顺-3-甲基芬太尼的4-N-丙酰基结构类似物的合成与镇痛活性及构效关系的研究
SYNTHESIS,ANALGESIC ACTIVITY AND STUCTUREACTIVITY RELATIONSHIP OF 4-N-PROPIONYL ANALOGS OF CIS-3-METHYL FENTANYL
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摘要: 以不同电性的基团取代顺-3-甲基芬太尼中4-N-丙酰基上的乙基,合成某些顺-3-甲基芬太尼的结构类似物。药理试验结果表明,所合成的化合物均有典型的吗啡样作用。化合物3的镇痛活性略强于顺-3-甲基芬太尼。应用半经验的INDO方法对4个代表化合物进行了量子化学计算,讨论了电子结构与镇痛活性间的关系,化合物3由于氯乙烯基的引入具有与顺-3-甲基芬太尼不同的电子结构特征,氯乙烯基可能作为电子接受体参与了与受体的作用。Abstract: The synthesis of some 4-N-propionyl analogs of cis-3-methylfentanyl by acyl chloride method, anhydride method, mixed anhydride method and DCCmethod is reported. The ethyl group in 4-N-propionyl portion of cis-3-methylfentanyl was substituted by some groups with different electronic property. In mouse hotplate test. all compounds showed typical morphine-like action with analgesic potency cor-responding to 49~1963 times that of morphine. Compound 3 was found to exhibit higheranalgesic activity than cis-3-methyl fentanyl. Semiempirical INDO calculationshave been undertaken for 4 typical compounds and it was found that as a result of in-troduction of chlorovinyl, compound 3 exhibited characteristics of electronic structuredifferent from that of cis-3-methyl fentanyl. The relationships between analgesic activityand the electronic structure of these compounds were discussed.
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