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Trimethoxyamphetamines

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(Redirected fromTMA-4 (psychedelic))
Chemical compound

Trimethoxyamphetamines (TMAs) are a family ofpositionally isomericpsychedelichallucinogenicdrugs.[1][2] There exist six different TMAs that differ only in the positions of the threemethoxygroups:TMA (TMA-1),TMA-2, TMA-3, TMA-4, TMA-5, andTMA-6.[1][2] The TMAs aresubstituted amphetamines and areanalogues of thephenethylaminecactusalkaloidmescaline and theDOx drugs.[1][2]

Themechanism of action of the TMAs is different from that of the unsubstituted compoundamphetamine, probably involvingagonist activity onserotonin receptors such as the5-HT2A receptors instead of themonoamine releasing agent actions typical of most amphetamines. This action on serotonergic receptors likely underlies the psychedelic effects of these compounds.

TMA was firstsynthesized by Hey, in 1947.[3] Synthesis data as well ashuman activity data has been published byAlexander Shulgin in his bookPiHKAL.[1][2]

The most important TMA compound from a pharmacological standpoint is TMA-2, as this isomer has been much more widely used as arecreational drug and sold on thegrey market as a so-calledresearch chemical; TMA (sometimes referred to as "mescalamphetamine" or TMA-1) and TMA-6 have also been used in this way to a lesser extent. These three isomers are significantly more active as hallucinogenic drugs, and have consequently been placed onto the illegal drug schedules in some countries such as theNetherlands andJapan. The other three isomers TMA-3, TMA-4, and TMA-5 are not known to have been used as recreational drugs to any great extent. According to Shulgin, at the doses tested, TMA-3 was completely inactive, whereas TMA-4 and TMA-5 were said to produce effects comparable tolysergic acid diethylamide (LSD).[1]

2,4,6-TMA (TMA-6) is apotentmonoamine oxidase A (MAO-A)inhibitor, with anIC50Tooltip half-maximal inhibitory concentration of 400 nM.[4] Conversely, 2,4,5-TMA (TMA-2) and 3,4,5-TMA (TMA-1) are inactive as MAO-A inhibitors (IC50 = >100,000 nM).[4] Other 6-substituted amphetamines also tend to be potent MAO-A inhibitors.[4]

List of TMAs

[edit]
TMA
Chemical name1-(3,4,5-Trimethoxyphenyl)propan-2-amine,
3,4,5-trimethoxyamphetamine,
α-methylmescaline
Melting point220 - 221 °C (hydrochloride)
SMILESNC(C)CC1=CC(OC)=C(OC)C(OC)=C1
CAS number
1082-88-8
Chemical structure of TMA
Chemical structure of TMA
UNII_Ref = checkYUNII = P2K02L3YON
TMA-2
Chemical name1-(2,4,5-Trimethoxyphenyl)propan-2-amine,
2,4,5-trimethoxyamphetamine
Melting point188.5 - 189.5 °C (hydrochloride)
SMILESNC(C)CC1=C(OC)C=C(OC)C(OC)=C1
CAS number
1083-09-6
Chemical structure of TMA-2
Chemical structure of TMA-2
UNII_Ref = checkYUNII = 713Z3SL0TJ
TMA-3
Chemical name1-(2,3,4-Trimethoxyphenyl)propan-2-amine,
2,3,4-trimethoxyamphetamine
Melting point148 - 149 °C (hydrochloride)
SMILESNC(C)CC1=CC=C(OC)C(OC)=C1OC
CAS number
1082-23-1
Chemical structure of TMA-3
Chemical structure of TMA-3
UNII_Ref = checkYUNII = 9T3SO4A6HM

TMA-4
Chemical name1-(2,3,5-Trimethoxyphenyl)propan-2-amine,
2,3,5-trimethoxyamphetamine
Melting point118 - 119 °C (hydrochloride)
SMILESNC(C)CC1=CC(OC)=CC(OC)=C1OC
CAS number
23693-14-3
Chemical structure of TMA-4
Chemical structure of TMA-4
UNII_Ref = checkYUNII = LEL94CV318
TMA-5
Chemical name1-(2,3,6-Trimethoxyphenyl)propan-2-amine,
2,3,6-trimethoxyamphetamine
Melting point124 - 125 °C (hydrochloride)
SMILESNC(C)CC1=C(OC)C=CC(OC)=C1OC
CAS number
20513-16-0
Chemical structure of TMA-5
Chemical structure of TMA-5
UNII_Ref = checkYUNII = E0NJ557A3E
TMA-6
Chemical name1-(2,4,6-Trimethoxyphenyl)propan-2-amine,
2,4,6-trimethoxyamphetamine
Melting point207 - 208 °C (hydrochloride)
SMILESNC(C)CC1=C(OC)C=C(OC)C=C1OC
CAS number
15402-79-6
Chemical structure of TMA-6
Chemical structure of TMA-6
UNII_Ref = checkYUNII = 2X84DCO6GA

Note: Because they are isomers, the TMAs have the samechemical formula, C12H19NO3, and the samemolecular mass, 225.28 g/mol.

Use and effects[1]

[edit]
CompoundPatternDoseDurationEffects
TMA3,4,5100 – 250 mg6 - 8 hPsychedelic
TMA-22,4,520 – 40 mg8 - 12 hPsychedelic
TMA-32,3,4> 100 mgunknownNone
TMA-42,3,5≥ 80 mg~ 6 hPsychedelic
TMA-52,3,6≥ 30 mg8 - 10 hStimulant, psychedelic
TMA-62,4,625 – 50 mg12 - 16 hPsychedelic

Society and culture

[edit]

Legal status

[edit]

Brazil

[edit]

It is scheduled in theF2 class (prohibited psychotropics) of theBrazilian Controlled Drugs and Substances Act.[5][which?]

Sweden

[edit]

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 byMedical Products Agency in their regulation LVFS 2004:3 listed as 2,4,5-trimetoxiamfetamin (TMA-2).[6]

United Kingdom

[edit]

Illegal under thePsychoactive Substances Act 2016.[which?]

United States of America

[edit]

3,4,5-Trimethoxyamphetamine is listed as a Schedule 1 controlled substance, along with positional isomers 2,4,5-Trimethoxyamphetamine (TMA-2), 2,4,6-Trimethoxyamphetamine (TMA-6) andescaline.[7]

See also

[edit]

References

[edit]
  1. ^abcdefShulgin AT, Shulgin A (1991).PiHKAL: A Chemical Love Story (1st ed.). Berkeley, CA: Transform Press.ISBN 9780963009609.OCLC 25627628.
  2. ^abcdShulgin A, Manning T, Daley PF (2011).The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds. Vol. 1. Berkeley: Transform Press.ISBN 978-0-9630096-3-0.
  3. ^Hey, P (1947). "The synthesis of a new homologue of mescaline".Quart. J. Pharm. Pharmacol.20 (2):129–134.PMID 20260568.
  4. ^abcReyes-Parada M, Iturriaga-Vasquez P, Cassels BK (2019)."Amphetamine Derivatives as Monoamine Oxidase Inhibitors".Front Pharmacol.10 1590.doi:10.3389/fphar.2019.01590.PMC 6989591.PMID 32038257.
  5. ^Anvisa (2023-07-24)."RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese).Diário Oficial da União (published 2023-07-25).Archived from the original on 2023-08-27. Retrieved2023-08-27.
  6. ^"Läkemedelsverkets föreskrifter - LVFS och HSLF-FS" [The Swedish Medicines Agency's regulations - LVFS and HSLF-FS](PDF) (in Swedish).
  7. ^"Lists of: Scheduling Actions Controlled Substances Regulated Chemicals"(PDF). April 2024. Retrieved2024-07-17.

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