Synthesis and hypnotic-sedative activities of N-substituted uracil on mice.

Tokumi Maruyama, Shigetada Kozai, Tomomi Shimizu, Toshiyuki Kimura, Kazuhito Watanabe, Ikuo Yamamoto
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引用次数: 3

Abstract

N3-Phenacyl-N1-substituted uracils 3a-q were synthesized by introduction of substituents at the N1-position of N3-phenacyluracil 2, and their hypnotic and sedative activities were evaluated. Pharmacological activities of these N3-phenacyl-N1-substituted uracils were examined using hypnotic activity and synergistic effects with pentobarbital or diazepam for the hypnotic and sedative activities.

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n -取代尿嘧啶的合成及对小鼠的催眠镇静作用。
通过在N3-phenacyluracil 2的n1位上引入取代基,合成n3 -phenacyl - n1取代尿嘧啶3a-q,并对其催眠和镇静活性进行了评价。利用催眠活性和与戊巴比妥或地西泮的协同作用来研究这些n3 -phenacyl- n1取代尿嘧啶的药理活性。
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