Faxeladol

Chemical compound
  • None
Identifiers
  • 3-[(1R,2R)-2-dimethylaminomethylcyclohexyl]phenol
CAS Number
  • 433265-65-7 checkY
PubChem CID
  • 9813414
ChemSpider
  • 7989164 checkY
UNII
  • C04V6SGK8H
KEGG
  • D10007 ☒N
CompTox Dashboard (EPA)
  • DTXSID20912318 Edit this at Wikidata
Chemical and physical dataFormulaC15H23NOMolar mass233.355 g·mol−13D model (JSmol)
  • Interactive image
  • Oc1cccc(c1)[C@@H]2CCCC[C@H]2CN(C)C
InChI
  • InChI=1S/C15H23NO/c1-16(2)11-13-6-3-4-9-15(13)12-7-5-8-14(17)10-12/h5,7-8,10,13,15,17H,3-4,6,9,11H2,1-2H3/t13-,15-/m0/s1 checkY
  • Key:JIRYWFYYBBRJAN-ZFWWWQNUSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Faxeladol (INN, USAN) (code names GRTA-9906, GRTA-0009906, EM-906, GCR-9905, GRT-TA300) is an opioid analgesic which was developed by Grünenthal GmbH but was never marketed for medical use anywhere in the world. It is related to tramadol and ciramadol, and was developed shortly after tramadol in the late 1970s. Similarly to tramadol, it was believed faxeladol would have analgesic, as well as antidepressant effects, due to its action on serotonin and norepinephrine reuptake. In various studies in the 1970s alongside tramadol, faxeladol was seen to be slightly more potent than tramadol, but with a higher rate of sudden seizures than tramadol, which is known to cause seizures without warning in some users.

See also

References


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