Boss C, Richard-Bildstein S, Weller T, Fischli W, Meyer S, Binkert C
Drug Discovery Chemistry, Actelion Pharmaceuticals Ltd., Gewerbestrasse 16, CH-4123 Allschwil / BL, Switzerland.
Curr Med Chem. 2003 Jun;10(11):883-907. doi: 10.2174/0929867033457674.
Malaria is a very serious infectious disease against which the currently available drugs are loosing effectiveness. The main problem is the emergence and the spreading of resistant parasite strains. New treatments are needed in order to regain control over the disease. Drug discovery efforts towards this goal are likely to be more successful, if they focus towards novel mechanisms of action. Such efforts will result in drugs that are functionally and structurally different from the existing drugs and therefore will overcome existing resistances. Here we focus on the aspartic protease plasmepsin II, which is a promising new drug target. We review the drug discovery efforts that were published in the literature on this enzyme, and we present the compounds synthesized at Actelion Pharmaceuticals Ltd.
疟疾是一种非常严重的传染病,目前可用的药物正逐渐失去效力。主要问题是耐药寄生虫菌株的出现和传播。为了重新控制这种疾病,需要新的治疗方法。如果药物研发工作专注于新的作用机制,朝着这一目标的努力可能会更成功。这样的努力将产生在功能和结构上与现有药物不同的药物,从而克服现有的耐药性。在这里,我们聚焦于天冬氨酸蛋白酶疟原虫胃蛋白酶II,它是一个有前景的新药物靶点。我们回顾了文献中发表的关于这种酶的药物研发工作,并展示了Actelion制药有限公司合成的化合物。