Fourphit
Appearance
From Wikipedia, the free encyclopedia
This is an old revision of this page, as edited by Rjwilmsi (talk | contribs) at 19:29, 4 August 2016 (→top: Journal cites, Added 1 doi to a journal cite using AWB (12061)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
![]() | |
Identifiers | |
---|---|
CompTox Dashboard (EPA)
|
|
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).
|
Chemical compound
Fourphit (4-isothiocyanato-1-[1-phenylcyclohexyl]piperidine) is a covalent binding NMDA antagonist, dopaminergic and sigma receptor agonist.[1]
See also
References
- ^ 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.
|
σ1 |
|
---|---|
σ2 |
|
Unsorted |
|
See also: Receptor/signaling modulators |
![]() | This drug article relating to the nervous system is a stub. You can help Wikipedia by expanding it. |
Retrieved from "https://en.wikipedia.org/w/index.php?title=Fourphit&oldid=733011545"
Hidden categories:
- Chemical articles without CAS registry number
- Chemicals without a PubChem CID
- Articles without InChI source
- Chemical pages without ChemSpiderID
- Articles without EBI source
- Articles without KEGG source
- Articles without UNII source
- Articles containing unverified chemical infoboxes
- Chembox image size set
- Articles with short description
- Short description matches Wikidata
- All stub articles