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Ψ-PEA (psychedelics)

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Ψ-PEA (psychedelics)
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Ψ-Phenethylamines (Ψ-PEA), or psi-phenethylamines (psi-PEA), also known as 4-substituted 2,6-dimethoxyphenethylamines, are a family of psychedelic and related compounds of the phenethylamine family.[1][2][3] They are positional isomers of the 4-substituted 2,5-dimethoxyphenethylamines (e.g., 2Cs and DOx) and 4-substituted 3,5-dimethoxyphenethylamines (e.g., scalines and 3Cs).[1][2][3]

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TMA-6 (Ψ-TMA-2) is an example of a Ψ-PEA psychedelic.[1][2][3]

Like the preceding groups or substitution patterns of phenethylamine psychedelics, many Ψ-PEA derivatives are likewise potent serotonergic psychedelics and are known to act as serotonin 5-HT2A receptor agonists.[4][1][2][3] Examples of known psychedelic Ψ-PEAs include TMA-6 (Ψ-TMA-2) and Ψ-DOM, Ψ-2C-T-4, Ψ-2C-DFMO, and Ψ-DODFMO.[4][1][2][3] Conversely, Ψ-2C-O (TMPEA-6) was inactive.[1][4] Unlike many other psychedelic phenethylamines, Ψ-PEAs such as TMA-6, Ψ-Aleph, and Ψ-Aleph-2 are known to act as potent monoamine oxidase inhibitors (MAOIs).[1][5]

The Ψ-PEAs are relatively unexplored compared to the other major psychedelic phenethylamine groups.[1][2][3][6][7][8][9] Many Ψ-PEAs have been synthesized or described, but few are known to have been tested in humans.[1]

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List and properties of Ψ-PEAs

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See also

References

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