Structure-activity relationship and target investigation of 2-aryl quinolines with nematocidal activity

Harrison T. Shanley , Aya C. Taki , Nghi Nguyen , Tao Wang , Joseph J. Byrne , Ching-Seng Ang , Michael G. Leeming , Shuai Nie , Nicholas Williamson , Yuanting Zheng , Neil D. Young , Pasi K. Korhonen , Andreas Hofmann , Bill C.H. Chang , Tim N.C. Wells , Cécile Häberli , Jennifer Keiser , Abdul Jabbar , Brad E. Sleebs , Robin B. Gasser
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Abstract

Within the context of our anthelmintic discovery program, we recently identified and evaluated a quinoline derivative, called ABX464 or obefazimod, as a nematocidal candidate; synthesised a series of analogues which were assessed for activity against the free-living nematode Caenorhabditis elegans; and predicted compound-target relationships by thermal proteome profiling (TPP) and in silico docking. Here, we logically extended this work and critically evaluated the anthelmintic activity of ABX464 analogues on Haemonchus contortus (barber's pole worm) – a highly pathogenic nematode of ruminant livestock. First, we tested a series of 44 analogues on H. contortus (larvae and adults) to investigate the nematocidal pharmacophore of ABX464, and identified one compound with greater potency than the parent compound and showed moderate activity against a select number of other parasitic nematodes (including Ancylostoma, Heligmosomoides and Strongyloides species). Using TPP and in silico modelling studies, we predicted protein HCON_00074590 (a predicted aldo-keto reductase) as a target candidate for ABX464 in H. contortus. Future work aims to optimise this compound as a nematocidal candidate and investigate its pharmacokinetic properties. Overall, this study presents a first step toward the development of a new nematocide.

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具有杀线虫活性的 2-芳基喹啉类化合物的结构-活性关系和目标研究
在我们的驱虫药发现计划中,我们最近发现并评估了一种名为 ABX464 或 obefazimod 的喹啉衍生物,将其作为一种杀线虫候选药物;合成了一系列类似物,并评估了这些类似物对自由生活线虫 Caenorhabditis elegans 的活性;还通过热蛋白质组图谱分析 (TPP) 和硅对接预测了化合物与靶标的关系。在这里,我们顺理成章地扩展了这项工作,并严格评估了 ABX464 类似物对反刍家畜的高致病性线虫--柯氏萦线虫(理发师杆线虫)的驱虫活性。首先,我们对一系列 44 种类似物进行了测试,以研究 ABX464 的杀线虫药效,结果发现一种化合物比母体化合物具有更强的药效,并且对一些其他寄生线虫(包括安氏线虫、螺旋体线虫和强直线虫)具有中等程度的活性。利用 TPP 和硅学建模研究,我们预测蛋白 HCON_00074590(一种预测的醛酮还原酶)是 ABX464 在 H. contortus 中的候选靶标。未来工作的目标是将该化合物优化为杀线虫候选化合物,并研究其药代动力学特性。总之,这项研究为开发新的杀线虫药物迈出了第一步。
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来源期刊
CiteScore
7.90
自引率
7.50%
发文量
31
审稿时长
48 days
期刊介绍: The International Journal for Parasitology – Drugs and Drug Resistance is one of a series of specialist, open access journals launched by the International Journal for Parasitology. It publishes the results of original research in the area of anti-parasite drug identification, development and evaluation, and parasite drug resistance. The journal also covers research into natural products as anti-parasitic agents, and bioactive parasite products. Studies can be aimed at unicellular or multicellular parasites of human or veterinary importance.
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