Tenocyclidine

Tenocyclidine
Tenocyclidine.svg
Clinical data
ATC code
  • none
Legal status
Legal status
Identifiers
21500-98-1 ‹See TfM›☒N
62751
DB01520 ☑Y
56495 ☑Y
8BQ45Q6VCL
ChEMBL279676 ☑Y
Chemical and physical data
FormulaC15H23NS
Molar mass249.416 g/mol
3D model (Interactive image
 ‹See TfM›☒N☑Y (verify)

Tenocyclidine (TCP) was discovered by a team at Parke-Davis in the late 1950s.[1] It is a dissociative anesthetic drug with psychostimulant and hallucinogenic effects. 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,[2] but less affinity for the sigma receptors.[3] 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 NMDA receptor antagonist which blocks the activity of the NMDA receptor, however its increased psychostimulant effects compared to PCP suggests it also has relatively greater activity as a dopamine reuptake inhibitor (DRI). Due to its similarity in effects to PCP, TCP was placed into the 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.

Other Languages
español: Tenociclidina
српски / srpski: Tenociklidin
srpskohrvatski / српскохрватски: Tenociklidin