Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

4-HO-NiPT

From Wikipedia, the free encyclopedia

Pharmaceutical compound
4-HO-NiPT
Clinical data
Other names4-Hydroxy-N-isopropyltryptamine; 4-Hydroxy-NiPT; 4-HO-NIPT
Drug classSerotonin receptor modulator;Serotonin 5-HT2A receptor agonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Identifiers
  • 3-[2-(propan-2-ylamino)ethyl]-1H-indol-4-ol
PubChemCID
Chemical and physical data
FormulaC13H18N2O
Molar mass218.300 g·mol−1
3D model (JSmol)
  • CC(C)NCCC1=CNC2=C1C(=CC=C2)O
  • InChI=1S/C13H18N2O/c1-9(2)14-7-6-10-8-15-11-4-3-5-12(16)13(10)11/h3-5,8-9,14-16H,6-7H2,1-2H3
  • Key:YJBOZZRZZJEXDB-UHFFFAOYSA-N

4-HO-NiPT, also known as4-hydroxy-N-isopropyltryptamine, is aserotonin receptor modulator and putativepsychedelic drug of thetryptamine and4-hydroxytryptamine families related topsilocin (4-HO-DMT).[1][2][3] It is ananalogue of4-HO-MiPT (miprocin) and4-HO-DiPT (iprocin) and aderivative ofnorpsilocin (4-HO-NMT) and4-HO-NET.[2] The drug has been encountered online as a possible noveldesigner drug.[4]

Use and effects

[edit]

4-HO-NiPT was not included nor mentioned inAlexander Shulgin's bookTiHKAL (Tryptamines I Have Known and Loved).[5]

Interactions

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

Pharmacology

[edit]

Pharmacodynamics

[edit]

4-HO-NiPT showsaffinity forserotonin receptors, including for theserotonin5-HT1D,5-HT1E,5-HT2A,5-HT2B,5-HT2C,5-HT6, and5-HT7 receptors (Ki = 229–2,461 nM).[2] Conversely, it did not show affinity for the serotonin5-HT1B or5-HT5A receptors, whereas the serotonin5-HT1A receptor was not reported.[2] 4-HO-NiPT is apartial agonist of the serotonin 5-HT2A, 5-HT2B, and 5-HT2C receptors, withEC50Tooltip half-maximal effective concentration (EmaxTooltip maximal efficacy) values of 24 nM (88.4%), 188 nM (69.9%), and 963 nM (45.2%), respectively.[2] It was also anagonist of other serotonin receptors, including the serotonin 5-HT1B, 5-HT1E,5-HT1F, and 5-HT7A receptors (EC50 = 1.4–23 nM,Emax = 20.4–123%), but not of the 5-HT1A, 5-HT1D,5-HT4, 5-HT5A, or 5-HT6 receptors.[2]

In contrast to norpsilocin, but similarly to psilocin and certain otherN-monoalkyltryptamines like 4-HO-NET,4-HO-NPT,4-HO-NALT, and4-HO-NBnT, the drug produces thehead-twitch response, a behavioral proxy of psychedelic effects, in rodents.[2] It showed 30-fold lowerpotency than psilocin in this action in mice, but produced about the same maximal response.[2] Similarly to 4-HO-NiPT, otherN-monoalkyltryptamines were also much less potent than psilocin, in the range of 10- to 26-fold less potent.[2] In addition to the head-twitch response, 4-HO-NiPT produceshypothermia in rodents.[2]

4-HO-NiPT is a knownmetabolite of4-AcO-DiPT and presumably also of4-HO-DiPT.[1]

Chemistry

[edit]

Synthesis

[edit]

Thechemical synthesis of 4-HO-NiPT has been described.[1][2]

Analogues

[edit]
4-HO-NET,4-HO-NPT, 4-HO-NiPT, and4-HO-NBnT.

Analogues of 4-HO-NiPT include4-hydroxytryptamine (4-HT or 4-HO-T),4-HO-MiPT (miprocin),4-HO-DiPT (diprocin),psilocin (4-HO-DMT),norpsilocin (4-HO-NMT),4-HO-NET,4-HO-NPT,4-HO-NALT, and4-HO-NBnT, among others.[2]

History

[edit]

4-HO-NiPT was first described in thescientific literature, as ametabolite of4-AcO-DiPT, in 2022.[6] Subsequently, itssynthesis was described in 2023[1] and itspharmacology was reported in 2024.[2] The drug was reported as a possible noveldesigner drug online in 2022.[4]

See also

[edit]

References

[edit]
  1. ^abcdLaban U, Naeem M, Chadeayne AR, Golen JA, Manke DR (March 2023)."Synthesis and structure of 4-hy-droxy-N-iso-propyl-tryptamine (4-HO-NiPT) and its precursors".Acta Crystallographica. Section e, Crystallographic Communications.79 (Pt 4):280–286.Bibcode:2023AcCrE..79..280L.doi:10.1107/S2056989023002098.PMC 10088304.PMID 37057027.
  2. ^abcdefghijklmSherwood AM, Burkhartzmeyer EK, Williamson SE, Baumann MH, Glatfelter GC (January 2024)."Psychedelic-like Activity of Norpsilocin Analogues".ACS Chemical Neuroscience.15 (2):315–327.doi:10.1021/acschemneuro.3c00610.PMC 10797613.PMID 38189238.
  3. ^Naeem M, Manke DR, Neto CA, Chadeayne AR (2024).Synthetic & structural investigations of novel metal-chelate complexes and tryptamine derivatives: a dissertation in Chemistry and Biochemistry (Doctor of Philosophy thesis). University of Massachusetts Dartmouth.doi:10.62791/2002. Retrieved23 November 2025.
  4. ^ab"4-HO-NIPT (4-hydroxy NiPT)".АИПСИН (in Russian). Retrieved23 November 2025.
  5. ^Shulgin A,Shulgin A (September 1997).TiHKAL: The Continuation.Berkeley, California:Transform Press.ISBN 0-9630096-9-9.OCLC 38503252.
  6. ^Malaca S, Huestis MA, Lattanzio L, Marsella LT, Tagliabracci A, Carlier J, et al. (July 2022)."Human Hepatocyte 4-Acetoxy-N,N-Diisopropyltryptamine Metabolite Profiling by Reversed-Phase Liquid Chromatography Coupled with High-Resolution Tandem Mass Spectrometry".Metabolites.12 (8): 705.doi:10.3390/metabo12080705.PMC 9413566.PMID 36005577.

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
  • Bioisosteres:JRT
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
Cyclized tryptamines
Isotryptamines
Related compounds
Retrieved from "https://en.wikipedia.org/w/index.php?title=4-HO-NiPT&oldid=1323801925"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp