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JWH-161

From Wikipedia, the free encyclopedia
Chemical
Pharmaceutical compound
JWH-161
Identifiers
  • (4aR,13bR)-2,5,5-trimethyl-8-pentyl-3,4,4a,5,8,13b-hexahydroisochromeno[3,4-b]carbazol-13-ol
CAS Number
PubChemCID
ChemSpider
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Chemical and physical data
FormulaC27H33NO2
Molar mass403.566 g·mol−1
3D model (JSmol)
  • Oc3c5c1ccccc1n(c5cc2OC([C@@H]4CC/C(=C\[C@H]4c23)C)(C)C)CCCCC
  • InChI=1S/C27H33NO2/c1-5-6-9-14-28-21-11-8-7-10-18(21)24-22(28)16-23-25(26(24)29)19-15-17(2)12-13-20(19)27(3,4)30-23/h7-8,10-11,15-16,19-20,29H,5-6,9,12-14H2,1-4H3/t19-,20-/m1/s1
  • Key:VDJUAFPNHZRTNL-WOJBJXKFSA-N
  (verify)

JWH-161 is a cannabinoid derivative that was designed by DrJohn W. Huffman's team as a hybrid between thedibenzopyran "classical"cannabinoid drugs and the novelindole derivatives, in an attempt to unravel the differences in their binding modes to the CB1 receptor. While retaining structural elements from both families, JWH-161 has aCB1Ki of 19.0nM, although it was found to be slightly weaker thanTHC in animal tests.[1]

References

[edit]
  1. ^Huffman JW, Padgett LW (2005). "Recent developments in the medicinal chemistry of cannabimimetic indoles, pyrroles and indenes".Current Medicinal Chemistry.12 (12):1395–411.doi:10.2174/0929867054020864.PMID 15974991.
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