Zeeman Anne-Marie, Vermaat Lars, Castellote Alvaro M Isabel, Van der Werff Nicole M, Glas-Nieuwenhuis Ivonne G, Harupa-Chung Anke, Calderón Félix, Gamo Fransisco-Javier, Fernandez Alvaro Elena, Kocken Clemens H M
Department of Parasitology, Biomedical Primate Research Centre, Rijswijk, The Netherlands.
Global Health Medicines R&D, GSK, Madrid, Spain.
Antimicrob Agents Chemother. 2025 Aug 6;69(8):e0181224. doi: 10.1128/aac.01812-24. Epub 2025 Jul 17.
This study aimed to identify new compounds with prophylactic activity against liver stages, particularly hypnozoites. A small, focused set of 568 compounds from the GSK open-access TCAMS library was tested against liver stages. Among these compounds, 12 showed IC values below 2 µM against hypnozoites, with the most active compound displaying nanomolar activity. These active compounds could be assigned to/grouped into six chemical clusters. Some compounds could be associated with potential known modes of action such as cytochrome bc1 inhibition or kinase inhibition, whereas the mode of action of other hit compounds is currently unknown. The high hit rate in this screening may be attributed to preselecting compounds based on their activity against gametocytes and liver stages in other species. Based on our findings, we suggest that this preselection methodology is appropriate for finding compounds that are active against hypnozoites.
本研究旨在鉴定对肝期,特别是对休眠子具有预防活性的新化合物。从葛兰素史克(GSK)开放获取的TCAMS库中选取了一组规模较小、针对性强的568种化合物,对其进行肝期测试。在这些化合物中,有12种对休眠子的半数抑制浓度(IC)值低于2µM,其中活性最高的化合物表现出纳摩尔级活性。这些活性化合物可分为六个化学簇。一些化合物可能与潜在的已知作用模式有关,如细胞色素bc1抑制或激酶抑制,而其他命中化合物的作用模式目前尚不清楚。此次筛选中的高命中率可能归因于基于化合物对其他物种配子体和肝期的活性进行预筛选。基于我们的研究结果,我们认为这种预筛选方法适用于寻找对休眠子有活性的化合物。