作者:Gui-Bai Liang、Xiaoxia Qian、Dennis Feng、Michael Fisher、Christine M. Brown、Anne Gurnett、Penny Sue Leavitt、Paul A. Liberator、Andrew S. Misura、Tamas Tamas、Dennis M. Schmatz、Matthew Wyvratt、Tesfaye Biftu
DOI:10.1016/j.bmcl.2007.04.041
日期:2007.7
2-a]pyridine derivatives, such as 6a and 7i, have been synthesized and found to be potent inhibitors of parasite PKG activity. The most potent compounds are the 7-isopropylaminomethyl analog 6a and 2-isopropylamino analog 7i. These compounds are also fully active in in vivo assay as anticoccidial agents at 25 ppm in feed.
已经合成了二芳基咪唑并[1,2-a]吡啶衍生物,例如6a和7i,它们是寄生虫PKG活性的有效抑制剂。最有效的化合物是7-异丙基氨基甲基类似物6a和2-异丙基氨基类似物7i。这些化合物作为饲料中25 ppm的抗球虫剂在体内试验中也具有完全活性。