Chemistry:4-PPBP
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| Names | |
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| Preferred IUPAC name
4-Phenyl-1-(4-phenylbutyl)piperidine | |
| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
| MeSH | 4-phenyl-1-(4-phenylbutyl)piperidine |
PubChem CID
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| 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], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
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
References
- ↑ "Sigma receptor agonists provide neuroprotection in vitro by preserving bcl-2". Anesthesia and Analgesia 104 (5): 1179–84, tables of contents. May 2007. doi:10.1213/01.ane.0000260267.71185.73. PMID 17456670.
- ↑ "Sigma receptor ligand 4-phenyl-1-(4-phenylbutyl)-piperidine modulates neuronal nitric oxide synthase/postsynaptic density-95 coupling mechanisms and protects against neonatal ischemic degeneration of striatal neurons". Experimental Neurology 221 (1): 166–74. January 2010. doi:10.1016/j.expneurol.2009.10.019. PMID 19883643.
- ↑ "Cyclic adenosine monophosphate response element-binding protein phosphorylation and neuroprotection by 4-phenyl-1-(4-phenylbutyl) piperidine (PPBP)". Anesthesia and Analgesia 108 (3): 964–70. March 2009. doi:10.1213/ane.0b013e318192442c. PMID 19224810.
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