{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,2]],"date-time":"2026-07-02T08:06:22Z","timestamp":1782979582484,"version":"3.54.5"},"update-to":[{"DOI":"10.1371\/journal.pntd.0012050","type":"new_version","label":"New version","source":"publisher","updated":{"date-parts":[[2024,4,4]],"date-time":"2024-04-04T00:00:00Z","timestamp":1712188800000}}],"reference-count":71,"publisher":"Public Library of Science (PLoS)","issue":"3","license":[{"start":{"date-parts":[[2024,3,25]],"date-time":"2024-03-25T00:00:00Z","timestamp":1711324800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100001823","name":"Ministerstvo \u0160kolstv\u00ed, Ml\u00e1de\u017ee a T\u011blov\u00fdchovy","doi-asserted-by":"publisher","award":["OP JAC CZ.02.01.01\/00\/22_010\/0002902 MSCA Fellowships CZ - UK"],"award-info":[{"award-number":["OP JAC CZ.02.01.01\/00\/22_010\/0002902 MSCA Fellowships CZ - UK"]}],"id":[{"id":"10.13039\/501100001823","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001843","name":"Science and Engineering Research Board","doi-asserted-by":"publisher","award":["CRG\/2020\/005800"],"award-info":[{"award-number":["CRG\/2020\/005800"]}],"id":[{"id":"10.13039\/501100001843","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["www.plosntds.org"],"crossmark-restriction":false},"short-container-title":["PLoS Negl Trop Dis"],"abstract":"<jats:p>Pharmacophores such as hydroxyethylamine (HEA) and phthalimide (PHT) have been identified as potential synthons for the development of compounds against various parasitic infections. In order to further advance our progress, we conducted an experiment utilising a collection of PHT and HEA derivatives through phenotypic screening against a diverse set of protist parasites. This approach led to the identification of a number of compounds that exhibited significant effects on the survival of <jats:italic>Entamoeba histolytica<\/jats:italic>, <jats:italic>Trypanosoma brucei<\/jats:italic>, and multiple life-cycle stages of <jats:italic>Leishmania spp<\/jats:italic>. The <jats:italic>Leishmania<\/jats:italic> hits were pursued due to the pressing necessity to expand our repertoire of reliable, cost-effective, and efficient medications for the treatment of leishmaniases. Antileishmanials must possess the essential capability to efficiently penetrate the host cells and their compartments in the disease context, to effectively eliminate the intracellular parasite. Hence, we performed a study to assess the effectiveness of eradicating <jats:italic>L<\/jats:italic>. <jats:italic>infantum<\/jats:italic> intracellular amastigotes in a model of macrophage infection. Among eleven <jats:italic>L<\/jats:italic>. <jats:italic>infantum<\/jats:italic> growth inhibitors with low-micromolar potency, PHT-39, which carries a trifluoromethyl substitution, demonstrated the highest efficacy in the intramacrophage assay, with an EC50 of 1.2 +\/- 3.2 \u03bcM. Cytotoxicity testing of PHT-39 in HepG2 cells indicated a promising selectivity of over 90-fold. A chemogenomic profiling approach was conducted using an orthology-based method to elucidate the mode of action of PHT-39. This genome-wide RNA interference library of <jats:italic>T<\/jats:italic>. <jats:italic>brucei<\/jats:italic> identified sensitivity determinants for PHT-39, which included a P-type ATPase that is crucial for the uptake of miltefosine and amphotericin, strongly indicating a shared route for cellular entry. Notwithstanding the favourable properties and demonstrated efficacy in the <jats:italic>Plasmodium berghei<\/jats:italic> infection model, PHT-39 was unable to eradicate <jats:italic>L<\/jats:italic>. <jats:italic>major<\/jats:italic> infection in a murine infection model of cutaneous leishmaniasis. Currently, PHT-39 is undergoing derivatization to optimize its pharmacological characteristics.<\/jats:p>","DOI":"10.1371\/journal.pntd.0012050","type":"journal-article","created":{"date-parts":[[2024,3,25]],"date-time":"2024-03-25T17:45:07Z","timestamp":1711388707000},"page":"e0012050","update-policy":"https:\/\/doi.org\/10.1371\/journal.pntd.corrections_policy","source":"Crossref","is-referenced-by-count":8,"title":["Phenotypic screening reveals a highly selective phthalimide-based compound with antileishmanial 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