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Cyclopropylmescaline

From Wikipedia, the free encyclopedia
Pharmaceutical compound
Cyclopropylmescaline
Clinical data
Other namesCPM; 4-Cyclopropylmethoxy-3,5-methoxyphenethylamine
Routes of
administration
Oral[1]
Drug classSerotonin5-HT2 receptoragonist;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Onset of action≤20 minutes[1]
Duration of action12–18 hours[1]
Identifiers
  • 2-[4-(cyclopropylmethoxy)-3,5-dimethoxyphenyl]ethan-1-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H21NO3
Molar mass251.326 g·mol−1
3D model (JSmol)
  • COc2cc(cc(OC)c2OCC1CC1)CCN
  • InChI=1S/C14H21NO3/c1-16-12-7-11(5-6-15)8-13(17-2)14(12)18-9-10-3-4-10/h7-8,10H,3-6,9,15H2,1-2H3 checkY
  • Key:LNTBHKZMYJTHTH-UHFFFAOYSA-N checkY
  (verify)

Cyclopropylmescaline (CPM), also known as4-cyclopropylmethoxy-3,5-dimethoxyphenethylamine, is apsychedelic drug of thephenethylamine andscaline families related tomescaline.[1] It is takenorally and has a very longduration of 12 to 18 hours.[1]

Use and effects

[edit]

In his bookPiHKAL (Phenethylamines I Have Known and Loved) and other publications,Alexander Shulgin lists the dose range of CPM as 60 to 80 mg and itsduration as 12 to 18 hours.[1][2][3] Itsonset is within 20 minutes and peak effects occurred at around 1.5 hours.[1] The drug is approximately 5 times aspotent as mescaline and is longer-lasting in comparison.[1][2][3]

The effects of CPM have been reported to include remarkableclosed-eye visuals andfantasy,mental imagery synchronized withmusic, not much in terms ofopen-eye visuals, heightenedtactile awareness, not muchinsight,daydreaming abouteroticism, feeling exposed andvulnerable, sounds including voices and even music feeling intrusive andirritating, and interference withsleep and feelingtired due to its very long duration.[1]

Interactions

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

Pharmacology

[edit]

Pharmacodynamics

[edit]

CPM acts as aserotonin5-HT2 receptorfull agonist, including of theserotonin5-HT2A,5-HT2B, and5-HT2C receptors.[4][5]

Chemistry

[edit]

Analogues

[edit]

Analogues of CPM includemescaline,escaline,proscaline,allylescaline,methallylescaline, andcycloproscaline, among others.[1][2]

History

[edit]

CPM was described in thescientific literature byAlexander Shulgin by 1994.[2] Subsequently, it was further described by Shulgin in his 1991 bookPiHKAL (Phenethylamines I Have Known and Loved).[1]

See also

[edit]

References

[edit]
  1. ^abcdefghijkShulgin, Alexander;Shulgin, Ann (September 1991).PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press.ISBN 0-9630096-0-5.OCLC 25627628.CPM Entry inPiHKAL
  2. ^abcdJacob P, Shulgin AT (1994)."Structure-activity relationships of the classic hallucinogens and their analogs".NIDA Res Monogr.146:74–91.PMID 8742795.
  3. ^abShulgin AT (2003)."Basic Pharmacology and Effects". In Laing RR (ed.).Hallucinogens: A Forensic Drug Handbook. Forensic Drug Handbook Series. Elsevier Science. pp. 67–137.ISBN 978-0-12-433951-4.
  4. ^Wallach J, Cao AB, Calkins MM, Heim AJ, Lanham JK, Bonniwell EM, Hennessey JJ, Bock HA, Anderson EI, Sherwood AM, Morris H, de Klein R, Klein AK, Cuccurazzu B, Gamrat J, Fannana T, Zauhar R, Halberstadt AL, McCorvy JD (December 2023)."Identification of 5-HT2A receptor signaling pathways associated with psychedelic potential".Nat Commun.14 (1) 8221.doi:10.1038/s41467-023-44016-1.PMC 10724237.PMID 38102107.
  5. ^Jain MK, Gumpper RH, Slocum ST, Schmitz GP, Madsen JS, Tummino TA, Suomivuori CM, Huang XP, Shub L, DiBerto JF, Kim K, DeLeon C, Krumm BE, Fay JF, Keiser M, Hauser AS, Dror RO, Shoichet B, Gloriam DE, Nichols DE, Roth BL (October 2025). "The polypharmacology of psychedelics reveals multiple targets for potential therapeutics".Neuron.113 (19): 3129–3142.e9.doi:10.1016/j.neuron.2025.06.012.PMID 40683247.

External links

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