Department of Chemistry, University of Oslo , P.O. Box 1033, Blindern, N-0315 Oslo, Norway.
J Med Chem. 2014 Jun 26;57(12):5464-9. doi: 10.1021/jm500503k. Epub 2014 Jun 16.
We report the synthesis and biological evaluation of a triplet of 6-O-(18)F-fluoroethylated derivatives of structurally related orvinols that span across the full range of intrinsic activities, the antagonist diprenorphine, the partial agonist buprenorphine, and the full agonist phenethyl-orvinol. [(18)F]fluoroethyl-diprenorphine, [(18)F]fluoroethyl-buprenorphine, and [(18)F]fluoroethyl-phenethyl-orvinol were prepared in high yields and quality from their 6-O-desmethyl-precursors. The results indicate suitable properties of the three 6-O-(18)F-fluoroethylated derivatives as functional analogues to the native carbon-11 labeled versions with similar pharmacological properties.
我们报告了一系列结构相关的奥芬醇的 6-O-(18)F-氟乙基化衍生物的合成和生物学评价,这些衍生物涵盖了内在活性的全范围,包括拮抗剂地普诺啡、部分激动剂丁丙诺啡和完全激动剂苯乙基-奥芬醇。[(18)F]氟乙基-地普诺啡、[(18)F]氟乙基-丁丙诺啡和[(18)F]氟乙基-苯乙基-奥芬醇从其 6-O-去甲前体以高产率和高质量制备。结果表明,这三种 6-O-(18)F-氟乙基化衍生物具有作为天然碳-11 标记版本的功能类似物的合适性质,具有相似的药理学性质。