Structure via PubChem · Public domain (PubChem)
Metaphit
Sign in to saveright|thumb|250px|class=skin-invert-image|Metaphit as a methanesulfonate salt
Chemical data
- Formula
- C18H24N2S
- Molecular weight
- 300.5 g/mol
- IUPAC name
- 1-[1-(3-isothiocyanatophenyl)cyclohexyl]piperidine
via PubChem
~1 min read
Encyclopedic overview
2 sectionsContents
- See also
- References
right|thumb|250px|class=skin-invert-image|Metaphit as a methanesulfonate salt
Metaphit (1-[1-(3-Isothiocyanato)phenyl]cyclohexylpiperidine) is a research chemical that acts as an acylator of NMDARAn, sigma and DAT binding sites in the CNS. It is the m-isothiocyanate derivative of phencyclidine (PCP) and binds irreversibly (forming a covalent bond) to the PCP binding site on the NMDA receptor complex. However, later studies suggest the functionality of metaphit is mediated by sites not involved in PCP-induced passive avoidance deficit, and not related to the NMDA receptor complex. Metaphit was also shown to prevent d-amphetamine induced hyperactivity, while significantly depleting dopamine content in the nucleus accumbens. Metaphit was the first acylating ligand used to study the cocaine receptor. It is a structural isomer of the similar research compound fourphit, as it and metaphit both are isothiocyanate substituted derivatives of an analogous scaffold shared with PCP.
Excerpted from Wikipedia’s “Metaphit” article, available under the CC BY-SA 4.0 licence.