| Autor: |
M. Ro?rsted, Emil, Jensen, Anders A., Smits, Gints, Frydenvang, Karla, Kristensen, Jesper L. |
| Zdroj: |
Journal of Medicinal Chemistry; May 2024, Vol. 67 Issue: 9 p7224-7244, 21p |
| Abstrakt: |
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. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
|
