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Metaphit

Structure via PubChem · Public domain (PubChem)

EntityQ6553528· pop 6· linked from 795 articles

right|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

Wikidata facts

Mass
300.16602
Show 3 more facts
chemical formula
C₁₈H₂₄N₂S
canonical SMILES
C1CCC(CC1)(C2=CC(=CC=C2)N=C=S)N3CCCCC3
Commons category
Metaphit
Sources (2)

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Encyclopedic overview

2 sections
Contents
  • 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.

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