{"title":"利用基于红外的秀丽隐杆线虫运动性检测方法,在疟疾药物创投公司的COVID和全球卫生优先箱中发现具有驱虫潜力的小分子。","authors":"Yujie Uli Sun, Lawrence J Liu, Conor R Caffrey","doi":"10.1186/s13104-025-07485-9","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Parasitic nematodes are a public health problem globally, and an economic burden on animal and plant agricultural industries. With their ability to generate drug resistance, new anthelmintic compounds must be constantly sourced.</p><p><strong>Methods: </strong>Using the free-living nematode, Caenorhabditis elegans, in an infrared-based motility assay, we screened 400 compounds from two open-source, small-molecule collections distributed by the Medicines for Malaria Venture, namely, the COVID Box and Global Health Priority Box. The screening assay was first validated for worm number, DMSO concentration and final volume.</p><p><strong>Results: </strong>Primary and secondary (time- and concentration-dependent) screens of both boxes, identified twelve compounds as hits; nine of which are known anthelmintics. Three additional bioactives, flufenerim, flucofuron and indomethacin were identified with EC<sub>50</sub> values ranging from 0.211 to 23.174 µM. Counter toxicity screens with HEK293 cells indicated varying degrees of toxicity with EC<sub>50</sub> values ranging from 0.453 to > 100 µM.</p><p><strong>Conclusions: </strong>A C. elegans motility assay was optimized and used to screen two recently-released, small molecule libraries. Flufenerim, flucofuron and/or indomethacin might serve as starting points for the development of new anthelmintics.</p>","PeriodicalId":9234,"journal":{"name":"BMC Research Notes","volume":"18 1","pages":"422"},"PeriodicalIF":1.7000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Discovery of small molecules with anthelmintic potential in the Medicines for Malaria Venture's COVID and Global Health Priority Boxes using an infrared-based assay for Caenorhabditis elegans motility.\",\"authors\":\"Yujie Uli Sun, Lawrence J Liu, Conor R Caffrey\",\"doi\":\"10.1186/s13104-025-07485-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Parasitic nematodes are a public health problem globally, and an economic burden on animal and plant agricultural industries. With their ability to generate drug resistance, new anthelmintic compounds must be constantly sourced.</p><p><strong>Methods: </strong>Using the free-living nematode, Caenorhabditis elegans, in an infrared-based motility assay, we screened 400 compounds from two open-source, small-molecule collections distributed by the Medicines for Malaria Venture, namely, the COVID Box and Global Health Priority Box. The screening assay was first validated for worm number, DMSO concentration and final volume.</p><p><strong>Results: </strong>Primary and secondary (time- and concentration-dependent) screens of both boxes, identified twelve compounds as hits; nine of which are known anthelmintics. Three additional bioactives, flufenerim, flucofuron and indomethacin were identified with EC<sub>50</sub> values ranging from 0.211 to 23.174 µM. Counter toxicity screens with HEK293 cells indicated varying degrees of toxicity with EC<sub>50</sub> values ranging from 0.453 to > 100 µM.</p><p><strong>Conclusions: </strong>A C. elegans motility assay was optimized and used to screen two recently-released, small molecule libraries. Flufenerim, flucofuron and/or indomethacin might serve as starting points for the development of new anthelmintics.</p>\",\"PeriodicalId\":9234,\"journal\":{\"name\":\"BMC Research Notes\",\"volume\":\"18 1\",\"pages\":\"422\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-10-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Research Notes\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1186/s13104-025-07485-9\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Research Notes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s13104-025-07485-9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
背景:寄生虫是全球性的公共卫生问题,也是动植物农业的经济负担。由于它们具有产生耐药性的能力,必须不断寻找新的驱虫药化合物。方法:利用自由生活的线虫秀丽隐杆线虫(Caenorhabditis elegans)进行红外运动试验,从疟疾药物项目(Medicines for Malaria Venture)分发的两个开源小分子收集品(即COVID Box和Global Health Priority Box)中筛选400种化合物。筛选实验首先验证了蠕虫数量、DMSO浓度和最终体积。结果:两个盒子的一级和二级(时间和浓度依赖)筛选鉴定出12种化合物为命中;其中九种是已知的驱虫药。另外三种生物活性物质氟非那宁、氟呋隆和吲哚美辛的EC50值在0.211 ~ 23.174µM之间。HEK293细胞的反毒性筛选显示不同程度的毒性,EC50值在0.453至bbb100µM之间。结论:优化了秀丽隐杆线虫运动检测方法,并用于筛选两个新发布的小分子文库。氟非那宁、氟氟呋喃和/或吲哚美辛可作为开发新的驱虫剂的起点。
Discovery of small molecules with anthelmintic potential in the Medicines for Malaria Venture's COVID and Global Health Priority Boxes using an infrared-based assay for Caenorhabditis elegans motility.
Background: Parasitic nematodes are a public health problem globally, and an economic burden on animal and plant agricultural industries. With their ability to generate drug resistance, new anthelmintic compounds must be constantly sourced.
Methods: Using the free-living nematode, Caenorhabditis elegans, in an infrared-based motility assay, we screened 400 compounds from two open-source, small-molecule collections distributed by the Medicines for Malaria Venture, namely, the COVID Box and Global Health Priority Box. The screening assay was first validated for worm number, DMSO concentration and final volume.
Results: Primary and secondary (time- and concentration-dependent) screens of both boxes, identified twelve compounds as hits; nine of which are known anthelmintics. Three additional bioactives, flufenerim, flucofuron and indomethacin were identified with EC50 values ranging from 0.211 to 23.174 µM. Counter toxicity screens with HEK293 cells indicated varying degrees of toxicity with EC50 values ranging from 0.453 to > 100 µM.
Conclusions: A C. elegans motility assay was optimized and used to screen two recently-released, small molecule libraries. Flufenerim, flucofuron and/or indomethacin might serve as starting points for the development of new anthelmintics.
BMC Research NotesBiochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
3.60
自引率
0.00%
发文量
363
审稿时长
15 weeks
期刊介绍:
BMC Research Notes publishes scientifically valid research outputs that cannot be considered as full research or methodology articles. We support the research community across all scientific and clinical disciplines by providing an open access forum for sharing data and useful information; this includes, but is not limited to, updates to previous work, additions to established methods, short publications, null results, research proposals and data management plans.