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Jimscaline

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Jimscaline
Clinical data
Other namesC-(4,5,6-Trimethoxyindan-1-yl)methanamine
Drug classSerotonin receptor modulator;Serotonin 5-HT2A receptor agonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • (4,5,6-trimethoxy-2,3-dihydro-1H-inden-1-yl)methanamine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H19NO3
Molar mass237.299 g·mol−1
3D model (JSmol)
  • COC1=C(C(=C2CCC(C2=C1)CN)OC)OC
  • InChI=1S/C13H19NO3/c1-15-11-6-10-8(7-14)4-5-9(10)12(16-2)13(11)17-3/h6,8H,4-5,7,14H2,1-3H3 ☒N
  • Key:AFTIZGHFDCOQFS-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Jimscaline, also known asC-(4,5,6-trimethoxyindan-1-yl)methanamine, is aconformationally-restrictedderivative of thecactus-derivedpsychedelic drugmescaline, which was reported in 2006 by a team atPurdue University led byDavid E. Nichols. It acts as apotentagonist for theserotonin5-HT2A and5-HT2Creceptors with the more active (R)-enantiomer having anaffinity (Ki) of 69 nM at the human serotonin 5-HT2A receptor, and around three times the potency of mescaline indrug discrimination tests in animals.[1] This discovery that theside chain of the psychedelicphenethylamines could beconstrained to givechiral ligands with increased activity then led to the later development of the highly-potentbenzocyclobutene derivativeTCB-2.[2][3] Jimscaline is not acontrolled substance inCanada as of 2025.[4]

(R)-Jimscaline.

See also

[edit]

References

[edit]
  1. ^McLean TH, Chambers JJ, Parrish JC, Braden MR, Marona-Lewicka D, Kurrasch-Orbaugh D, Nichols DE (July 2006). "C-(4,5,6-trimethoxyindan-1-yl)methanamine: a mescaline analogue designed using a homology model of the 5-HT2A receptor".Journal of Medicinal Chemistry.49 (14):4269–74.CiteSeerX 10.1.1.690.1860.doi:10.1021/jm060272y.PMID 16821786.
  2. ^McLean TH, Parrish JC, Braden MR, Marona-Lewicka D, Gallardo-Godoy A, Nichols DE (September 2006). "1-Aminomethylbenzocycloalkanes: conformationally restricted hallucinogenic phenethylamine analogues as functionally selective 5-HT2A receptor agonists".Journal of Medicinal Chemistry.49 (19):5794–803.CiteSeerX 10.1.1.688.9849.doi:10.1021/jm060656o.PMID 16970404.
  3. ^Braden MR (2007).Towards a biophysical understanding of hallucinogen action (Ph.D. thesis). Purdue University.ProQuest 304838368.
  4. ^"Controlled Drugs and Substances Act".Department of Justice Canada. Retrieved19 January 2026.

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