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dc.contributor.authorRuan, B
dc.contributor.authorZhang, Y
dc.contributor.authorTadesse, S
dc.contributor.authorPreston, S
dc.contributor.authorTaki, AC
dc.contributor.authorJabbar, A
dc.contributor.authorHofmann, A
dc.contributor.authorJiao, Y
dc.contributor.authorGarcia-Bustos, J
dc.contributor.authorHarjani, J
dc.contributor.authorLe, TG
dc.contributor.authorVarghese, S
dc.contributor.authorTeguh, S
dc.contributor.authorXie, Y
dc.contributor.authorOdiba, J
dc.contributor.authorHu, M
dc.contributor.authorGasser, RB
dc.contributor.authorBaell, J
dc.date.accessioned2021-01-06T01:46:40Z
dc.date.available2021-01-06T01:46:40Z
dc.date.issued2020-03-15
dc.identifierpii: S0223-5234(20)30067-2
dc.identifier.citationRuan, B., Zhang, Y., Tadesse, S., Preston, S., Taki, A. C., Jabbar, A., Hofmann, A., Jiao, Y., Garcia-Bustos, J., Harjani, J., Le, T. G., Varghese, S., Teguh, S., Xie, Y., Odiba, J., Hu, M., Gasser, R. B. & Baell, J. (2020). Synthesis and structure-activity relationship study of pyrrolidine-oxadiazoles as anthelmintics against Haemonchus contortus. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 190, https://doi.org/10.1016/j.ejmech.2020.112100.
dc.identifier.issn0223-5234
dc.identifier.urihttp://hdl.handle.net/11343/258577
dc.description.abstractParasitic roundworms (nematodes) are significant pathogens of humans and animals and cause substantive socioeconomic losses due to the diseases that they cause. The control of nematodes in livestock animals relies heavily on the use of anthelmintic drugs. However, their extensive use has led to a widespread problem of drug resistance in these worms. Thus, the discovery and development of novel chemical entities for the treatment of parasitic worms of humans and animals is needed. Herein, we describe our medicinal chemistry optimization efforts of a phenotypic hit against Haemonchus contortus based on a pyrrolidine-oxadiazole scaffold. This led to the identification of compounds with potent inhibitory activities (IC50 = 0.78-22.4 μM) on the motility and development of parasitic stages of H. contortus, and which were found to be highly selective in a mammalian cell counter-screen. These compounds could be used as suitable chemical tools for drug target identification or as lead compounds for further optimization.
dc.languageEnglish
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
dc.titleSynthesis and structure-activity relationship study of pyrrolidine-oxadiazoles as anthelmintics against Haemonchus contortus
dc.typeJournal Article
dc.identifier.doi10.1016/j.ejmech.2020.112100
melbourne.affiliation.departmentVeterinary Biosciences
melbourne.source.titleEuropean Journal of Medicinal Chemistry
melbourne.source.volume190
melbourne.identifier.nhmrc1102322
melbourne.identifier.arcLP160100058
melbourne.elementsid1432225
melbourne.contributor.authorTaki, Aya
melbourne.contributor.authorGarcia-Bustos, Jose
melbourne.contributor.authorJabbar, Abdul
melbourne.contributor.authorGasser, Robin
melbourne.contributor.authorHofmann, Andreas
dc.identifier.eissn1768-3254
melbourne.identifier.fundernameidNHMRC, 1102322
melbourne.identifier.fundernameidAustralian Research Council, LP160100058
melbourne.accessrightsThis item is currently not available from this repository


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