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RE104: Synthesis and Activity of a Novel Serotonergic Psychedelic Prodrug of 4-Hydroxy- N , N -diisopropyltryptamine.
- Source :
-
ACS chemical neuroscience [ACS Chem Neurosci] 2024 Jun 19; Vol. 15 (12), pp. 2386-2395. Date of Electronic Publication: 2024 May 17. - Publication Year :
- 2024
-
Abstract
- Results from randomized clinical trials of psilocybin in depressive disorders highlight the therapeutic potential of serotonergic psychedelic compounds in mental health disorders. The synthetic 5-hydroxytryptamine 2A receptor agonist 4-hydroxy- N , N -diisopropyltryptamine (4-OH-DiPT) is structurally similar to psilocin but is reported to have a shorter duration (2-3 h) of psychedelic effects, suggesting the potential for psilocybin-like therapeutic activity with reduced clinical resource burden. Here, we describe the preclinical and translational characterization of RE104, a 4-OH-DiPT prodrug comprising a glutarate moiety designed to cleave rapidly in situ and thus provide reasonable bioavailability of the active drug. Plasma concentration of 4-HO-DiPT over time in PK experiments in rats was correlated with head-twitch intensity. The half-life of 4-OH-DiPT was 40 min after subcutaneous administration of RE104 in rats. In a forced swim test, a single dose of RE104 (1 mg/kg) significantly reduced mean immobility time at 1 week compared with vehicle ( P < 0.001), confirming translational antidepressant potential. Taken together, these data with RE104 show that the glutarate ester can act as an efficient prodrug strategy for 4-HO-DiPT, a unique short-duration psychedelic with potential in depressive disorders.
- Subjects :
- Animals
Male
Rats
Tryptamines pharmacology
Tryptamines chemical synthesis
Tryptamines chemistry
Antidepressive Agents pharmacology
Antidepressive Agents chemical synthesis
Prodrugs pharmacology
Prodrugs chemical synthesis
Hallucinogens pharmacology
Hallucinogens chemical synthesis
Rats, Sprague-Dawley
Subjects
Details
- Language :
- English
- ISSN :
- 1948-7193
- Volume :
- 15
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- ACS chemical neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 38758589
- Full Text :
- https://doi.org/10.1021/acschemneuro.4c00058