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对具有抗旋毛虫活性的选定化合物的发现的看法——接下来该怎么办?

A perspective on the discovery of selected compounds with anthelmintic activity against the barber's pole worm-Where to from here?

机构信息

Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC, Australia.

Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC, Australia; Faculty of Science and Technology, Federation University, Ballarat, VIC, Australia.

出版信息

Adv Parasitol. 2020;108:1-45. doi: 10.1016/bs.apar.2019.12.003. Epub 2020 Mar 4.

Abstract

Parasitic roundworms (nematodes) cause substantial morbidity and mortality in animals worldwide. Anthelmintic treatment is central to controlling these worms, but widespread resistance to most of the commercially available anthelmintics for veterinary and agricultural use is compromising control, such that there is an urgency to discover new and effective drugs. The purpose of this article is to review information on parasitic nematodes, the treatment and control of parasitic nematode infections and aspects of discovering new anthelmintics in the context of anthelmintic resistance problems, and then to discuss some progress that our group has made in identifying selected compounds with activity against nematodes. The focus of our recent work has been on discovering new chemical entities and known drugs with anthelmintic activities against Haemonchus contortus as well as other socioeconomically important parasitic nematodes for subsequent development. Using whole worm-based phenotypic assays, we have been screening compound collections obtained via product-development-partnerships and/or collaborators, and active compounds have been assessed for their potential as anthelmintic candidates. Following the screening of 15,333 chemicals from five distinct compound collections against H. contortus, we have discovered one new chemical entity (designated SN00797439), two human kinase inhibitors (SNS-032 and AG-1295), 14 tetrahydroquinoxaline analogues, one insecticide (tolfenpyrad) and two tolfenpyrad (pyrazole-5-carboxamide) derivatives (a-15 and a-17) with anthelmintic activity in vitro. Some of these 20 'hit' compounds have selectivity against H. contortus in vitro when compared to particular human cell lines. In our opinion, some of these compounds could represent starting points for 'lead' development. Accordingly, the next research steps to be pursued include: (i) chemical optimisation of representative chemicals via structure-activity relationship (SAR) evaluations; (ii) assessment of the breadth of spectrum of anthelmintic activity on a range of other parasitic nematodes, such as strongyloids, ascaridoids, enoplids and filarioids; (iii) detailed investigations of the absorption, distribution, metabolism, excretion and toxicity (ADMET) of optimised chemicals with broad nematocidal or nematostatic activity; and (iv) establishment of the modes of action of lead candidates.

摘要

寄生虫性圆线虫(线虫)在全球范围内给动物造成了大量的发病率和死亡率。驱虫治疗是控制这些线虫的核心,但兽医和农业用的大多数市售驱虫剂广泛耐药,这使得控制变得复杂,因此迫切需要发现新的有效药物。本文旨在综述寄生虫性线虫的相关信息,以及寄生虫性线虫感染的治疗和控制方法,同时还讨论了在驱虫剂耐药问题背景下发现新驱虫剂的一些进展,然后探讨了我们小组在鉴定具有抗线虫活性的选定化合物方面取得的一些进展。我们最近的工作重点是发现具有驱虫活性的新化学实体和已知药物,以针对旋毛虫以及其他具有社会经济重要性的寄生虫性线虫进行后续开发。我们使用基于全虫的表型测定法,筛选了通过产品开发伙伴关系和/或合作者获得的化合物库,评估了活性化合物作为驱虫候选药物的潜力。在对五个不同化合物库中的 15333 种化学物质进行旋毛虫筛选后,我们发现了一种新的化学实体(命名为 SN00797439)、两种人类激酶抑制剂(SNS-032 和 AG-1295)、14 种四氢喹喔啉类似物、一种杀虫剂(tolfenpyrad)和两种tolfenpyrad(吡唑-5-甲酰胺)衍生物(a-15 和 a-17)具有体外驱虫活性。与特定的人类细胞系相比,这些 20 种“命中”化合物中的一些在体外对旋毛虫具有选择性。在我们看来,其中一些化合物可能是“先导”开发的起点。因此,下一步的研究步骤包括:(i)通过结构-活性关系(SAR)评估对代表性化合物进行化学优化;(ii)评估一系列其他寄生虫性线虫(如Strongyloides、Ascaridoids、Enoplids 和 Filarioids)的广谱驱虫活性;(iii)详细研究具有广泛杀线虫或线虫静止活性的优化化合物的吸收、分布、代谢、排泄和毒性(ADMET);(iv)建立先导候选药物的作用模式。

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