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6-Fluoro-AMT

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(Redirected from6-Fluoro-αMT)
Chemical compound
Pharmaceutical compound
6-Fluoro-AMT
Clinical data
Other names6-Fluoro-AMT; 6-Fluoro-αMT; 6F-AMT; 6F-αMT; 6-F-AMT; 6-F-αMT; 6-Fluoro-α-methyltryptamine
Drug classSerotonergic psychedelic;Hallucinogen
Identifiers
  • 1-(6-fluoro-1H-indol-3-yl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H13FN2
Molar mass192.237 g·mol−1
3D model (JSmol)
  • NC(C)CC1=CNC2=CC(F)=CC=C21
  • InChI=1S/C11H13FN2/c1-7(13)4-8-6-14-11-5-9(12)2-3-10(8)11/h2-3,5-7,14H,4,13H2,1H3
  • Key:XYJYWUUXCUJXAI-UHFFFAOYSA-N

6-Fluoro-AMT, or6-fluoro-αMT, also known as6-fluoro-α-methyltryptamine, is apsychedelic drug of thetryptamine family related toα-methyltryptamine (AMT) and5-MeO-AMT.[1][2]

Use and effects

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6-Fluoro-AMT was allegedly manufactured and sold from the laboratory operated byLeonard Pickard andGordon Todd Skinner, who described 6-fluoro-AMT as "a beast".[1] In interviews, Skinner stated that he first began to experiment with 6-fluoro-AMT in the early 1980s by giving it to high school friends.[2] Their experiences made him cautious about the appropriate doses, which he said ranged from 25 to 75 mg (Skinner weighed about 250 lbs at the time of his own bioassay).[2] Skinner said that 6-fluoro-AMT is a long-lasting psychedelic with more time distortion and that it was enhanced by combination withALD-52.[2]

Interactions

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Pharmacology

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Pharmacodynamics

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Animal tests showed the drug to be somewhat lesspotent in terms ofpharmacological activity than AMT or5-fluoro-AMT.[3] It produces thehead-twitch response, a behavioral proxy ofpsychedelic-like effects, in rodents.[4][5][6] ItsIC50Tooltip half-maximal inhibitory concentration formonoamine oxidase A (MAO-A)inhibition is 580 to 1,800 nM, compared to 180 to 450 nM for5-fluoro-AMT and 380 nM for AMT.[5][7][8]

Chemistry

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Analogues

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Analogues of 6-fluoro-AMT includeα-methyltryptamine (AMT),5-fluoro-AMT,5-chloro-AMT,5-fluoro-AET,5-chloro-AET,6-fluoro-DMT,6-fluoro-DET,7-chloro-AMT, andO-4310 (1-isopropyl-6-fluoro-4-HO-DMT), among others.

History

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6-Fluoro-AMT was first described in thescientific literature, by Asher Kalir andStephen Szara, by at least 1963.[3]

See also

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References

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  1. ^abMorris H (2010)."Life is a Cosmic Giggle on the Breath of the Universe. A Tour of Gordon Todd Skinner's Subterranean LSD Palace".Vice Magazine.Archived from the original on 2014-10-13. Retrieved2017-08-23.
  2. ^abcd"Unusual Analogues: Drugs Used by Gordon Todd Skinner".thislandpress.com. This Land Press. Archived fromthe original on 17 April 2016. Retrieved8 April 2016.
  3. ^abKalir A, Szara S (November 1963). "Synthesis and Pharmacological Activity of Fluorinated Tryptamine Derivatives".Journal of Medicinal Chemistry.6 (6):716–719.doi:10.1021/jm00342a019.PMID 14184932.
  4. ^Halberstadt AL, Geyer MA (2018). "Effect of Hallucinogens on Unconditioned Behavior".Behavioral Neurobiology of Psychedelic Drugs. Current Topics in Behavioral Neurosciences. Vol. 36. pp. 159–199.doi:10.1007/7854_2016_466.ISBN 978-3-662-55878-2.PMC 5787039.PMID 28224459.
  5. ^abNakagawasai O, Arai Y, Satoh SE, Satoh N, Neda M, Hozumi M, Oka R, Hiraga H, Tadano T (January 2004). "Monoamine oxidase and head-twitch response in mice. Mechanisms of alpha-methylated substrate derivatives".Neurotoxicology.25 (1–2):223–232.Bibcode:2004NeuTx..25..223N.doi:10.1016/S0161-813X(03)00101-3.PMID 14697897.
  6. ^Tadano T, Neda M, Hozumi M, Yonezawa A, Arai Y, Fujita T, Kinemuchi H, Kisara K (February 1995). "alpha-Methylated tryptamine derivatives induce a 5-HT receptor-mediated head-twitch response in mice".Neuropharmacology.34 (2):229–234.doi:10.1016/0028-3908(94)00119-d.PMID 7617148.
  7. ^Wagmann L, Brandt SD, Kavanagh PV, Maurer HH, Meyer MR (April 2017)."In vitro monoamine oxidase inhibition potential of alpha-methyltryptamine analog new psychoactive substances for assessing possible toxic risks"(PDF).Toxicol Lett.272:84–93.doi:10.1016/j.toxlet.2017.03.007.PMID 28302559.
  8. ^WO 2022061242, Matthew Baggott, "Advantageous tryptamine compositions for mental disorders or enhancement", published 2023 March 24, assigned toTactogen 

External links

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