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Fourphit

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This is an old revision of this page, as edited by JCW-CleanerBot (talk | contribs) at 03:04, 13 January 2018 (→top: task, replaced: Pharmacology, biochemistry, and behavior → Pharmacology Biochemistry and Behavior using AWB). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Fourphit
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C18H24N2S/c21-15-19-17-9-13-20(14-10-17)18(11-5-2-6-12-18)16-7-3-1-4-8-16/h1,3-4,7-8,17H,2,5-6,9-14H2
    Key: QAHYIAVTWZVTMY-UHFFFAOYSA-N
  • InChI=1/C18H24N2S/c21-15-19-17-9-13-20(14-10-17)18(11-5-2-6-12-18)16-7-3-1-4-8-16/h1,3-4,7-8,17H,2,5-6,9-14H2
    Key: QAHYIAVTWZVTMY-UHFFFAOYAR
  • c1ccc(cc1)C2(CCCCC2)N3CCC(CC3)N=C=S
Properties
C18H24N2S
Molar mass 300.46 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Fourphit (4-isothiocyanato-1-[1-phenylcyclohexyl]piperidine) is a covalent binding NMDA antagonist, dopaminergic and sigma receptor agonist.[1]

See also

References

  1. ^ Schweri, M. M.; De Costa, B. R.; Rice, K. C. (1998). "Fourphit, an acylating phencyclidine derivative, attenuates cocaine-induced hyperactivity in rats". Pharmacology Biochemistry and Behavior. 60 (3): 615–23. doi:10.1016/s0091-3057(98)00040-9. PMID 9678644.


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