Antiviral activity of sertindole, raloxifene and ibutamoren against transcription and replication-competent Ebola virus-like particles

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dc.contributor.authorYoon, Yi-Seulko
dc.contributor.authorJang, Yejinko
dc.contributor.authorHoenen, Thomasko
dc.contributor.authorShin, Heegwonko
dc.contributor.authorLee, Younghoonko
dc.contributor.authorKim, Meehyeinko
dc.date.accessioned2020-05-28T07:20:05Z-
dc.date.available2020-05-28T07:20:05Z-
dc.date.created2020-05-25-
dc.date.created2020-05-25-
dc.date.issued2020-03-
dc.identifier.citationBMB REPORTS, v.53, no.3, pp.166 - 171-
dc.identifier.issn1976-6696-
dc.identifier.urihttp://hdl.handle.net/10203/274337-
dc.description.abstractA chemical library comprising 2,354 drug-like compounds was screened using a transcription and replication-competent virus-like particle (trVLP) system implementing the whole Ebola virus (EBOV) life cycle. Dose-dependent inhibition of Ebola trVLP replication was induced by 15 hit compounds, which primarily target different types of G protein-coupled receptors (GPCRs). Based on the chemical structure, the compounds were divided into three groups, diphenylmethane derivatives, promazine derivatives and chemicals with no conserved skeletons. The third group included sertindole, raloxifene, and ibutamoren showing prominent antiviral effects in cells. They downregulated the expression of viral proteins, including the VP40 matrix protein and the envelope glycoprotein. They also reduced the amount of EBOV-derived tetracistronic minige-nome RNA incorporated into progeny trVLPs in the culture supernatant Particularly, ibutamoren, which is a known agonist of growth hormone secretagogue receptor (GHSR), showed the most promising antiviral activity with a 50% effective concentration of 0.2 mu M, a 50% cytotoxic concentration of 42.4 mu M, and a selectivity index of 222.8. Here, we suggest a strategy for development of anti-EBOV therapeutics by adopting GHSR agonists as hit compounds.-
dc.languageEnglish-
dc.publisherKOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY-
dc.titleAntiviral activity of sertindole, raloxifene and ibutamoren against transcription and replication-competent Ebola virus-like particles-
dc.typeArticle-
dc.identifier.wosid000531499200007-
dc.identifier.scopusid2-s2.0-85082560991-
dc.type.rimsART-
dc.citation.volume53-
dc.citation.issue3-
dc.citation.beginningpage166-
dc.citation.endingpage171-
dc.citation.publicationnameBMB REPORTS-
dc.identifier.doi10.5483/BMBRep.2020.53.3.175-
dc.identifier.kciidART002571313-
dc.contributor.localauthorLee, Younghoon-
dc.contributor.nonIdAuthorYoon, Yi-Seul-
dc.contributor.nonIdAuthorJang, Yejin-
dc.contributor.nonIdAuthorHoenen, Thomas-
dc.contributor.nonIdAuthorKim, Meehyein-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorAntiviral-
dc.subject.keywordAuthorEbola virus-
dc.subject.keywordAuthorIbutamoren-
dc.subject.keywordAuthorRaloxifene-
dc.subject.keywordAuthorSertindole-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusENTRY-
dc.subject.keywordPlusMINIGENOME-
dc.subject.keywordPlusSYSTEM-
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