Tenocyclidine

Source: Wikipedia, the free encyclopedia.
Tenocyclidine
Clinical data
ATC code
  • none
Legal status
Legal status
Identifiers
  • 1-(1-(2-Thienyl)cyclohexyl)piperidine
JSmol)
  • C1(C2(CCCCC2)N3CCCCC3)=CC=CS1
  • InChI=1S/C15H23NS/c1-3-9-15(10-4-1,14-8-7-13-17-14)16-11-5-2-6-12-16/h7-8,13H,1-6,9-12H2 checkY
  • Key:JUZZEWSCNBCFRL-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Tenocyclidine (TCP) is a

psychostimulant effects. It was discovered by a team at Parke-Davis in the late 1950s.[2] It is similar in effects to phencyclidine (PCP) but is considerably more potent. TCP has slightly different binding properties to PCP, with more affinity for the NMDA receptors,[3] but less affinity for the sigma receptors.[4] Because of its high affinity for the PCP site of the NMDA receptor complex, the 3H radiolabelled
form of TCP is widely used in research into NMDA receptors.

TCP acts primarily as an

Schedule I list of illegal drugs in the 1970s, although it was only briefly used in the 1970s and 1980s and is now little known.[citation needed
]

See also

References

  1. ^ Anvisa (2023-07-24). "RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-07-25). Archived from the original on 2023-08-27. Retrieved 2023-08-27.
  2. ^ U.S. patent 2,921,076 Heterocyclic compounds and methods for producing the same
  3. S2CID 35120805
    .
  4. .