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
{"title":"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","authors":"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","doi":"10.1016/j.ijpddr.2024.100522","DOIUrl":null,"url":null,"abstract":"<div><p>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 <em>Caenorhabditis elegans</em>; and predicted compound-target relationships by thermal proteome profiling (TPP) and <em>in silico</em> docking. Here, we logically extended this work and critically evaluated the anthelmintic activity of ABX464 analogues on <em>Haemonchus contortus</em> (barber's pole worm) – a highly pathogenic nematode of ruminant livestock. First, we tested a series of 44 analogues on <em>H. contortus</em> (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 <em>Ancylostoma, Heligmosomoides</em> and <em>Strongyloides</em> species). Using TPP and <em>in silico</em> modelling studies, we predicted protein HCON_00074590 (a predicted aldo-keto reductase) as a target candidate for ABX464 in <em>H. contortus</em>. 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.</p></div>","PeriodicalId":13775,"journal":{"name":"International Journal for Parasitology: Drugs and Drug Resistance","volume":"24 ","pages":"Article 100522"},"PeriodicalIF":4.1000,"publicationDate":"2024-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211320724000034/pdfft?md5=256699c4f264c5754a968fc968bc1efd&pid=1-s2.0-S2211320724000034-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Structure-activity relationship and target investigation of 2-aryl quinolines with nematocidal activity\",\"authors\":\"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\",\"doi\":\"10.1016/j.ijpddr.2024.100522\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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 <em>Caenorhabditis elegans</em>; and predicted compound-target relationships by thermal proteome profiling (TPP) and <em>in silico</em> docking. Here, we logically extended this work and critically evaluated the anthelmintic activity of ABX464 analogues on <em>Haemonchus contortus</em> (barber's pole worm) – a highly pathogenic nematode of ruminant livestock. First, we tested a series of 44 analogues on <em>H. contortus</em> (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 <em>Ancylostoma, Heligmosomoides</em> and <em>Strongyloides</em> species). Using TPP and <em>in silico</em> modelling studies, we predicted protein HCON_00074590 (a predicted aldo-keto reductase) as a target candidate for ABX464 in <em>H. contortus</em>. 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.</p></div>\",\"PeriodicalId\":13775,\"journal\":{\"name\":\"International Journal for Parasitology: Drugs and Drug Resistance\",\"volume\":\"24 \",\"pages\":\"Article 100522\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2024-01-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2211320724000034/pdfft?md5=256699c4f264c5754a968fc968bc1efd&pid=1-s2.0-S2211320724000034-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal for Parasitology: Drugs and Drug Resistance\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2211320724000034\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PARASITOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal for Parasitology: Drugs and Drug Resistance","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211320724000034","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PARASITOLOGY","Score":null,"Total":0}
Structure-activity relationship and target investigation of 2-aryl quinolines with nematocidal activity
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.
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.