Within the frame of the design of prodrug candidates to deliver a C-alkylamidine antimalarial agent, we showed that specific O-substitutions were needed on the alkylamidoxime structure. Among the newly synthesized molecules, bis-oxadiazolone and bis-O-methylsulfonylamidoxime derivatives induced a complete clearance of parasitemia in mice after oral administration.
在设计用于递送C-烷基am抗疟剂的前药候选物的框架内,我们表明在烷基ami
肟结构上需要特定的O-取代。在新合成的分子中,双-
恶二唑酮和双-O-甲基磺酰酰胺基
肟衍
生物在口服后可诱导小鼠体内完全清除寄生虫病。