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  2. Dexamyl - Wikipedia

    en.wikipedia.org/wiki/Dexamyl

    Its name is a portmanteau of dextro- amphetamine and amyl- barbitone. [ citation needed ] Dexamyl was discontinued in 1982 by SKF in favor of monoamine oxidase inhibitors (MAOIs) and tricyclic antidepressants (TCAs) which were recently developed and shared treatment indications with Dexamyl yet lacked the high dependence potential and abuse ...

  3. File:GLAM tool.pdf - Wikipedia

    en.wikipedia.org/wiki/File:GLAM_tool.pdf

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  4. History and culture of substituted amphetamines - Wikipedia

    en.wikipedia.org/wiki/History_and_culture_of...

    [4] [9] During the Persian Gulf War, amphetamine became the drug of choice for American bomber pilots, being used voluntarily by roughly half of U.S. Air Force pilots. [48] The Tarnak Farm incident during the War in Afghanistan (2001-21) , in which an American F-16 pilot killed several friendly Canadian soldiers on the ground, was blamed by the ...

  5. Category:Substituted amphetamines - Wikipedia

    en.wikipedia.org/wiki/Category:Substituted...

    It should only contain pages that are about a substituted amphetamine or lists of substituted amphetamines, as well as subcategories containing those things (themselves set categories). Topics about substituted amphetamines in general should be placed in relevant topic categories .

  6. 2,5-Dimethoxy-4-chloroamphetamine - Wikipedia

    en.wikipedia.org/wiki/2,5-Dimethoxy-4-chloro...

    A normal average dose of DOC ranges from 0.2–7.0 mg [19] the former producing threshold effects, and the latter producing extremely strong effects. Onset of the drug is 1–3 hours, peak and plateau at 4–8 hours, and a gradual come down with residual stimulation at 9-20h.

  7. Propylamphetamine - Wikipedia

    en.wikipedia.org/wiki/Propylamphetamine

    It was first developed in the 1970s, mainly for research into the metabolism of, [1] and as a comparison tool to, other amphetamines. [ 2 ] Propylamphetamine is inactive as a dopamine releasing agent in vitro and instead acts as a low- potency dopamine reuptake inhibitor with an IC 50 Tooltip half-maximal inhibitory concentration of 1,013 nM. [ 3 ]

  8. Methoxyphenamine - Wikipedia

    en.wikipedia.org/wiki/Methoxyphenamine

    Methoxyphenamine (trade names ASMI, Euspirol, Orthoxine, Ortodrinex, Proasma), also known as 2-methoxy-N-methyl amphetamine (OMMA), is a β-adrenergic receptor agonist of the amphetamine class used as a bronchodilator.

  9. 2,5-Dimethoxy-4-bromoamphetamine - Wikipedia

    en.wikipedia.org/wiki/2,5-Dimethoxy-4-bromo...

    Omission of the amphetamine related α-methyl leads to 2C-B, a compound that possesses a lower affinity for the 5-HT2A receptor and is a weaker receptor agonist which results in drastically reduced vasoconstriction. [citation needed]