Luvesilocin
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| Other names | RE-104; RE104; FT-104; FT104; 4-Glutaryloxy-N,N-diisopropyltryptamine; 4-Hydroxy-N,N-diisopropyltryptamine O-glutarate; O-Glutaryl-4-hydroxy-N,N-diisopropyltryptamine; 4-HO-DiPT glutarate; O-Glutaryl-4-HO-DiPT; 4-GO-DiPT |
| Routes of administration | Oral, subcutaneous injection |
| Drug class | Non-selective serotonin receptor agonist; Serotonin 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen |
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| Pharmacokinetic data | |
| Metabolites | • 4-HO-DiPT |
| Onset of action | ≤1 hour (s.c.) |
| Elimination half-life | • Luvesilocin: 0.43–0.64 hours (s.c.) • 4-HO-DiPT: 2.7–4.1 hours (s.c.) |
| Duration of action | 3.6 hours (range ~3–4 hours) (s.c.) |
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| Chemical and physical data | |
| Formula | C21H30N2O |
| Molar mass | 326.484 g·mol−1 |
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Luvesilocin, also known as RE104 and FT-104, as well as 4-glutaryloxy-N,N-diisopropyltryptamine (4-HO-DiPT O-glutarate or 4-GO-DiPT), is a psychedelic drug of the tryptamine and 4-hydroxytryptamine families which is under development for the treatment of psychiatric disorders. It is taken orally or by subcutaneous injection.
The drug is a prodrug ester of 4-HO-DiPT, which acts as a non-selective serotonin receptor agonist including of the serotonin 5-HT2A receptor.
Luvesilocin was first described in the literature in 2021. It is under development for the treatment of postpartum depression and treatment-resistant depression. As of September 2025, the drug has reached phase 2 clinical trials. A phase 3 trial is planned for 2026.