A series of 2-imino-6-methyltetrahydropyrimidin-4(1H)-one derivatives, substituted in the 6-position by a phenyl moiety which in turn is meta-substituted by an optionally substituted unsaturated fused bicyclic ring system containing at least one nitrogen atom, being selective inhibitors of plasmepsin V activity, are beneficial as pharmaceutical agents, especially in the treatment of malaria.
一系列 2-亚
氨基-6-甲基四氢
嘧啶-4(1H)-酮衍
生物,在 6 位被苯基取代,而苯基又被含有至少一个氮原子的任选取代的不饱和融合双环体系元取代,是胰
蛋白酶 V 活性的选择性
抑制剂,可用作药物,特别是治疗疟疾。