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Propylallyltryptamine

From Wikipedia, the free encyclopedia
Pharmaceutical compound
Propylallyltryptamine
Clinical data
Other namesPALT;N-Propyl-N-allyltryptamine; ASR-3004; ASR3004
Drug classSerotonin receptor modulator;Serotonin 5-HT2A receptor agonist
ATC code
  • None
Identifiers
  • N-[2-(1H-indol-3-yl)ethyl]-N-prop-2-enylpropan-1-amine
PubChemCID
ChemSpider
Chemical and physical data
FormulaC16H22N2
Molar mass242.366 g·mol−1
3D model (JSmol)
  • CCCN(CCC1=CNC2=CC=CC=C21)CC=C
  • InChI=1S/C16H22N2/c1-3-10-18(11-4-2)12-9-14-13-17-16-8-6-5-7-15(14)16/h3,5-8,13,17H,1,4,9-12H2,2H3
  • Key:BPHDZENPKNMIRD-UHFFFAOYSA-N

Propylallyltryptamine (PALT), also known asN-propyl-N-allyltryptamine or by its developmental code nameASR-3004, is aserotonin receptor modulator of thetryptamine family.[1] It is an asymmetricalanalogue ofdipropyltryptamine (DPT) anddiallyltryptamine (DALT).[1] The drug is anon-selectiveserotonin receptor agonist, including of theserotonin5-HT1B,5-HT2A,5-HT2B, and5-HT6 receptors, but not of the serotonin5-HT1A receptor.[1] It is also aserotonin–norepinephrine–dopamine reuptake inhibitor (SNDRI).[1] Thechemical synthesis of PALT has been described.[1] A notableanalogue of PALT isiPALT (ASR-3003).[1] PALT waspatented by theAlexander Shulgin Research Institute (ASRI) in 2024.[1]

See also

[edit]

References

[edit]
  1. ^abcdefgUS 20240277665A1, Daley PF, Cozzi NV, Callaway WB, "Asymmetric allyl tryptamines", issued 4 March 2024, assigned to Alexander Shulgin Research Institute Inc. 
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
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