25
07
2022
accepted:
03
08
2022
pubmed:
14
9
2022
medline:
14
9
2022
entrez:
13
9
2022
Statut:
ppublish
Résumé
Numerous psychotropic and addictive substances possess structural features similar to those of β-phenethylamine (β-PEA). In this study, we selected 29 β-PEA derivatives and determined their structure-activity relationship (SAR) to their ability to inhibit dopamine (DA) reuptake; conducted docking simulation for two selected compounds; and identified their potential functionals. The compounds were subdivided into arylethylamines, 2-(alkyl amino)-1-arylalkan-1-one derivatives and alkyl 2-phenyl-2-(piperidin-2-yl)acetate derivatives. An aromatic group, alkyl group, and alkylamine derivative were attached to the arylethylamine and 2-(alkyl amino)-1-arylalkan-1-one derivatives. The inhibitory effect of the compounds on dopamine reuptake increased in the order of the compounds substituted with phenyl, thiophenyl, and substituted phenyl groups in the aromatic position; compounds with longer alkyl groups and smaller ring-sized compounds at the alkylamine position showed stronger inhibitory activities. Docking simulation conducted for two compounds,
Identifiants
pubmed: 36098044
pii: biomolther.2022.047
doi: 10.4062/biomolther.2022.047
pmc: PMC9810443
doi:
Types de publication
Journal Article
Langues
eng
Pagination
108-115Références
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