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  2. 3-Methoxyamphetamine - Wikipedia

    en.wikipedia.org/wiki/3-Methoxyamphetamine

    [1] [13] It produces gepefrine (3-hydroxyamphetamine), a sympathomimetic agent, as one of its major metabolites. [14] 3-MA has appeared on the illicit market as a designer drug alternative to MDMA similarly PMA, although far more rarely than its infamous positional isomer. [15] The 2-aminoindane analogue of 3-MA is 5-methoxy-2-aminoindane (MEAI ...

  3. 3-Methoxymethamphetamine - Wikipedia

    en.wikipedia.org/wiki/3-Methoxymethamphetamine

    3-Methoxymethamphetamine (also known as meta-methoxymethamphetamine or MMMA), which is most closely related to 3-methoxyamphetamine and PMMA and shares similar monoamine releasing effects, although its effects have not been studied so extensively as other related drugs.

  4. Methoxyamphetamine - Wikipedia

    en.wikipedia.org/wiki/Methoxyamphetamine

    Methoxyamphetamine may refer to: 2-Methoxyamphetamine (2-MA) or ortho -methoxyamphetamine (OMA) 3-Methoxyamphetamine (3-MA) or meta -methoxyamphetamine (MMA)

  5. 3-Methoxy-4-methylamphetamine - Wikipedia

    en.wikipedia.org/wiki/3-Methoxy-4-methylamphetamine

    3-Methoxy-4-methylamphetamine (MMA) is an entactogen and psychedelic drug of the phenethylamine and amphetamine classes. [ 1 ] [ 2 ] It was first synthesized in 1970 [ 1 ] and was encountered as a street drug in Italy in the same decade. [ 3 ]

  6. MMDA (drug) - Wikipedia

    en.wikipedia.org/wiki/MMDA_(drug)

    MMDA (3-methoxy-4,5-methylenedioxyamphetamine; 5-methoxy-MDA) is a psychedelic and entactogen drug of the amphetamine class. It is an analogue of lophophine, MDA, and MDMA. MMDA was described by Alexander Shulgin in his book PiHKAL. Shulgin lists the dosage range of MMDA as 100–250 mg.

  7. 4-Hydroxy-3-methoxyamphetamine - Wikipedia

    en.wikipedia.org/wiki/4-Hydroxy-3-methoxyamphetamine

    4-Hydroxy-3-methoxyamphetamine (HMA), also known as 3-O-methyl-α-methyldopamine, is an active metabolite of 3,4-methylenedioxymethamphetamine (MDMA). [ 1 ] [ 2 ] [ 3 ] It is substantially less potent than MDMA or 3,4-methylenedioxyamphetamine (MDA) as a monoamine releasing agent in vitro .

  8. 3,4-Dihydroxymethamphetamine - Wikipedia

    en.wikipedia.org/wiki/3,4-Dihydroxymethamphetamine

    3,4-Dihydroxymethamphetamine (HHMA, 3,4-DHMA), or 3,4-dihydroxy-N-methylamphetamine, also known as α-methylepinine or α,N-dimethyldopamine, is the major metabolite of 3,4-methylenedioxy-N-methylamphetamine (MDMA). [1] [2] [3] It is formed from MDMA by O-demethylation via cytochrome P450 enzymes including CYP2D6 as well as CYP1A2 and CYP3A4.

  9. Trimethoxyamphetamines - Wikipedia

    en.wikipedia.org/wiki/Trimethoxyamphetamines

    Sveriges riksdag added TMA-2 to schedule I ("substances, plant materials and fungi which normally do not have medical use") as narcotics in Sweden as of Dec 30, 1999, published by Medical Products Agency in their regulation LVFS 2004:3 listed as 2,4,5-trimetoxiamfetamin (TMA-2).