The Wayback Machine - https://web.archive.org/web/20120112081137/http://en.wikipedia.org:80/wiki/4-MeO-PCP

4-MeO-PCP

From Wikipedia, the free encyclopedia
Jump to: navigation, search
4-MeO-PCP
Systematic (IUPAC) name
1-[1-(4-methoxyphenyl)cyclohexyl]-piperidine
Clinical data
Pregnancy cat.  ?
Legal status Not Currently Scheduled
Identifiers
CAS number 2201-35-6
91164-58-8 (hydrochloride)
ATC code None
PubChem CID 11778080
ChemSpider 10526416 YesY
Chemical data
Formula C18H27NO 
Mol. mass 273.412 g/mol
SMILES eMolecules & PubChem
 YesY(what is this?)  (verify)

4-Methoxyphencyclidine (methoxydine, 4-MeO-PCP) is a dissociative anesthetic drug with hallucinogenic and sedative effects. It is around the same potency as ketamine, but has slightly different effects due to its altered binding profile at various targets, particularly being somewhat more potent as an NMDA antagonist while having around the same potency as a dopamine reuptake inhibitor.[1][2][3][4]

The positional isomer 3-MeO-PCP is also known. Being around 10 times more potent by weight than the 4-methoxy isomer it has around the same potency as PCP. 4-Meo-PCP was reportedly first sold within the UK from 2008 as a designer drug and research chemical by a company trading under the name CBAY.[5]

[edit] See also

[edit] References

  1. ^ Vignon J, Vincent JP, Bidard JN, Kamenka JM, Geneste P, Monier S, Lazdunski M (July 1982). "Biochemical properties of the brain phencyclidine receptor". European Journal of Pharmacology 81 (4): 531–42. doi:10.1016/0014-2999(82)90342-9. PMID 6214413. 
  2. ^ Manallack DT, Wong MG, Costa M, Andrews PR, Beart PM (December 1988). "Receptor site topographies for phencyclidine-like and sigma drugs: predictions from quantitative conformational, electrostatic potential, and radioreceptor analyses". Molecular Pharmacology 34 (6): 863–79. PMID 2849051. 
  3. ^ Chaudieu I, Vignon J, Chicheportiche M, Kamenka JM, Trouiller G, Chicheportiche R (March 1989). "Role of the aromatic group in the inhibition of phencyclidine binding and dopamine uptake by PCP analogs". Pharmacology, Biochemistry, and Behavior 32 (3): 699–705. doi:10.1016/0091-3057(89)90020-8. PMID 2544905. 
  4. ^ Manallack DT, Davies JW, Beart PM, Saunders MR, Livingstone DJ (October 1993). "Analysis of the biological and molecular properties of phencyclidine-like compounds by chemometrics". Arzneimittel-Forschung 43 (10): 1029–32. PMID 8267664. 
  5. ^ [King LA. New drugs coming our way - what are they and how do we detect them? EMCDDA Conference, Lisbon, 6–8 May 2009 http://www.emcdda.europa.eu/attachements.cfm/att_78745_EN_4_King.pps]


Personal tools
Namespaces
Variants
Actions
Navigation
Interaction
Toolbox
Print/export
Morty Proxy This is a proxified and sanitized view of the page, visit original site.