翁坚慧, 徐修容, 朱友成, 周杰, 徐珩, 池志强. 3-甲基芬太尼衍生物构效关系及受体结合特征研究J. 药学学报, 1990, 25(3): 178-185.
引用本文: 翁坚慧, 徐修容, 朱友成, 周杰, 徐珩, 池志强. 3-甲基芬太尼衍生物构效关系及受体结合特征研究J. 药学学报, 1990, 25(3): 178-185.
JH Weng, XR Xu, YC Zhu, J Zhou, H Xu , ZQ Chi, . STUDIES ON STRUCTURE-ACTIVITY RELATIONSHIPS AND RECEPTOR BINDING FEATURE FOR 3-METHYLFENTANYL DERIVATIVESJ. Acta Pharmaceutica Sinica, 1990, 25(3): 178-185.
Citation: JH Weng, XR Xu, YC Zhu, J Zhou, H Xu , ZQ Chi, . STUDIES ON STRUCTURE-ACTIVITY RELATIONSHIPS AND RECEPTOR BINDING FEATURE FOR 3-METHYLFENTANYL DERIVATIVESJ. Acta Pharmaceutica Sinica, 1990, 25(3): 178-185.

3-甲基芬太尼衍生物构效关系及受体结合特征研究

STUDIES ON STRUCTURE-ACTIVITY RELATIONSHIPS AND RECEPTOR BINDING FEATURE FOR 3-METHYLFENTANYL DERIVATIVES

  • 摘要: 对3-甲基芬太尼的1-苯乙基、4-N-丙酰基进行了结构改造、测定了所合成化合物的镇痛活性及部分化合物的镇痛作用持续时间、阿片受体亲和力和对阿片受体亚型的选择性。结果表明,大部分化合物均有较强的吗啡样镇痛活性,强度约为吗啡的2~180倍。所试化合物的镇痛作用持续时间比芬太尼延长6~10倍。化合物1~4的受体亲和力(IC50)约为10-7~10-3mol。化合物13对阿片μ-受体有较高的选择性,对大鼠脑膜的λ/δ比值大于700,对小鼠脑膜的μ/δ比值为1000。

     

    Abstract: Ohmefentanyl is not only a potent analgesic agent, but also a selective ligand for μ opioid receptor, tn order to search for more(?)potent analgesics, more selective lingands and long duration of analgesic action in 3-methylfentanyl derivatives, we made modifications of the 1-phehethyl and 4-N-propionyl groups in 3-methylfentanyl and synthesized 15 new compounds. The analgesic activity, duration of analgesic action, receptor binding affinity and opioid sub-receptor selectivity of some of these compounds were measured. Primary pharmacological results showed that most of the compounds in this series possessed morphine-like effects. Thee analgesic activities of them were about 2~180 times more potent than that of morphine. The duration of analgesic action of the tested compounds was 6~10 times longer than that of fentanyl. The receptor binding affinities (IC50) of compounds 1~4 were. 10-7~10-8 mol. Compound 13 displayed the best binding selectivity on μ opioid receptor site with ratio μ/δ>700 in rat brain membrane and μ/δ=1000 in mouse brain membrane. The new compound may be proposed as a useful tool in studying the opioid receptor. According to the result Of equations in reference 11, compounds 7~14 were designed and prepared. The observed logl/c values of them were much Closer to the calculated values.

     

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