DMCPA

Pharmaceutical compound From Wikipedia, the free encyclopedia

DMCPA, also known as 2,5-dimethoxy-4-methylphenylcyclopropylamine, is a psychedelic drug of the phenethylamine, amphetamine, and phenylcyclopropylamine families related to DOM.[1] It is a derivative of tranylcypromine and is the cyclized phenethylamine analogue of DOM in which the α and β positions have been connected with a carbon atom to form a cyclopropyl group.[1]

Other names25D-CPA; 2,5-Dimethoxy-4-methylphenylcyclopropylamine
ATC code
  • None
Quick facts Clinical data, Other names ...
DMCPA
Clinical data
Other names25D-CPA; 2,5-Dimethoxy-4-methylphenylcyclopropylamine
Routes of
administration
Oral[1]
Drug classSerotonin receptor modulator; Serotonergic psychedelic; Hallucinogen
ATC code
  • None
Identifiers
  • 2-(2,5-dimethoxy-4-methylphenyl)cyclopropan-1-amine
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC12H17NO2
Molar mass207.273 g·mol−1
3D model (JSmol)
  • O(c1c(cc(OC)c(c1)C2CC2N)C)C
  • InChI=1S/C12H17NO2/c1-7-4-12(15-3)9(6-11(7)14-2)8-5-10(8)13/h4,6,8,10H,5,13H2,1-3H3 checkY
  • Key:HYVPPECPQRBJEQ-UHFFFAOYSA-N checkY
  (verify)
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Use and effects

In Alexander Shulgin's book PiHKAL (Phenethylamines I Have Known and Loved), the dose range is listed as 15 to 20 mg and the duration is listed as 4 to 8 hours.[1] DMCPA produces open-eye visuals, anorexia, and psychedelic dreams.[1] One of the reports in PiHKAL gave it a +++ on the Shulgin Rating Scale.[1]

Interactions

Pharmacology

Pharmacodynamics

The comprehensive receptor interactions of DMCPA have been studied.[2]

Chemistry

Synthesis

The chemical synthesis of DMCPA has been described.[1]

History

DMCPA was first described in the scientific literature by at least 1974.[3]

Society and culture

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.[4]

See also

References

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