Drug intelligence / Profile preview

psilocin mucate

Development stage
Phase 1
Lead developer
Lobe Sciences
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules
Administration
Oral
01

Overview

Psilocin mucate is a novel, stabilized salt form of psilocin, the active metabolite of the psychedelic prodrug psilocybin. Developed to address the instability and poor bioavailability of free psilocin, this compound is formed by combining psilocin with mucic acid. Unlike psilocybin, which requires enzymatic conversion in the body to become active, psilocin mucate dissociates rapidly in the gastrointestinal tract to release free psilocin for absorption. This results in rapid onset and highly reproducible pharmacokinetics with 100% bioavailability reported in Phase 1 studies. Notably, clinical data indicate that at therapeutic doses (e.g., 4 mg), it produces anti-anxiolytic effects without hallucinogenic side effects and demonstrates a favorable safety profile. The drug is being developed primarily for neurological disorders such as chronic cluster headache but may have broader applications due to its stable oral formulation and superior pharmacokinetic properties compared to both free psilocin and its prodrug, psilocybin[1][2][5][8][9].

Brand names
Conjugated Psilocin
Other names
psilocin mucateL-130L130L 130Conjugated Psilocin
02

Targets

HTR1A (Serotonin receptor 1A (5-hydroxytryptamine receptor 1A))HTR2A (Serotonin receptor 5-HT2A)

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