Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

4-AcO-DALT

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
4-AcO-DALT
Clinical data
Other names4-Acetoxy-N,N-diallyltryptamine; Dalcetin
Routes of
administration
Oral
Drug classSerotonergic psychedelic;Hallucinogen
ATC code
  • None
Identifiers
  • [3-[2-[bis(prop-2-enyl)amino]ethyl]-1H-indol-4-yl] acetate
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H22N2O2
Molar mass298.386 g·mol−1
3D model (JSmol)
  • CC(=O)Oc1cccc2c1c(c[nH]2)CCN(CC=C)CC=C
  • InChI=1S/C18H22N2O2/c1-4-10-20(11-5-2)12-9-15-13-19-16-7-6-8-17(18(15)16)22-14(3)21/h4-8,13,19H,1-2,9-12H2,3H3
  • Key:WRHFDIBXZYYCHO-UHFFFAOYSA-N

4-AcO-DALT, also known as4-acetoxy-N,N-diallyltryptamine or asdalcetin, is atryptaminederivative. It has been sold as adesigner drug, but little other information is available. It was first officially identified in seized drug samples in 2012.[1]

Use and effects

[edit]
See also:4-HO-DALT § Use and effects

Interactions

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

Pharmacology

[edit]

Pharmacodynamics

[edit]

4-HO-DALT and 4-AcO-DALT produce thehead-twitch response, a behavioral proxy ofpsychedelic-like effects, in rodents.[2] Thereceptor interactions of 4-HO-DALT and 4-AcO-DALT have been studied.[2][3]

Chemistry

[edit]

Analogues

[edit]

Analogues of 4-AcO-DALT includediallyltryptamine (DALT),4-HO-DALT,5-MeO-DALT,4-AcO-DMT (psilacetin),4-AcO-DET (ethacetin),4-AcO-DiPT (ipracetin), and4-AcO-MALT, among others.

See also

[edit]

References

[edit]
  1. ^EMCDDA–Europol 2012 Annual Report on the implementation of Council Decision 2005/387/JHA (New drugs in Europe, 2012)
  2. ^abKlein LM, Cozzi NV, Daley PF, Brandt SD, Halberstadt AL (November 2018)."Receptor binding profiles and behavioral pharmacology of ring-substituted N,N-diallyltryptamine analogs".Neuropharmacology.142:231–239.doi:10.1016/j.neuropharm.2018.02.028.PMC 6230509.PMID 29499272.
  3. ^Glatfelter GC, Naeem M, Pham DN, Golen JA, Chadeayne AR, Manke DR, Baumann MH (April 2023)."Receptor Binding Profiles for Tryptamine Psychedelics and Effects of 4-Propionoxy-N,N-dimethyltryptamine in Mice".ACS Pharmacol Transl Sci.6 (4):567–577.doi:10.1021/acsptsci.2c00222.PMC 10111620.PMID 37082754.

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-AcO-DALT&oldid=1323752374"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp