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https://hdl.handle.net/10495/32004
Título : | Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration |
Autor : | Pabón Vidal, Adriana Lucía Quiliano, Miguel Mendoza, Adela Fong, Kim Goldfarb, Nathan Fabing, Isabelle Vettorazzi, Ariane López de Cerain, Adela Dunn, Ben Garavito, Giovanny Wright, David DeHaro, Eric Pérez Silanes, Silvia Aldana, Ignacio Galiano, Silvia |
metadata.dc.subject.*: | Drug-Related Side Effects and Adverse Reactions Antimaláricos Antimalarials Amino Alcoholes Amino Alcohols Modelos Animales de Enfermedad Disease Models, Animal Concentración 50 Inhibidora Inhibitory Concentration 50 Malaria Falciparum Malaria, Falciparum Plasmodium falciparum Relación Estructura-Actividad Structure-Activity Relationship Resultado del Tratamiento Treatment Outcome Análisis de Supervivencia Survival Analysis Ratones Mice http://id.nlm.nih.gov/mesh/D064420 |
Fecha de publicación : | 2016 |
Editorial : | Elsevier |
Citación : | Quiliano M, Mendoza A, Fong KY, Pabón A, Goldfarb NE, Fabing I, Vettorazzi A, López de Cerain A, Dunn BM, Garavito G, Wright DW, Deharo E, Pérez-Silanes S, Aldana I, Galiano S. Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration. Int J Parasitol Drugs Drug Resist. 2016 Dec;6(3):184-198. doi: 10.1016/j.ijpddr.2016.09.004. |
Resumen : | ABSTRACT: Synthesis of new 1-aryl-3-substituted propanol derivatives followed by structure-activity relationship, in silico drug-likeness, cytotoxicity, genotoxicity, in silico metabolism, in silico pharmacophore modeling, and in vivo studies led to the identification of compounds 22 and 23 with significant in vitro antiplasmodial activity against drug sensitive (D6 IC50 ≤ 0.19 μM) and multidrug resistant (FCR-3 IC50 ≤ 0.40 μM and C235 IC50 ≤ 0.28 μM) strains of Plasmodium falciparum. Adequate selectivity index and absence of genotoxicity was also observed. Notably, compound 22 displays excellent parasitemia reduction (98 ± 1%), and complete cure with all treated mice surviving through the entire period with no signs of toxicity. One important factor is the agreement between in vitro potency and in vivo studies. Target exploration was performed; this chemotype series exhibits an alternative antimalarial mechanism. |
ISSN : | 2211-3207 |
metadata.dc.identifier.doi: | 10.1016/j.ijpddr.2016.09.004 |
Aparece en las colecciones: | Artículos de Revista en Ciencias Médicas |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
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PabonAdriana_2016_ExploringAntimalarialEvaluation.pdf | Artículo de investigación | 1.72 MB | Adobe PDF | Visualizar/Abrir |
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