| 抗棘球蚴药物研究:3-取代苯基-5-取代-1,2,4-噁二唑的合成 |
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| 引用本文： | 高芳华,颜景和.抗棘球蚴药物研究:3-取代苯基-5-取代-1,2,4-噁二唑的合成[J].中国医药工业杂志,1992(6). |
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| 作者姓名： | 高芳华 颜景和 |
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| 作者单位： | 中国预防医学科学院寄生虫病研究所 上海200025 |
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| 摘 要： | 合成了3-取代苯基-5-取代-1,2,4-(口恶)二唑类化合物50个,经感染棘球蚴的小鼠初筛,部分化合物对棘球蚴有不同程度的作用,化合物13、28和30对棘球蚴的囊重抑制率分别为70、75.6和71.6%,其中化合物13对棘球蚴的生发层有损害作用。
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| 关 键 词： | 抗棘球蚴药 3-(4-取代氨基苯基)-5-取代-1 2 4-嚼二唑 3-(4-取代亚甲胺基苯基)-5-取代-1 2 4-噁二唑 |
STUDIES ON ANTIHYDATIC AGENT:SYNTHESIS OF 3-SUBSTITUTED PHENYL-5-SUBSTITUTED-1,2,4-OXADIAZOLES |
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| Authors: | GAO Fang-Hua YAN Jing-He |
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| Abstract: | Fifty 3-substituted phenyl-5-substituted-1,2,4-oxadiazoles havebeen synthesized for screening against Echinococcus granulosus in mice.The cystinhibition rates for 13,28,30 were 70,75.6 and 71.6%,respectively.The germi-nal layer of the hydatid was damaged by 13. |
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| Keywords: | antihydatic agent 3-(4-substituted aminophenyl)-5-substituted-1 2 4-oxadiazole 3-(4-substituted methylene iminophenyl)-5-substituted-1 2 4-oxadiazole |
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