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重新利用传染病药物作为先导化合物。

Repurposing Infectious Disease Hits as Anti- Leads.

机构信息

Department of Medicine Division of Allergy Infectious Disease Center for Emerging Reemerging Infectious Diseases, University of Washington, Seattle, Washington 98109, United States.

Department of Pathobiology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.

出版信息

ACS Infect Dis. 2021 May 14;7(5):1275-1282. doi: 10.1021/acsinfecdis.1c00076. Epub 2021 Mar 19.

Abstract

New drugs are critically needed to treat infections, particularly for malnourished children under 2 years old in the developing world and persons with immunodeficiencies. Bioactive compounds from the Tres-Cantos GSK library that have activity against other pathogens were screened for possible repurposing against growth. Nineteen compounds grouped into nine structural clusters were identified using an iterative process to remove excessively toxic compounds and screen related compounds from the Tres-Cantos GSK library. Representatives of four different clusters were advanced to a mouse model of infection, but only one compound, an imidazole-pyrimidine, led to significant clearance of infection. This imidazole-pyrimidine compound had a number of favorable safety and pharmacokinetic properties and was maximally active in the mouse model down to 30 mg/kg given daily. Though the mechanism of action against was not definitively established, this imidazole-pyrimidine compound inhibits the known drug target, calcium-dependent protein kinase 1, with a 50% inhibitory concentration of 2 nM. This compound, and related imidazole-pyrimidine molecules, should be further examined as potential leads for therapeutics.

摘要

新的药物对于治疗感染至关重要,特别是在发展中国家营养不足的 2 岁以下儿童和免疫功能低下的人群中。我们筛选了 Tres-Cantos GSK 文库中对其他病原体具有活性的生物活性化合物,以寻找可能对抗 生长的再利用方法。使用迭代过程来去除毒性过大的化合物,并从 Tres-Cantos GSK 文库中筛选相关化合物,确定了 19 种化合物,它们分为 9 个结构簇。代表四个不同簇的化合物被推进到 感染的小鼠模型中,但只有一种化合物,即咪唑嘧啶,导致感染显著清除。这种咪唑嘧啶化合物具有许多良好的安全性和药代动力学特性,在小鼠模型中每天给予 30 毫克/千克时活性最大。尽管针对 的作用机制尚未明确,但这种咪唑嘧啶化合物抑制了已知的 药物靶点,钙依赖性蛋白激酶 1,其 50%抑制浓度为 2 纳摩尔。这种化合物和相关的咪唑嘧啶分子应进一步作为 治疗的潜在先导化合物进行研究。

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