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  2. Amphetamine type stimulant - Wikipedia

    en.wikipedia.org/wiki/Amphetamine_type_stimulant

    Amphetamine type stimulants can be used in the treatment of narcolepsy, a rare neurological disorder where the brain is unable to regulate the sleep-wake mechanism. [17] Amphetamines causes an increase in dopamine release, which is the proposed mechanism for its wake-promoting effect. [18]

  3. 3-Methylamphetamine - Wikipedia

    en.wikipedia.org/wiki/3-Methylamphetamine

    3-Methylamphetamine (3-MeA; PAL-314) is a stimulant drug from the amphetamine family. It is self-administered by mice to a similar extent to 4-fluoroamphetamine and has comparable properties as a monoamine releaser, [1] although with a more balanced release of all three monoamines, as opposed to the more dopamine/noradrenaline selective fluoro analogues.

  4. Methamphetamine - Wikipedia

    en.wikipedia.org/wiki/Methamphetamine

    [25] [144] When taken orally, 30–54% of the dose is excreted in urine as methamphetamine and 10–23% as amphetamine. [144] Following IV doses, about 45% is excreted as methamphetamine and 7% as amphetamine. [144] The elimination half-life of methamphetamine varies with a range of 5–30 hours, but it is on average 9 to 12 hours in most studies.

  5. Amphetamine - Wikipedia

    en.wikipedia.org/wiki/Amphetamine

    The adverse side effects of amphetamine are many and varied, and the amount of amphetamine used is the primary factor in determining the likelihood and severity of adverse effects. [29] [41] Amphetamine products such as Adderall, Dexedrine, and their generic equivalents are currently approved by the U.S. FDA for long-term therapeutic use.

  6. Dimethylamphetamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylamphetamine

    Dimethylamphetamine has weaker stimulant effects than amphetamine or methamphetamine and is considerably less addictive [1] and less neurotoxic compared to methamphetamine. [ 2 ] [ 3 ] However, it still retains some mild stimulant effects and abuse potential, [ 4 ] and is a Schedule I controlled drug.

  7. 3,4-Methylenedioxyamphetamine - Wikipedia

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

    MDA is a substituted methylenedioxylated phenethylamine and amphetamine derivative. In relation to other phenethylamines and amphetamines, it is the 3,4-methylenedioxy, α-methyl derivative of β-phenylethylamine, the 3,4-methylenedioxy derivative of amphetamine, and the N-desmethyl derivative of MDMA.

  8. 3,4-Methylenedioxy-N-ethylamphetamine - Wikipedia

    en.wikipedia.org/wiki/3,4-methylenedioxy-N-ethyl...

    MDEA is a substituted amphetamine and a substituted methylenedioxyphenethylamine. MDEA acts as a serotonin, norepinephrine, and dopamine releasing agent and reuptake inhibitor. [1] Possession of MDEA is illegal in most countries. Some limited exceptions exist for scientific and medical research.

  9. 3-Methoxyamphetamine - Wikipedia

    en.wikipedia.org/wiki/3-Methoxyamphetamine

    meta-Methoxyamphetamine [1] (MMA), also known as 3-methoxyamphetamine (3-MA), is a stimulant drug from the amphetamine family. It has similar effects in animal drug discrimination tests to the more widely known derivative 4-methoxyamphetamine (PMA), [2] although with a slightly different ratio of monoamine release, being a combined serotonin, dopamine, and norepinephrine releasing agent rather ...