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抗寄生虫药。6. 新型异硫氰酸苯酯基-1,2,4-恶二唑的合成及其驱虫活性

Antiparasitic agents. 6. Synthesis and anthelmintic activities of novel isothiocyanatophenyl-1,2,4-oxadiazoles.

作者信息

Haugwitz R D, Martinez A J, Venslavsky J, Angel R G, Maurer B V, Jacobs G A, Narayanan V L, Cruthers L R, Szanto J

出版信息

J Med Chem. 1985 Sep;28(9):1234-41. doi: 10.1021/jm00147a019.

Abstract

The syntheses and anthelmintic activities of 31 3- and 5-(isothiocyanatophenyl)-1,2,4-oxadiazoles are reported. In the primary anthelmintic screen, 3-(4-isothiocyanatophenyl)-1,2,4-oxadiazole (39) showed 100% nematocidal activity and 3-(2-furanyl)-5-(4-isothiocyanatophenyl)-1,2,4-oxadiazole (63), 3-(2-furanyl)-5-(2-chloro-4-isothiocyanatophenyl)-1,2,4-oxadiazole (64), and 3-(2-furanyl)-5-(4-chloro-3-isothiocyanatophenyl)-1,2,4-oxadiazole (66) showed 100% taeniacidal activity when administered orally to mice. The two most active members of this series, 39 and 63, were active against the gastrointestinal nematodes of sheep at 100 mg/kg. In addition, 39 was also found to be active against hookworms in dogs at a single, oral dose of 200 mg/kg.

摘要

报道了31种3-和5-(异硫氰酸苯酯基)-1,2,4-恶二唑的合成及其驱虫活性。在初步驱虫筛选中,3-(4-异硫氰酸苯酯基)-1,2,4-恶二唑(39)表现出100%的杀线虫活性,而3-(2-呋喃基)-5-(4-异硫氰酸苯酯基)-1,2,4-恶二唑(63)、3-(2-呋喃基)-5-(2-氯-4-异硫氰酸苯酯基)-1,2,4-恶二唑(64)和3-(2-呋喃基)-5-(4-氯-3-异硫氰酸苯酯基)-1,2,4-恶二唑(66)经口给予小鼠时表现出100%的杀绦虫活性。该系列中活性最高的两个成员,即39和63,在100mg/kg时对绵羊胃肠道线虫具有活性。此外,还发现39以200mg/kg的单次口服剂量对犬钩虫有活性。

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