Chemistry:4-HO-DiPT

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Short description: Chemical compound
4-HO-DiPT
4-HO-DIPT.SVG
4-HO-DiPT-3d-sticks.png
Clinical data
Routes of
administration
Oral
Legal status
Legal status
  • DE: NpSG (Industrial and scientific use only)
  • UK: Class A
  • US: Unscheduled
Pharmacokinetic data
Elimination half-life1-2 hrs
Identifiers
CAS Number
ChemSpider
UNII
Chemical and physical data
FormulaC16H24N2O
Molar mass260.381 g·mol−1
3D model (JSmol)
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4-HO-DiPT Powder
4-HO-DiPT Powder

4-Hydroxy-N,N-diisopropyltryptamine (4-HO-DiPT or Iprocin) is a synthetic psychedelic drug. It is a higher homologue of psilocin, 4-HO-DET, and is a positional isomer of 4-HO-DPT and has a tryptamine molecular sub-structure.

Dosage

4-HO-DiPT is orally active at around 3 mg and above, and its effects last for 2–3 hours.[1] Higher doses such as those above 30 mgs can increase the duration of the effects significantly.

Effects

The effects of 4-HO-DiPT are broadly comparable to those of other serotonergic psychedelics such as LSD and psilocin, but they are distinguished by their relative brevity. Shulgin "doubt[s] that there is another psychedelic drug, anywhere, that can match this one for speed, for intensity, for brevity, and sensitivity to dose, at least one that is active orally." An idiosyncratic effect of the drug, also noted by Shulgin, is its tendency to induce tremors.[2][3][4]

Some users have reported a minor audio distortion with lower dosages. Higher dosages increase the polarity of the distortion. It is defined as being slightly lower in pitch and creating several different effects, such as pitch bend, volume distortion, and rate distortion. As with most DiPT psychedelics, music can become more dissonant and less harmonious. Users have also reported a visual distortion widely comparable to the hallucinogen LSD.

Pharmacology

Pharmacodynamics

Binding Sites Binding Affinity Ki (μM) Action [5]
5-HT1A 5.7 ???
5-HT2A 0.728 partial agonist
5-HT2C 2.8 ???
D1 >25 ???
D2 >25 ???
D3 >25 ???
α1A >12 ???
α2A 15 ???
TAAR1 >15 ???
H1 9.8 ???
SERT 1.8 inhibitor
DAT >26 inhibitor
NET 11 inhibitor

Clinical trials

FT-104, a prodrug to 4-HO-DiPT, has entered double blind, randomized, placebo controlled, phase 1 clinical trials in healthy volunteers at the Royal Adelaide Hospital in Australia for the treatment of postpartum depression and treatment-resistant depression. [6][7][8]

FT-104 [1]

Legal status

Finland

Scheduled in government decree on psychoactive substances banned from the consumer market.[9]

Germany

Scheduled in New Psychoactive Substances Act (NpSG). Use of covered substances is permitted only for industrial and scientific purposes.

Sweden

Sveriges riksdags health ministry Statens folkhälsoinstitut classified 4-HO-DiPT as "health hazard" under the act Lagen om förbud mot vissa hälsofarliga varor (translated Act on the Prohibition of Certain Goods Dangerous to Health) as of Mar 1, 2005, in their regulation SFS 2005:26 listed as 4-hydroxi-N,N-diisopropyltryptamin (4-HO-DIPT), making it illegal to sell or possess.[10]

United States

4-HO-DiPT is not scheduled at the federal level in the United States ,[11] but it is possible that it could be considered an analog of 5-MeO-DiPT, in which case purchase, sale, or possession could be prosecuted under the Federal Analog Act.

Florida

"4-Hydroxy-N,N-diisopropyltryptamine" is a Schedule I controlled substance in the state of Florida making it illegal to buy, sell, or possess in Florida.[12]

References

  1. "Erowid 4-HO-DiPT Vault : Dosage". https://www.erowid.org/chemicals/4_ho_dipt/4_ho_dipt_dose.shtml. Retrieved 8 April 2023. 
  2. Shulgin, Alexander; Shulgin, Ann (September 1997). TiHKAL: The Continuation. Berkeley, California: Transform Press. ISBN 0-9630096-9-9. OCLC 38503252. http://www.erowid.org/library/books_online/tihkal/tihkal.shtml. 
  3. "4-Hydroxy-DIPT". Erowid. https://www.erowid.org/chemicals/4_ho_dipt/4_ho_dipt.shtml. 
  4. "Tihkal 4-HO-DIPT entry". https://www.erowid.org/library/books_online/tihkal/tihkal17.shtml. 
  5. "Receptor interaction profiles of novel psychoactive tryptamines compared with classic hallucinogens". European Neuropsychopharmacology 26 (8): 1327–37. August 2016. doi:10.1016/j.euroneuro.2016.05.001. PMID 27216487. http://edoc.unibas.ch/53326/1/20170117174852_587e4af45b658.pdf. 
  6. "Field Trip Announces First Dosings in Phase I Clinical Study of FT-104" (Press release). 21 July 2022.
  7. "An Inside Look into Field Trip's Next-Generation Psychedelic, FT-104". 11 August 2022. https://psychedelicspotlight.com/an-inside-look-into-field-trips-next-generation-psychedelic-ft-104/. 
  8. "WIPO - Search International and National Patent Collections". https://patentscope.wipo.int/search/en/detail.jsf;?docId=US346005716. Retrieved 8 April 2023. 
  9. "FINLEX ® - Säädökset alkuperäisinä: Valtioneuvoston asetus kuluttajamarkkinoilta… 1130/2014". https://www.finlex.fi/fi/laki/alkup/2014/20141130. Retrieved 8 April 2023. 
  10. "Svensk författningssamling" (in Swedish). http://www.notisum.se/rnp/sls/sfs/20050026.pdf. 
  11. "21 CFR — SCHEDULES OF CONTROLLED SUBSTANCES §1308.11 Schedule I.". http://www.deadiversion.usdoj.gov/21cfr/cfr/1308/1308_11.htm. 
  12. "Statutes & Constitution :View Statutes : Online Sunshine". http://leg.state.fl.us/statutes/index.cfm?App_mode=Display_Statute&URL=0800-0899/0893/0893.html. Retrieved 8 April 2023. 

External links