Dexoxadrol

Chemical compound
  • none
Legal statusLegal status
  • In general: legal
Identifiers
  • (2S)-2-[(4S)-2,2-Di(phenyl)-1,3-dioxolan-4-yl]piperidine
CAS Number
  • 4741-41-7 checkY
PubChem CID
  • 3034023
ChemSpider
  • 2298576 checkY
UNII
  • JY5N9F45AG
ChEMBL
  • ChEMBL1165411 checkY
CompTox Dashboard (EPA)
  • DTXSID50912321 Edit this at Wikidata
Chemical and physical dataFormulaC20H23NO2Molar mass309.409 g·mol−13D model (JSmol)
  • Interactive image
  • O1C[C@@H](OC1(c2ccccc2)c3ccccc3)[C@H]4NCCCC4
InChI
  • InChI=1S/C20H23NO2/c1-3-9-16(10-4-1)20(17-11-5-2-6-12-17)22-15-19(23-20)18-13-7-8-14-21-18/h1-6,9-12,18-19,21H,7-8,13-15H2/t18-,19+/m0/s1 checkY
  • Key:HGKAMARNFGKMLC-RBUKOAKNSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Dexoxadrol (Dioxadrol) is a dissociative anaesthetic drug which has been found to be an NMDA antagonist and produces similar effects to PCP in animals. Dexoxadrol, along with another related drug etoxadrol, were developed as analgesics for use in humans, but development was discontinued after patients reported side effects such as nightmares and hallucinations.[1][2]

See also

  • WMS-2539, a fluorinated derivative of dexoxadrol

References

  1. ^ Sax M, Wünsch B (2006). "Relationships between the structure of dexoxadrol and etoxadrol analogues and their NMDA receptor affinity". Current Topics in Medicinal Chemistry. 6 (7): 723–32. doi:10.2174/156802606776894483. PMID 16719812.
  2. ^ Aepkers M, Wünsch B (December 2005). "Structure-affinity relationship studies of non-competitive NMDA receptor antagonists derived from dexoxadrol and etoxadrol". Bioorganic & Medicinal Chemistry. 13 (24): 6836–49. doi:10.1016/j.bmc.2005.07.030. PMID 16169732.
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