Department of Medicinal Chemistry, ‡Department of Biosciences, and §DMPK and Animal Sciences, AstraZeneca India Pvt. Ltd. , Bellary Road, Hebbal, Bangalore 560024, India.
J Med Chem. 2014 Aug 14;57(15):6642-52. doi: 10.1021/jm500715u. Epub 2014 Jul 21.
From the phenotypic screening of the AstraZeneca corporate compound collection, N-aryl-2-aminobenzimidazoles have emerged as novel hits against the asexual blood stage of Plasmodium falciparum (Pf). Medicinal chemistry optimization of the potency against Pf and ADME properties resulted in the identification of 12 as a lead molecule. Compound 12 was efficacious in the P. berghei (Pb) model of malaria. This compound displayed an excellent pharmacokinetic profile with a long half-life (19 h) in rat blood. This profile led to an extended survival of animals for over 30 days following a dose of 50 mg/kg in the Pb malaria model. Compound 12 retains its potency against a panel of Pf isolates with known mechanisms of resistance. The fast killing observed in the in vitro parasite reduction ratio (PRR) assay coupled with the extended survival highlights the promise of this novel chemical class for the treatment of malaria.
从阿斯利康公司化合物库的表型筛选中,N-芳基-2-氨基苯并咪唑类化合物作为新型抗疟原虫无性血期的有效成分脱颖而出。针对 Pf 的药效和 ADME 性质对该化合物进行了药物化学优化,鉴定出 12 为先导化合物。化合物 12 在疟原虫(Pb)模型中有效。该化合物在大鼠血液中具有出色的药代动力学特性,半衰期(19 小时)长。这种特征使动物在 Pb 疟疾模型中剂量为 50mg/kg 后,存活时间延长了 30 天以上。化合物 12 对具有已知耐药机制的 Pf 分离株保持其效力。在体外寄生虫减少率(PRR)测定中观察到的快速杀伤作用,加上延长的存活时间,突出了这一新型化学类别在治疗疟疾方面的前景。