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Other names | 4-HT; 4-HTA; N,N-Didesmethylpsilocin; Dinorpsilocin |
Drug class | Serotonin receptor agonist; Non-hallucinogenic serotonin 5-HT2A receptor agonist |
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Chemical and physical data | |
Formula | C10H12N2O |
Molar mass | 176.219 g·mol−1 |
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4-Hydroxytryptamine (4-HT, 4-HTA), also known as N,N-didesmethylpsilocin, is a naturally occurring tryptamine alkaloid.[1][2][3] It is a positional isomer of serotonin (5-hydroxytryptamine; 5-HT) and is the dephosphorylated form of norbaeocystin.[4] The compound may serve as an alternative precursor of psilocybin in psilocybin mushrooms.[1][5][2]
4-HT is a potent agonist of the serotonin 5-HT2A receptor similarly to psilocin.[3] It is centrally penetrant.[3] Surprisingly however, the compound, similarly to baeocystin, norbaeocystin, and norpsilocin, does not produce the head-twitch response, a behavioral proxy of psychedelic effects, in animals, and hence is putatively non-hallucinogenic.[3][6] In older literature, the psychoactive effects of 4-hydroxylated tryptamines have been said to increase in the series of 4-hydroxytryptamine, 4-hydroxy-N-methyltryptamine (norpsilocin), and 4-hydroxy-N,N-dimethyltryptamine (psilocin).[2] The reason for the lack of hallucinogenic effects with 4-HT and related compounds is unknown, but may be due to biased agonism of the serotonin 5-HT2A receptor; or, more specifically, biased agonism for the β-arrestin2 signaling pathway.[3]
Norbaeocystin is thought to be a prodrug of 4-HT, analogously to how psilocybin is a prodrug of psilocin and how baeocystin is thought to be a prodrug of norpsilocin.[7][3]
4-Hydroxytryptamine was first described in the scientific literature by 1959.[8][9] Its pharmacology was first thoroughly characterized in 2024.[3]