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4-PPBP

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4-PPBP
Skeletal formula of 4-PPBP
Ball-and-stick model of the 4-PPBP molecule
Names
Preferred IUPAC name
4-Phenyl-1-(4-phenylbutyl)piperidine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
MeSH 4-phenyl-1-(4-phenylbutyl)piperidine
UNII
  • InChI=1S/C21H27N/c1-3-9-19(10-4-1)11-7-8-16-22-17-14-21(15-18-22)20-12-5-2-6-13-20/h1-6,9-10,12-13,21H,7-8,11,14-18H2[画像:check]Y
    Key:HQGDPZPNAXRCSA-UHFFFAOYSA-N[画像:check]Y
  • InChI=1/C21H27N/c1-3-9-19(10-4-1)11-7-8-16-22-17-14-21(15-18-22)20-12-5-2-6-13-20/h1-6,9-10,12-13,21H,7-8,11,14-18H2
    Key:HQGDPZPNAXRCSA-UHFFFAOYAV
  • C1CN(CCC1C2=CC=CC=C2)CCCCC3=CC=CC=C3
  • c1ccccc1C3CCN(CCCCc2ccccc2)CC3
Properties
C21H27N
Molar mass 293.446 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25°C [77°F], 100kPa).
Chemical compound

4-PPBP is a neuroprotective cyclic amine which binds to sigma receptors.[1]

4-PPBP decreases neuronal nitric oxide synthase (nNOS) activity and ischemia-evoked nitric oxide (NO) production. 4-PPBP provides neuroprotection; this involves the prevention of ischemia-induced intracellular Ca2+ dysregulation.[2] 4-PPBP protects neurons using a mechanism that activates the transcription factor cyclic adenosine monophosphate response element-binding protein (CREB). Neuroprotection that is associated with 4-PPBP increases Bcl-2 expression; Bcl-2 expression is regulated by CREB.[3]

See also

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References

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