ÃÂ-DOM, or psi-DOM, also known as 2,6-dimethoxy-4-methylamphetamine or as Z-7, is a psychedelic drug of the phenethylamine, amphetamine, and è-PEA families related to DOM. It is a positional isomer of DOM in which the methoxy group at the 5 position has been relocated to the 6 position. The drug is taken orally.
In his book PiHKAL (Phenethylamines I Have Known and Loved), Alexander Shulgin lists ÃÂ-DOM's dose as 15 to 25mg orally and its duration as 6 to 8hours. The effects of ÃÂ-DOM were reported to include feeling weird or strange, closed-eye imagery, some visuals, introspection, feeling stoned, spaciness, lightheadedness, muscle tremors, palpitations, and diarrhea. The visuals were said to have been less than expected based on the intensity of its effects. The drug is about one-third as potent as DOM.
ÃÂ-DOM shows affinity for the serotonin 5-HT<sub>2A</sub> and 5-HT<sub>2C</sub> receptors (K<sub>i</sub> = 49âÂÂ351nM and 50nM, respectively). Its affinity for the serotonin 5-HT<sub>2A</sub> receptor was about 2.6- to 3.5-fold lower than that of DOM. The drug acts as an agonist of the serotonin 5-HT<sub>2A</sub> receptor similarly to DOM.
ÃÂ-DOM has been found to substitute for LSD and 5-MeO-DMT in rodent drug discrimination tests. Conversely, it did not substitute for the serotonin 5-HT<sub>1A</sub> receptor agonist LY-293284 in such tests.
The chemical synthesis of ÃÂ-DOM has been described.
Analogues of ÃÂ-DOM include other ÃÂ-PEA derivatives like TMA-6 (ÃÂ-TMA-2), è-2C-T-4, and è-DODFMO, among others.
è-DOM was first described in the literature by Alexander Shulgin in 1970. Subsequently, it was described in greater detail by Shulgin in his 1991 book PiHKAL (Phenethylamines I have Known and Loved).
è-DOM is a controlled substance in Canada under phenethylamine blanket-ban language.
è-DOM is not an explicitly controlled substance in the United States. However, it could be considered a controlled substance under the Federal Analogue Act if intended for human consumption. In addition, it may be considered scheduled as a positional isomer of DOM.