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Dimethyltryptamine/harmine

From Wikipedia, the free encyclopedia

Not to be confused withDimethyltryptamine/β-carbolines.
Pharmaceutical compound
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 nameRE01 orRE-01) is acombination ofdimethyltryptamine (DMT), atryptamineserotonin receptor agonist andserotonergic psychedelic, andharmine, aβ-carbolinereversible inhibitor of monoamine oxidase A (RIMA), which is under development for the treatment ofmood disorders.[1][2][3]

It is a form ofpharmahuasca (pharmaceutical ayahuasca), in which DMT is combined with asynthetically producedmonoamine oxidase inhibitor (MAOI) as opposed to aplant-derived form such asBanisteriopsis caapi as inayahuasca.[4] Harmine, acting as a RIMA, inhibits themetabolism of DMT, in turn greatly potentiating DMT and allowing it to becomeorally active.[5][6][7]

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

See also

[edit]

References

[edit]
  1. ^abcd"Dimethyltryptamin/harmine".AdisInsight. 28 August 2023. Retrieved28 February 2025.
  2. ^abc"Delving into the Latest Updates on Dimethyltryptamine/Telepathine with Synapse".Synapse. 26 January 2025. Retrieved28 February 2025.
  3. ^abc"Psychedelics Drug Development Tracker".Psychedelic Alpha. Retrieved28 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.
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AAADTooltip Aromatic L-amino acid decarboxylase
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