4-Phenyl-4-(1-piperidinyl)cyclohexanol

Source: Wikipedia, the free encyclopedia.
4-Phenyl-4-(1-piperidinyl)cyclohexanol
Names
Preferred IUPAC name
4-Phenyl-4-(piperidin-1-yl)cyclohexan-1-ol
Other names
4-Phenyl-4-(1-piperidinyl)cyclohexanol
Identifiers
3D model (
JSmol
)
ChemSpider
UNII
  • InChI=1S/C17H25NO/c19-16-9-11-17(12-10-16,15-7-3-1-4-8-15)18-13-5-2-6-14-18/h1,3-4,7-8,16,19H,2,5-6,9-14H2 checkY
    Key: KPRUAZBLIREHPD-UHFFFAOYSA-N checkY
  • InChI=1/C17H25NO/c19-16-9-11-17(12-10-16,15-7-3-1-4-8-15)18-13-5-2-6-14-18/h1,3-4,7-8,16,19H,2,5-6,9-14H2
    Key: KPRUAZBLIREHPD-UHFFFAOYAM
  • OC1CCC(N2CCCCC2)(C3=CC=CC=C3)CC1
  • OC3CCC(c1ccccc1)(N2CCCCC2)CC3
Properties
C17H25NO
Molar mass 259.391 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

4-Phenyl-4-(1-piperidinyl)cyclohexanol, also known as PPC, is an organic chemical which is a metabolite of phencyclidine (PCP).[1] It can be detected in the hair of PCP users.[2]

PPC has been shown to cause increases in

locomotor activity in lab mice.[3]

See also

  • PCHP, another PCP metabolite

References

  1. ^ Nabeshima, Toshitaka; Yamaguchi, Kazumasa; Fukaya, Hiroaki; Hiramatsu, Masayuki; Furukawa, Hiroshi; Kameyama, Tsutomu (1985). "Simultaneous determination of phencyclidine and its major metabolites in biological samples by high-performance liquid chromatography". Research Communications in Substances of Abuse. 6 (2): 65–78.
  2. PMID 9288587
    .
  3. ^ "Behavioral effects of phencyclidine and its major metabolite, (trans)4-phenyl-4-(1-piperidinyl)cyclohexanol, in mice".
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