Carr J B, Durham H G, Hass D K
J Med Chem. 1977 Jul;20(7):934-9. doi: 10.1021/jm00217a014.
A series of 3-halo-5-phenyl- and 3-phenyl-5-haloisoxazoles has demonstrated anthelmintic activity at doses ranging from 16 to 500 mg/kg orally against the rat roundworm, Nippostrongylus braziliensis. In the 5-phenyl series a halogen at the 3 position of the isoxazole ring was required for activity. However, in the 3-phenyl series activity was maintained after replacement of the 5-halogen with certain alkoxyl, thioalkoxyl, or amino groups. The 3-phenyl and 5-phenyl series apparently are not acting biologically at a common receptor site. Synthetic methods and structure-activity relationships are discussed.
一系列3-卤代-5-苯基异恶唑和3-苯基-5-卤代异恶唑已证明,口服剂量为16至500mg/kg时,对巴西日圆线虫具有驱虫活性。在5-苯基系列中,异恶唑环3位上的卤素是活性所必需的。然而,在3-苯基系列中,用某些烷氧基、硫代烷氧基或氨基取代5-卤素后仍保持活性。3-苯基系列和5-苯基系列显然不是在共同的受体位点发挥生物学作用。讨论了合成方法和构效关系。