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Synthesis, structural and biological characterization of 5-phenylhydantoin derivatives as potential anticonvulsant agents

机译:5-苯基乙内酰脲衍生物作为潜在的抗惊厥药的合成,结构和生物学特性

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Considering the importance of hydantoin derivatives in treatment of status epilepticus, four 5-phen-ylhydantoins, whose lipophilicities were estimated to be similar to that of phenytoin, were synthesized. Evaluation of their anticonvulsant activities was performed on rats by subcutaneous pentylenetetrazol seizure test and intravenous pentylenetetrazol threshold test, and spontaneous locomotor activity test was used to assess possible sedative effects. X-ray analysis of three compounds suggested that certain analogies might be drawn between interactions in crystal packing and biological interactions responsible for their anticonvulsant activity. It was found that 5-ethyl-5-phenyl-3-propylhydantoin exhibits the most favorable pharmacological properties among the synthesized compounds, i.e., anticonvulsant activity comparable to phenytoin with lower liability for induction of sedation in rats.
机译:考虑到乙内酰脲衍生物在治疗癫痫持续状态中的重要性,据估计合成了四个亲脂性与苯妥英相似的5-苯乙酰乙内酰脲。通过皮下戊四氮癫痫发作试验和静脉内戊四氮阈值试验评价它们的抗惊厥活性,并使用自发运动活性试验评估可能的镇静作用。对三种化合物的X射线分析表明,可能在晶体堆积的相互作用与负责其抗惊厥活性的生物学相互作用之间得出某些类比。已发现5-乙基-5-苯基-3-丙基乙内酰脲在合成的化合物中表现出最有利的药理性质,即,与苯妥英钠相当的抗惊厥活性,对大鼠镇静的诱导作用较低。

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