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European Journal of Medicinal Chemistry|March 19, 2026
Structure-based design of new pyrazole inhibitors targeting Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH)Agnese C Pippione, Noemi Villella, Federico Fornaseri, et al.RSC Medicinal Chemistry|June 23, 2025
Pharmacophore-guided optimization of the hit compound CTN1122 in the design of promising imidazo[1,2-<i>a</i>]pyrazine derivatives targeting the casein kinase 1 for antileishmanial therapyLhana Tisseur, Cédric Logé, Sandrine Cojean, et al.Research Square|July 29, 2024
Ex vivo susceptibility to antimalarial drugs and polymorphisms in drug resistance genes of African Plasmodium falciparum, 2016-2023: a genotype-phenotype association studyJason Rosado, Abebe A Fola, Sandrine Cojean, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|April 18, 2025
Re-sensitization of antimony-resistant Leishmania by highly potent Sb<sup>V</sup>-porphyrin through the involvement of ERG6-coding geneEllen Gonçalves de Oliveira, Juliane Sousa Lanza, Sandrine Cojean, et al.Scientific Reports|November 16, 2017
ABMA, a small molecule that inhibits intracellular toxins and pathogens by interfering with late endosomal compartmentsYu Wu, Valérie Pons, Amélie Goudet, et al.Chemico-Biological Interactions|October 8, 2016
Inhibitors of retrograde trafficking active against ricin and Shiga toxins also protect cells from several viruses, Leishmania and ChlamydialesNeetu Gupta, Romain Noël, Amélie Goudet, et al.Pageof 6