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J Med Chem ; 67(9): 7224-7244, 2024 May 09.
Artículo en Inglés | MEDLINE | ID: mdl-38648420

RESUMEN

Classical psychedelics such as psilocybin, lysergic acid diethylamide (LSD), and N,N-dimethyltryptamine (DMT) are showing promising results in clinical trials for a range of psychiatric indications, including depression, anxiety, and substance abuse disorder. These compounds are characterized by broad pharmacological activity profiles, and while the acute mind-altering effects can be ascribed to their shared agonist activity at the serotonin 2A receptor (5-HT2AR), their apparent persistent therapeutic effects are yet to be decidedly linked to activity at this receptor. We report herein the discovery of 2,5-dimethoxyphenylpiperidines as a novel class of selective 5-HT2AR agonists and detail the structure-activity investigations leading to the identification of LPH-5 [analogue (S)-11] as a selective 5-HT2AR agonist with desirable drug-like properties.


Asunto(s)
Piperidinas , Receptor de Serotonina 5-HT2A , Agonistas del Receptor de Serotonina 5-HT2 , Animales , Humanos , Ratas , Descubrimiento de Drogas , Piperidinas/farmacología , Piperidinas/química , Piperidinas/síntesis química , Receptor de Serotonina 5-HT2A/metabolismo , Agonistas del Receptor de Serotonina 5-HT2/farmacología , Agonistas del Receptor de Serotonina 5-HT2/química , Agonistas del Receptor de Serotonina 5-HT2/síntesis química , Relación Estructura-Actividad , Dietilamida del Ácido Lisérgico/síntesis química , Dietilamida del Ácido Lisérgico/química , Dietilamida del Ácido Lisérgico/farmacología
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