作者:Keith A. M. Walker、Eric B. Sjogren、Thomas R. Matthews
DOI:10.1021/jm00149a023
日期:1985.11
Screening of mesoionic compounds as potential electron acceptors by analogy with metronidazole led to the finding of in vitro antitrichomonal activity for anhydro-2-phenyl-3-hydroxythiazolo [3,2-a]pyridinium hydroxide (1). In a series of analogues, potent in vitro activity was found to be associated with amino substitution; however, such activity was dependent on specific structural features and not
通过与甲硝唑类比筛选作为潜在电子受体的中离子化合物,发现了对脱水-2-苯基-3-羟基噻唑[3,2-a]吡啶鎓氢氧化物的体外抗滴虫活性(1)。在一系列类似物中,发现有效的体外活性与氨基取代有关。但是,这种活性取决于特定的结构特征,而不取决于还原潜力。活性最高的化合物仅显示出较差的体内活性。