dc.creatorAlberca, Lucas Nicolás
dc.creatorChuguransky, Sara Rocío
dc.creatorÁlvarez, Cora L.
dc.creatorTalevi, Alan
dc.creatorSalas Sarduy, Emir
dc.date2019
dc.date2020-10-28T18:16:32Z
dc.date.accessioned2023-07-14T22:44:54Z
dc.date.available2023-07-14T22:44:54Z
dc.identifierhttp://sedici.unlp.edu.ar/handle/10915/107892
dc.identifierhttp://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC6691349&blobtype=pdf
dc.identifierissn:2296-2646
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/7448055
dc.descriptionMalaria is among the leading causes of death worldwide. The emergence of <i>Plasmodium falciparum</i> resistant strains with reduced sensitivity to the first line combination therapy and suboptimal responses to insecticides used for Anopheles vector management have led to renewed interest in novel therapeutic options. Here, we report the development and validation of an ensemble of ligand-based computational models capable of identifying falcipain-2 inhibitors, and their subsequent application in the virtual screening of DrugBank and Sweetlead libraries. Among four hits submitted to enzymatic assays, two (odanacatib, an abandoned investigational treatment for osteoporosis and bone metastasis, and the antibiotic methacycline) confirmed inhibitory effects on falcipain-2, with Ki of 98.2 nM and 84.4µM. Interestingly, Methacycline proved to be a non-competitive inhibitor (α = 1.42) of falcipain-2. The effects of both hits on falcipain-2 hemoglobinase activity and on the development of <i>P. falciparum</i> were also studied.
dc.descriptionLaboratorio de Investigación y Desarrollo de Bioactivos
dc.formatapplication/pdf
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by/4.0/
dc.rightsCreative Commons Attribution 4.0 International (CC BY 4.0)
dc.subjectCiencias Exactas
dc.subjectMalaria
dc.subjectPlasmodium falciparum
dc.subjectFalcipain-2
dc.subjectDrug repositioning
dc.subjectVirtual screening
dc.subjectDrug rescue
dc.subjectOdanacatib
dc.subjectMethacycline
dc.titleIn <i>silico</i> Guided Drug Repurposing : Discovery of New Competitive and Non-competitive Inhibitors of Falcipain-2
dc.typeArticulo
dc.typeArticulo


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