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Dimethyltryptamine/harmine

From Wikipedia, the free encyclopedia

Dimethyltryptamine/harmine
Combination of
DimethyltryptamineSerotonergic psychedelic; Serotonin receptor agonist
HarmineReversible inhibitor of monoamine oxidase A
Clinical data
Other namesDMT/harmine; Harmine/dimethyltryptamine; Harmine/DMT; Dimethyltryptamine/telepathine; DMT/telepathine; Telepathine/dimethyltryptamine; telepathine/DMT; RE01
Routes of
administration
Unspecified[1]

Dimethyltryptamine/harmine (developmental code name RE01 or RE-01) is a combination of dimethyltryptamine (DMT), a tryptamine serotonin receptor agonist and serotonergic psychedelic, and harmine, a β-carboline reversible inhibitor of monoamine oxidase A (RIMA), which is under development for the treatment of mood disorders.[1][2][3]

It is a form of pharmahuasca (pharmaceutical ayahuasca), in which DMT is combined with a synthetically produced monoamine oxidase inhibitor (MAOI) as opposed to a plant-derived form such as Banisteriopsis caapi as in ayahuasca.[4] Harmine, acting as a RIMA, inhibits the metabolism of DMT, in turn greatly potentiating DMT and allowing it to become orally active.[5][6][7]

The combination is being developed by Reconnect Labs.[1][2][3] As of August 2023, it is in phase 1 clinical trials.[1][2][3]

See also

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References

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  1. 1 2 3 4 "Dimethyltryptamin/harmine". AdisInsight. 28 August 2023. Retrieved 28 February 2025.
  2. 1 2 3 "Delving into the Latest Updates on Dimethyltryptamine/Telepathine with Synapse". Synapse. 26 January 2025. Retrieved 28 February 2025.
  3. 1 2 3 "Psychedelics Drug Development Tracker". Psychedelic Alpha. Retrieved 28 February 2025.
  4. Brierley DI, Davidson C (December 2012). "Developments in harmine pharmacology--implications for ayahuasca use and drug-dependence treatment". Progress in Neuro-Psychopharmacology & Biological Psychiatry. 39 (2): 263–272. doi:10.1016/j.pnpbp.2012.06.001. PMID 22691716.
  5. Dos Santos RG, Hallak JE (November 2024). "Ayahuasca: pharmacology, safety, and therapeutic effects". CNS Spectrums. 30 (1) e2: 1–9. doi:10.1017/S109285292400213X. PMID 39564645.
  6. Egger K, Aicher HD, Cumming P, Scheidegger M (September 2024). "Neurobiological research on N,N-dimethyltryptamine (DMT) and its potentiation by monoamine oxidase (MAO) inhibition: from ayahuasca to synthetic combinations of DMT and MAO inhibitors". Cellular and Molecular Life Sciences. 81 (1) 395. doi:10.1007/s00018-024-05353-6. PMC 11387584. PMID 39254764.
  7. Berlowitz I, Egger K, Cumming P (2022). "Monoamine Oxidase Inhibition by Plant-Derived β-Carbolines; Implications for the Psychopharmacology of Tobacco and Ayahuasca". Frontiers in Pharmacology. 13 886408. doi:10.3389/fphar.2022.886408. PMC 9121195. PMID 35600851.