Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

5-MeO-EiPT

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
5-MeO-EiPT
Clinical data
Other names5-Methoxy-N-ethyl-N-isopropyltryptamine
Drug classNon-selectiveserotonin receptor agonist;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Legal status
Legal status
Identifiers
  • N-ethyl-5-methoxy-N-(1-methylethyl)-1H-indole-3-ethanamine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H24N2O
Molar mass260.381 g·mol−1
3D model (JSmol)
  • CC(C)N(CC)CCC1=CNC2=CC=C(OC)C=C21
  • InChI=1S/C16H24N2O/c1-5-18(12(2)3)9-8-13-11-17-16-7-6-14(19-4)10-15(13)16/h6-7,10-12,17H,5,8-9H2,1-4H3
  • Key:VVEQXDHSGNBFLZ-UHFFFAOYSA-N

5-MeO-EiPT, also known as5-methoxy-N-ethyl-N-isopropyltryptamine, is apsychedelic drug of thetryptamine family which has been sold online as adesigner drug.[1][2][3][4]

Use and effects

[edit]

5-MeO-EiPT was not included nor mentioned inAlexander Shulgin's bookTiHKAL (Tryptamines I Have Known and Loved).[5][6] When subsequently asked about 5-MeO-EiPT, Shulgin said that he never got around to making or exploring it and that its dose,duration, and effects were unknown.[6] In any case, 5-MeO-EiPT has been used as a novelrecreationaldesigner drug.[6][4]

Interactions

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

Pharmacology

[edit]

Pharmacodynamics

[edit]

5-MeO-EiPT acts as apotentfull agonist of theserotonin5-HT2A receptor.[3] It also shows highaffinity for the serotonin5-HT1A receptor and interacts very weakly with theserotonin transporter (SERT).[3] The drug produces thehead-twitch response, a behavioral proxy ofpsychedelic effects, in rodents.[3] However, it produces a rather weak head-twitch response, suggesting that it might have reducedhallucinogenic effects relative to other psychedelic tryptamines or might be non-hallucinogenic.[3] The serotonin 5-HT1A receptorantagonistWAY-100635 augmented the head-twitch response induced by 5-MeO-EiPT in rodents.[3] The drug also produceshypothermia andhypolocomotion in rodents.[3]

Chemistry

[edit]

Analogues

[edit]

Analogues of 5-MeO-EiPT includeethylisopropyltryptamine (EiPT),4-HO-EiPT (ethiprocin),4-AcO-EiPT (ethipracetin),5-MeO-DMT,5-MeO-DET,5-MeO-DPT,5-MeO-DiPT,5-MeO-DALT,5-MeO-MET,5-MeO-MPT,5-MeO-MiPT,5-MeO-MsBT,5-MeO-EPT,5-MeO-PiPT, and5-MeO-iPALT (ASR-3001), among others.[5]

History

[edit]

5-MeO-EiPT was first described byAlexander Shulgin by 2002.[6]

Society and culture

[edit]

Legal status

[edit]

5-MeO-EiPT is illegal in Japan.[7]5-MeO-EiPT is illegal in Italy.[8]Sweden's public health agency suggested classifying 5-MeO-EiPT as a hazardous substance, on May 15, 2019.[9][10]

See also

[edit]

References

[edit]
  1. ^"5-MeO-EiPT". Cayman Chemical. Retrieved21 July 2015.
  2. ^Nakazono Y, Tsujikawa K, Kuwayama K, Kanamori T, Iwata YT, Miyamoto K, Kasuya F, Inoue H (January 2014). "Simultaneous determination of tryptamine analogues in designer drugs using gas chromatography–mass spectrometry and liquid chromatography–tandem mass spectrometry".Forensic Toxicology.32 (1):154–161.doi:10.1007/s11419-013-0208-3.S2CID 25134125.
  3. ^abcdefgPuigseslloses P, Nadal-Gratacós N, Ketsela G, Weiss N, Berzosa X, Estrada-Tejedor R, Islam MN, Holy M, Niello M, Pubill D, Camarasa J, Escubedo E, Sitte HH, López-Arnau R (August 2024)."Structure-activity relationships of serotonergic 5-MeO-DMT derivatives: insights into psychoactive and thermoregulatory properties".Mol Psychiatry.29 (8):2346–2358.doi:10.1038/s41380-024-02506-8.PMC 11412900.PMID 38486047.
  4. ^abhttps://isomerdesign.com/bitnest/external/EMCDDA/New-Drugs-In-Europe-2014
  5. ^abShulgin, Alexander;Shulgin, Ann (September 1997).TiHKAL: The Continuation.Berkeley, California:Transform Press.ISBN 0-9630096-9-9.OCLC 38503252.
  6. ^abcd"Ask Dr. Shulgin Online February 27, 2002".keeping freedom in mind -. 27 February 2002. Retrieved12 November 2025.[Derek:] A company that sells chemical novelties has recently begun selling something that they call 5-methoxy-N-ethyl-N-isopropyltryptamine [(5-MeO-EiPT)]. I have searched the Internet, TIHKAL, and other literature for it. I can't find mention of it anywhere. Is it psychoactive? If so what are the effects and what's the dose range? [...] [Shulgin:] the N-ethyl is half-way between [5-MeO-MiPT and 5-MeO-DiPT] and I never did get around to making it. But apparently someone else did. My gut feeling would be to call it 5-MeO-EIPT. But as to predicting the active dosage range and its effects, I would be conservative and cautious.
  7. ^"指定薬物名称・構造式一覧(平成27年9月16日現在)"(PDF) (in Japanese). 厚生労働省. 16 September 2015. Retrieved8 October 2015.
  8. ^"Tabella 1 Sostanze Stupefacenti"(PDF) (in Italian). Governo Italiano. March 2017. Archived fromthe original(PDF) on 6 February 2016. Retrieved27 March 2017.
  9. ^"Folkhälsomyndigheten föreslår att 20 ämnen klassas som narkotika eller hälsofarlig vara" (in Swedish). Folkhälsomyndigheten. 15 May 2019. Archived fromthe original on 20 October 2021. Retrieved11 November 2019.
  10. ^"5-MeO-EIPT".АИПСИН (in Russian). Retrieved7 January 2026.

External links

[edit]
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
Others
Natural sources
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
α-Ketotryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
Retrieved from "https://en.wikipedia.org/w/index.php?title=5-MeO-EiPT&oldid=1338274085"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2026 Movatter.jp