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

作　　者：翁坚慧 徐修容[2] 朱友成[2] 周杰[2] 徐珩[2] 池志强[2] 

机构地区：[1]中国科学院上海药物研究所1986届 [2]中国科学院上海药物研究所,上海200031

出　　处：《药学学报》1990年第3期178-185,共8页Acta Pharmaceutica Sinica

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(IC_(50))约为10^(-7)～10^(-3)mol。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。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 (IC_(50)) 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.

关 键 词：甲基芬太尼 镇痛活性 受体亲和力 

分 类 号：R962[医药卫生—药理学]