Computational design of an improved photoswitchable psychedelic based on light absorption, membrane permeation and protein binding.

ABSTRACT: Psychedelic compounds can induce rapid-acting and long-lasting antidepressant benefits. Understanding the role of their hallucinatory effects is crucial for shaping the future trajectory of antidepressant drug development. Photoswitchable compounds targeting the 5-HT_2AR offer precise spatio-temporal control over the activation of different downstream pathways. In this work, we computationally discovered PQ-azo-N,N-DMT (34), a photoswitch with improved features compared to the previously synthesized azo-N,N-DMT (1). The new compound shows tight binding to the 5-HT_2AR, retaining all important interactions of lysergic acid diethylamide (LSD), exhibits positive membrane permeability, and has a strong red-shifted absorption that would allow phot

SUBMITTER: Palmisano VF 

PROVIDER: S-EPMC12396349 | biostudies-literature | 2025 Sep

REPOSITORIES: biostudies-literature