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Studies on the Synthesis, Anticonvulsant Activity, and the Structure-Activity Relationships of Phenyl Pyridazinones and their GABA Derivatives

苯基哒嗪酮及其GABA衍生物的合成、抗惊活性及构效关系的研究
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摘要 In searching for effective anticonvulsant agents,fourteen 6-aryl-4.5-di- hydro-3(2H)pyridazinones.fifteen 6-aryl-3(2H)pyridazinones,and seventeen 3-GABA derivatives of 6-aryIpyridazines have been synthesized,and evaluated in mice for the ability to antagonize maximal electroshock seizure(MES).The ED_(50) values showed that 6-(2′,4′- dichlorophenyt)-3(2H)pyridazinone was the most potent anticonvulsant among these corn- pounds(ED_(50)=10.15 mg/kg).The structure-activity relationships of the aryl pyridazinones were studied.The result showed that:(1)the higher the value of the hydrophobic parameter л of the substituent on the phenyl ring.the more potent the anticonvulsant activity of the corn- pound.and(2)only the compounds with an electron withdrawing substituent on the phenyl ring exhibited appreciable anticonvulsant activity. 本文报道了14个6-芳基-4,5-二氢-3(2H)哒嗪酮,15个6-芳基-3(2H)哒嗪酮和17个6-芳基哒嗪的3位GABA衍生物的合成及其抗电惊活性。活性最强的是2′,4′-二氯苯基-3(2H)哒嗪酮(ED_(50)=10.15mg/kg)。对芳基哒嗪酮类的构效分析表明,苯环上的取代基对化合物的抗惊活性有明显影响,吸电子取代基和疏水性参数值较大的取代基有利于提高化合物的抗惊活性。
出处 《Journal of Chinese Pharmaceutical Sciences》 CAS 1992年第2期27-34,共8页 中国药学(英文版)
关键词 Aryl pyridazinones 3-GABA-6-aryl pyridazines Anticonvulsant activity Structure-activity relationships 芳基哒嗪酮 3-GABA-6-芳基哒嗪 抗惊活性 构效关系
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