Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/103190
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dc.contributor.authorPavao Guerra-Slompo, Eloise-
dc.contributor.authorPicchi-Constante, Gisele Fernanda Assine-
dc.contributor.authorMarek, Martin-
dc.contributor.authorRomier, Christophe-
dc.contributor.authorSippl, Wolfgang-
dc.contributor.authorZanchin, Nilson Ivo Tonin-
dc.date.accessioned2023-05-08T07:41:53Z-
dc.date.available2023-05-08T07:41:53Z-
dc.date.issued2023-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/105142-
dc.identifier.urihttp://dx.doi.org/10.25673/103190-
dc.description.abstractHere, we describe a combined in cellulo and in vivo approach to identify compounds with higher potential for efficient inhibition of Trypanosoma cruzi. Phase I of in cellulo assays is designed to exclude inactive or toxic compounds, while phase II is designed for accurate IC50, CC50, and selective index (SI) determination. Compounds showing high SI are tested using in vivo infection models in parallel with benznidazole to assess their efficacy relative to a reference drug used for Chagas disease treatment.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subject.ddc615-
dc.titleIn cellulo and in vivo assays for compound testing against Trypanosoma cruzieng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleSTAR Protocols-
local.bibliographicCitation.volume4-
local.bibliographicCitation.issue1-
local.bibliographicCitation.publishernameCell Press-
local.bibliographicCitation.publisherplaceCambridge, MA-
local.bibliographicCitation.doi10.1016/j.xpro.2023.102058-
local.openaccesstrue-
dc.identifier.ppn1844753026-
local.bibliographicCitation.year2023-
cbs.sru.importDate2023-05-08T07:41:24Z-
local.bibliographicCitationEnthalten in STAR Protocols - Cambridge, MA : Cell Press, 2020-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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