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3',4'-Methylenedioxy-α-pyrrolidinopropiophenone

From Wikipedia, the free encyclopedia
Stimulant drug
Pharmaceutical compound
MDPPP
Clinical data
Routes of
administration
By mouth, insufflation, vaporization, IV, rectal, sublingual
ATC code
  • None
Legal status
Legal status
Pharmacokinetic data
MetabolismHepatic[1][2]
ExcretionPrimarily urine (renal)
Identifiers
  • (RS)-1-(3,4-methylenedioxyphenyl)-2-(1-pyrrolidinyl)-1-propanone
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H17NO3
Molar mass247.294 g·mol−1
3D model (JSmol)
ChiralityRacemic mixture
  • c3c1OCOc1ccc3C(=O)C(C)N2CCCC2
  • InChI=1S/C14H17NO3/c1-10(15-6-2-3-7-15)14(16)11-4-5-12-13(8-11)18-9-17-12/h4-5,8,10H,2-3,6-7,9H2,1H3
  • Key:NIYQOTCYXGXMPI-UHFFFAOYSA-N

3',4'-Methylenedioxy-α-pyrrolidinopropiophenone (MDPPP) is astimulantdesigner drug. It was sold in Germany in the late 1990s and early 2000s as an ingredient in imitationecstasy (MDMA) pills.[3] It shares a similar chemical structure withα-PPP andMDPV,[4][1][2] and has been shown to have reinforcing effects in rats.[5]

Metabolism

[edit]

MDPPP appears to have a similar metabolic fate asMDPV.[2]

Legal status

[edit]

As of October 2015[update] MDPPP is a controlled substance in China.[6]

See also

[edit]

References

[edit]
  1. ^abStaack RF, Maurer HH (June 2005). "Metabolism of designer drugs of abuse".Current Drug Metabolism.6 (3):259–74.doi:10.2174/1389200054021825.PMID 15975043.
  2. ^abcSpringer D, Staack RF, Paul LD, Kraemer T, Maurer HH (March 2005). "Identification of cytochrome P450 enzymes involved in the metabolism of 3',4'-methylenedioxy-alpha-pyrrolidinopropiophenone (MDPPP), a designer drug, in human liver microsomes".Xenobiotica; the Fate of Foreign Compounds in Biological Systems.35 (3):227–37.doi:10.1080/00498250400028239.PMID 16019948.S2CID 28207896.
  3. ^Springer D, Fritschi G, Maurer HH (August 2003). "Metabolism and toxicological detection of the new designer drug 3',4'-methylenedioxy-alpha-pyrrolidinopropiophenone studied in urine using gas chromatography-mass spectrometry".Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences.793 (2):377–88.doi:10.1016/S1570-0232(03)00350-7.PMID 12906913.
  4. ^Maurer HH, Kraemer T, Springer D, Staack RF (April 2004). "Chemistry, pharmacology, toxicology, and hepatic metabolism of designer drugs of the amphetamine (ecstasy), piperazine, and pyrrolidinophenone types: a synopsis".Therapeutic Drug Monitoring.26 (2):127–31.doi:10.1097/00007691-200404000-00007.PMID 15228152.S2CID 9255084.
  5. ^Gannon BM, Galindo KI, Mesmin MP, Sulima A, Rice KC, Collins GT (May 2018)."Relative reinforcing effects of second-generation synthetic cathinones: Acquisition of self-administration and fixed ratio dose-response curves in rats".Neuropharmacology.134 (Pt A):28–35.doi:10.1016/j.neuropharm.2017.08.018.PMC 5809320.PMID 28811192.
  6. ^"关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and Drug Administration. 27 September 2015. Archived fromthe original on 1 October 2015. Retrieved1 October 2015.
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