Revision as of 00:46, 8 May 2017 editAlyInWikiWonderland (talk | contribs)Autopatrolled, Extended confirmed users81,666 editsNo edit summary← Previous edit | Revision as of 14:38, 17 June 2018 edit undo98.116.227.17 (talk) If this compound is a dopamine and serotonin releasing agent, then those are desirable psychoactive properties. Amphetamine itself is desirable for being a dopamine releasing agent (DRA), and serotonin releasing agents are desirable as well (though possibly lacking of the self-reinforcing properties of DRAs). Desirable is also a loosely defined term, though this compound would seem to be desirable for therapeutic, productivity-enhancing, and recreational usage.Next edit → | ||
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More than a dozen deaths have been reported throughout Europe in 2012-2013 after consumption of amphetamine ('speed') contaminated with 4-methylamphetamine. | More than a dozen deaths have been reported throughout Europe in 2012-2013 after consumption of amphetamine ('speed') contaminated with 4-methylamphetamine. | ||
A contaminated precursor, after synthesis yielding a mixture of amphetamine and 4-MA, seems the logical culprit.<ref>{{Cite journal|title = 4-Methyl-amphetamine: a health threat for recreational amphetamine users|journal = Journal of Psychopharmacology |date = 2013-09-01|issn = 1461-7285|pmid = 23784740|pages = 817–822|volume = 27|issue = 9|doi = 10.1177/0269881113487950|first = P.|last = Blanckaert|first2 = Jgc|last2 = van Amsterdam|first3 = Tm|last3 = Brunt|first4 = Jdj|last4 = van den Berg|first5 = F.|last5 = Van Durme|first6 = K.|last6 = Maudens|first7 = Jch|last7 = van Bussel}}</ref> | |||
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Revision as of 14:38, 17 June 2018
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Routes of administration | Oral, intranasal, injection |
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Elimination half-life | 6-12 hours |
Excretion | Urine |
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Formula | C10H15N |
Molar mass | 149.23 g/mol g·mol |
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4-Methylamphetamine (4-MA; PAL-313; Aptrol; p-TAP) is a stimulant and anorectic drug of the phenethylamine and amphetamine chemical classes.
In vitro, it acts as a potent and balanced serotonin, norepinephrine, and dopamine releasing agent with Ki affinity values of 53.4nM, 22.2nM, and 44.1nM at the serotonin, norepinephrine, and dopamine transporters, respectively. However, more recent in vivo studies that involved performing microdialysis on rats showed a different trend. These studies showed that 4-methylamphetamine is much more potent at elevating serotonin (~18 x baseline) relative to dopamine (~5 x baseline). The authors speculated that this is because 5-HT release dampens DA release through some mechanism. For example, it was suggested that a possible cause for this could be activation of 5HT2C receptors since this is known to inhibit DA release. In addition there are alternative explanations such as 5-HT release then going on to encourage GABA release, which has an inhibitory effect on DA neurons.
4-MA was investigated as an appetite suppressant in 1952 and was even given a trade name, Aptrol, but development was apparently never completed. More recently it has been reported as a novel designer drug.
In animal studies, 4-MA was shown to have the lowest rate of self-administration out of a range of similar drugs tested (the others being 3-methylamphetamine, 4-fluoroamphetamine, and 3-fluoroamphetamine), likely as a result of having the highest potency for releasing serotonin relative to dopamine.
More than a dozen deaths have been reported throughout Europe in 2012-2013 after consumption of amphetamine ('speed') contaminated with 4-methylamphetamine.
A contaminated precursor, after synthesis yielding a mixture of amphetamine and 4-MA, seems the logical culprit.
- 1-(4-Methylphenyl)-2-aminobutane
- 2-Methylamphetamine
- 3-Methylamphetamine
- 4-Methyl-N-methylamphetamine
- 4-Methyl-N-methylcathinone
- 3-Methoxy-4-methylamphetamine
- 3,4-Dimethylamphetamine
References
- Wee, S.; Anderson, KG; Baumann, MH; Rothman, RB; Blough, BE; Woolverton, WL (2004). "Relationship between the Serotonergic Activity and Reinforcing Effects of a Series of Amphetamine Analogs". Journal of Pharmacology and Experimental Therapeutics. 313 (2): 848–854. doi:10.1124/jpet.104.080101. PMID 15677348.
- Di Giovanni, Giuseppe; Esposito, Ennio; Di Matteo, Vincenzo (2010). "Role of Serotonin in Central Dopamine Dysfunction". CNS Neuroscience & Therapeutics. 16 (3): 179–194. doi:10.1111/j.1755-5949.2010.00135.x. PMID 20557570.
- Gelvin, EP; McGavack, TH (1952). "2-Amino-1-(p-methylphenyl)-propane (aptrol) as an anorexigenic agent in weight reduction". New York State Journal of Medicine. 52 (2): 223–6. PMID 14890975.
- Wee, S; Anderson, KG; Baumann, MH; Rothman, RB; Blough, BE; Woolverton, WL (2005). "Relationship between the serotonergic activity and reinforcing effects of a series of amphetamine analogs". The Journal of Pharmacology and Experimental Therapeutics. 313 (2): 848–54. doi:10.1124/jpet.104.080101. PMID 15677348.
- Baumann, MH; Clark, RD; Woolverton, WL; Wee, S; Blough, BE; Rothman, RB. (Apr 2011). "In vivo effects of amphetamine analogs reveal evidence for serotonergic inhibition of mesolimbic dopamine transmission in the rat". Journal of Pharmacology and Experimental Therapeutics. 337 (1): 218–25. doi:10.1124/jpet.110.176271. PMC 3063744. PMID 21228061.
- Blanckaert, P.; van Amsterdam, Jgc; Brunt, Tm; van den Berg, Jdj; Van Durme, F.; Maudens, K.; van Bussel, Jch (2013-09-01). "4-Methyl-amphetamine: a health threat for recreational amphetamine users". Journal of Psychopharmacology. 27 (9): 817–822. doi:10.1177/0269881113487950. ISSN 1461-7285. PMID 23784740.
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DRAsTooltip Dopamine releasing agents |
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NRAsTooltip Norepinephrine releasing agents |
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SRAsTooltip Serotonin releasing agents |
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See also: Receptor/signaling modulators • Monoamine reuptake inhibitors • Adrenergics • Dopaminergics • Serotonergics • Monoamine metabolism modulators • Monoamine neurotoxins |
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Phenethylamines |
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Amphetamines |
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Cathinones |
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Phenylalkylpyrrolidines | |
Catecholamines (and close relatives) |
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Miscellaneous |
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