Allylnorpethidine
Clinical data
Other namesAllylnorpethidine, WIN-7681
ATC code
  • none
Identifiers
  • Ethyl 4-phenyl-1-(prop-2-en-1-yl)piperidine-4-carboxylate
CAS Number
PubChem CID
ChemSpider
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC17H23NO2
Molar mass273.376 g·mol−1
3D model (JSmol)
  • O=C(OCC)C2(c1ccccc1)CCN(C\C=C)CC2
  • InChI=1S/C17H23NO2/c1-3-12-18-13-10-17(11-14-18,16(19)20-4-2)15-8-6-5-7-9-15/h3,5-9H,1,4,10-14H2,2H3 checkY
  • Key:YUNKDDDGCRLMAF-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Allylnorpethidine (WIN-7681) is a 4-phenylpiperidine derivative that is related to the opioid analgesic drug pethidine (meperidine).

Allylnorpethidine is an analogue of pethidine where the N-methyl group has been replaced by allyl. In many other opioid derivatives, placing an allyl substituent on the nitrogen instead of a methyl will reverse the normal opioid effects, to produce μ-opioid antagonists which among other things reverse the respiratory depression caused by opioid agonists such as morphine. This is not true with allylnorpethidine, as while it does partially reverse the respiratory depression produced by morphine[1] it is actually an active analgesic and has no antagonistic properties[2][3] when administered alone, so is instead a partial agonist.

References

  1. ↑ Costa PJ, Bonnycastle DD (March 1955). "The effect of levallorphan tartrate, nalorphine HCl and WIN 7681 (1-allyl-4-phenyl-4-carbethoxypiperidine) on respiratory depression and analgesia induced by some active analgetics". The Journal of Pharmacology and Experimental Therapeutics. 113 (3): 310–8. PMID 14368499.
  2. ↑ Casy AF, Parfitt RT (1986). Opioid Analgesics: Chemistry and Receptors. Springer. p. 239. ISBN 0-306-42130-5.
  3. ↑ Stenlake JB (1979). Foundations of Molecular Pharmacology. p. 152. ISBN 0-485-11171-3.(online version)
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