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4-AcO-DiPT

From Wikipedia, the free encyclopedia
(Redirected from4-Acetoxy-DiPT)
Pharmaceutical compound
4-AcO-DiPT
Clinical data
Other names4-Acetoxy-DiPT; 4-Acetoxy-N,N-diisopropyltryptamine
Routes of
administration
Oral[1]
Drug classNon-selectiveserotonin receptor agonist;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Identifiers
  • 3-{2-[di(propan-2-yl)amino]ethyl}-1H-indol-4-yl acetate
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H26N2O2
Molar mass302.418 g·mol−1
3D model (JSmol)
  • CC(C)N(CCc1c[nH]c2c1c(ccc2)OC(=O)C)C(C)C
  • InChI=1S/C18H26N2O2/c1-12(2)20(13(3)4)10-9-15-11-19-16-7-6-8-17(18(15)16)22-14(5)21/h6-8,11-13,19H,9-10H2,1-5H3
  • Key:ZPAOVGZYDSXCPK-UHFFFAOYSA-N
  (verify)

4-AcO-DiPT, also known as4-acetoxy-N,N-diisopropyltryptamine or asipracetin, is apsychedelic drug of thetryptamine and4-hydroxytryptamine families related to4-AcO-DMT (psilacetin).[1][2] It is takenorally.[1]

The drug is thought to likely be aprodrug of4-HO-DiPT, which acts as anon-selectiveserotonin receptor agonist including of theserotonin5-HT2A receptor.[3][2] It produces psychedelic-like effects in animals.[2]

4-AcO-DiPT was first described in thescientific literature byAlexander Shulgin by 2003.[1] It was encountered as a noveldesigner drug in 2005.[2][4][5]

Use and effects

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See also:4-HO-DiPT § Use and effects

According toAlexander Shulgin in a 2003literature review, the dose range of 4-AcO-DiPT is 6 to 10 mgorally.[1] For comparison, the dose range of4-HO-DiPT is listed as 15 to 20 mg in the same review.[1]

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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4-AcO-DiPT is thought to be likely to function asprodrug of4-HO-DiPT, althoughpharmacokinetic studies are still needed to confirm this.[3][2] It acts as aserotonin5-HT2 receptoragonist, albeit with greatly reducedpotency relative to4-HO-DiPT.[2] The drug produces thehead-twitch response, a behavioral proxy ofpsychedelic effects, in rodents.[2]

Chemistry

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4-AcO-DiPT is atryptamine and isstructurally similar to4-HO-DiPT,psilocin (4-HO-DMT), and4-AcO-DMT (psilacetin).[1][2]

Analogues

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Analogues of 4-AcO-DiPT includediisopropyltryptamine (DiPT),4-HO-DiPT (iprocin),4-PrO-DiPT,luvesilocin (4-GO-DiPT),4-AcO-DMT (psilacetin),4-AcO-DET (ethacetin),4-AcO-DPT (depracetin), and4-AcO-DALT (dalcetin), among others.

History

[edit]

4-AcO-DiPT was first described in thescientific literature byAlexander Shulgin by 2003.[1] It was encountered as a noveldesigner drug in 2005.[2][4][5]

Society and culture

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Legal status

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Denmark

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4-AcO-DiPT is added to the list of Schedule B controlled substances.[6]

Japan

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4-AcO-DiPT is a controlled substance in Japan.[7]

Sweden

[edit]

Sveriges riksdags health ministryStatens folkhälsoinstitut classified 4-AcO-DiPT as "health hazard" under the actLagen om förbud mot vissa hälsofarliga varor (translatedAct on the Prohibition of Certain Goods Dangerous to Health) as of Mar 1, 2005, in their regulation SFS 2005:26 listed as 4-acetoxi-N,N-diisopropyltryptamin (4-AcO-DIPT), making it illegal to sell or possess.[8]

United States

[edit]

4-AcO-DiPT is an unscheduled substance in the United States. Due to similarities to other scheduled tryptamines, such asdiethyltryptamine and psilocin, possession may be prosecuted under theFederal Analog Act in the United States.

See also

[edit]

References

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  1. ^abcdefghShulgin AT (2003)."Basic Pharmacology and Effects". In Laing RR (ed.).Hallucinogens: A Forensic Drug Handbook. Forensic Drug Handbook Series. Elsevier Science. pp. 67–137.ISBN 978-0-12-433951-4.
  2. ^abcdefghiKlein AK, Chatha M, Laskowski LJ, Anderson EI, Brandt SD, Chapman SJ, McCorvy JD, Halberstadt AL (April 2021)."Investigation of the Structure-Activity Relationships of Psilocybin Analogues".ACS Pharmacol Transl Sci.4 (2):533–542.doi:10.1021/acsptsci.0c00176.PMC 8033608.PMID 33860183.
  3. ^abKozell LB, Eshleman AJ, Swanson TL, Bloom SH, Wolfrum KM, Schmachtenberg JL, Olson RJ, Janowsky A, Abbas AI (April 2023)."Pharmacologic Activity of Substituted Tryptamines at 5-Hydroxytryptamine (5-HT)2A Receptor (5-HT2AR), 5-HT2CR, 5-HT1AR, and Serotonin Transporter".J Pharmacol Exp Ther.385 (1):62–75.doi:10.1124/jpet.122.001454.PMC 10029822.PMID 36669875.
  4. ^abhttps://isomerdesign.com/bitnest/external/EMCDDA/New-Drugs-In-Europe-2005
  5. ^abRodriguez-Cruz, S. E. (2005). Analysis and Characterization of Designer Tryptamines using Electrospray Ionization Mass Spectrometry (ESI-MS).Microgram,3(3–4), 107–129.https://forendex.southernforensic.org/uploads/references/MicrogramJournal/3.3-4.107.129.pdf
  6. ^"Bekendtgørelse om euforiserende stoffer - retsinformation.dk".
  7. ^"指定薬物一覧|厚生労働省". Retrieved23 December 2011.
  8. ^"1Svensk författningssamling"(PDF). www.notisum.se. 3 February 2005. Archived fromthe original(PDF) on 2013-09-29. Retrieved2020-03-24.

External links

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