Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/1741
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dc.contributor.authorBúa, Jacquelinees
dc.contributor.authorRuiz, Andrés Mes
dc.contributor.authorPotenza, Marianaes
dc.contributor.authorFichera, Laura Ees
dc.date.accessioned2020-11-25T21:46:27Z-
dc.date.available2020-11-25T21:46:27Z-
dc.date.issued2004-09-20-
dc.identifier.issn0960-894X-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/1741-
dc.descriptionFil: Búa, Jacqueline. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Parasitología. Consejo Nacional de Investigaciones, Científicas y Técnicas; Argentina.es
dc.description.abstractCyclosporin A (CsA) nonimmunosuppressive analogs were evaluated against Trypanosoma cruzi and on TcCyP19, a cyclophilin of 19 kDa. Two out of eight CsA analogs, H-7-94 and F-7-62 showed the best anti-parasitic effects on all in vitro assays. Their IC(50) values were 0.82 and 3.41 microM, respectively, compared to CsA IC(50) value 5.39 microM on epimastigote proliferation; and on trypomastigote lysis their IC(50) values were 0.97 and 2.66 microM compared to CsA IC(50) value 7.19 microM. H-7-94 and F-7-62 were also more effective than CsA in inhibiting trypomastigote infection. The enzymatic activity of TcCyP19 was inhibited by all CsA derivatives, suggesting this target is involved in the trypanocidal effects observed.es
dc.formatpdf-
dc.language.isoenes
dc.relation.ispartofBioorganic & medicinal chemistry letterses
dc.rightsOpen Access-
dc.rightsCreative Commons Attribution 4.0 International License-
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.sourceBioorganic & Medicinal Chemistry Letters 2004;14:4633-4637.-
dc.subjectAnimaleses
dc.subjectChlorocebus aethiopses
dc.subjectCiclofilinases
dc.subjectCiclosporinases
dc.subjectInmunosupresoreses
dc.subjectRelación Estructura-Actividades
dc.subjectTripanocidases
dc.subjectTrypanosoma cruzies
dc.subjectCélulas Veroes
dc.titleIn vitro anti-parasitic activity of Cyclosporin A analogs on Trypanosoma cruzies
dc.typeArtículoes
dc.identifier.doi10.1016/j.bmcl.2004.07.003-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.openairetypeArtículo-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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