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苯甲吗啉 1,2,4,5-四氧杂环戊烷类似物 N205 的合成与分析:开发具有单剂量治愈疟疾潜力的四氧杂环戊烷骨架。

Synthesis and profiling of benzylmorpholine 1,2,4,5-tetraoxane analogue N205: Towards tetraoxane scaffolds with potential for single dose cure of malaria.

机构信息

Department of Chemistry, University of Liverpool, Liverpool L69 7ZD, United Kingdom.

Department of Chemistry, University of Liverpool, Liverpool L69 7ZD, United Kingdom.

出版信息

Bioorg Med Chem. 2018 Jul 15;26(11):2996-3005. doi: 10.1016/j.bmc.2018.05.006. Epub 2018 May 17.

DOI:10.1016/j.bmc.2018.05.006
PMID:29779669
Abstract

A series of aryl carboxamide and benzylamino dispiro 1,2,4,5-tetraoxane analogues have been designed and synthesized in a short synthetic sequence from readily available starting materials. From this series of endoperoxides, molecules with in vitro IC50s versus Plasmodium falciparum (3D7) as low as 0.84 nM were identified. Based on an assessment of blood stability and in vitro microsomal stability, N205 (10a) was selected for rodent pharmacokinetic and in vivo antimalarial efficacy studies in the mouse Plasmodium berghei and Plasmodium falciparum Pf3D70087/N9 severe combined immunodeficiency (SCID) mouse models. The results indicate that the 4-benzylamino derivatives have excellent profiles with a representative of this series, N205, an excellent starting point for further lead optimization studies.

摘要

已经从易得的起始原料出发,通过一个简短的合成序列,设计并合成了一系列芳基酰胺和苄氨基双螺 1,2,4,5-四噁烷类似物。从这一系列过氧化物中,鉴定出了对体外 Plasmodium falciparum (3D7) 的 IC50 值低至 0.84nM 的分子。基于对血液稳定性和体外微粒体稳定性的评估,选择 N205(10a)进行啮齿动物药代动力学和体内抗疟功效研究,在小鼠 Plasmodium berghei 和 Plasmodium falciparum Pf3D70087/N9 严重联合免疫缺陷(SCID)小鼠模型中进行。结果表明,4-苄氨基衍生物具有优异的特性,该系列的代表化合物 N205 是进一步进行先导化合物优化研究的良好起点。

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