8A-PDHQ

In this article we will explore 8A-PDHQ, a topic of great relevance today that impacts various areas of study and that has generated broad interest in the academic community and society in general. 8A-PDHQ represents a crucial point to understand the functioning of different phenomena, from a historical, scientific, social or cultural perspective. Through detailed analysis, we will examine each relevant aspect of 8A-PDHQ, exploring its implications, its evolution over time, as well as possible solutions or approaches to address this challenge. This article aims to offer a comprehensive, critical and reflective vision about 8A-PDHQ, in an effort to provide knowledge and generate an informed debate on this important topic.

8A-PDHQ
Identifiers
  • 8a-phenyldecahydroquinoline
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC15H21N
Molar mass215.340 g·mol−1
3D model (JSmol)
  • C1(23CCCC2CCCN3)=CC=CC=C1
  • InChI=1S/C15H21N/c1-2-7-13(8-3-1)15-11-5-4-9-14(15)10-6-12-16-15/h1-3,7-8,14,16H,4-6,9-12H2 checkY
  • Key:QEXADSRMRUUCQJ-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

8a-Phenyldecahydroquinoline (8A-PDHQ) is a high affinity NMDA antagonist developed by a team at Parke Davis in the 1950s.[1] It is a structural analog of phencyclidine with slightly lower binding affinity than the parent compound. (−)-8a-Phenyldecahydroquinoline has an in vivo potency comparable to that of (+)-MK-801.[2][3]

References

  1. ^ US Patent 3035059
  2. ^ Chen C, Kozikowski AP, Wood PL, Reynolds IJ, Ball RG, Pang YP (May 1992). "Synthesis and biological activity of 8a-phenyldecahydroquinolines as probes of PCP's binding conformation. A new PCP-like compound with increased in vivo potency". Journal of Medicinal Chemistry. 35 (9): 1634–8. doi:10.1021/jm00087a020. PMID 1315871.
  3. ^ Elhallaoui M, Laguerre M, Carpy A, Ouazzani FC (February 2002). "Molecular modeling of noncompetitive antagonists of the NMDA receptor: proposal of a pharmacophore and a description of the interaction mode". Journal of Molecular Modeling. 8 (2): 65–72. doi:10.1007/s00894-001-0067-4. PMID 12032600. S2CID 34882820.


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