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Journal of Medicinal Chemistry|May 8, 2019
Falcipain Inhibitors Based on the Natural Product Gallinamide A Are Potent in Vitro and in Vivo AntimalarialsAlexander Stoye, Annette Juillard, Arthur H Tang, et al.Journal of Medicinal Chemistry|June 8, 2011
Antimalarial pyrido[1,2-a]benzimidazolesAlbert J Ndakala, Richard K Gessner, Patricia W Gitari, et al.Journal of Medicinal Chemistry|August 7, 2015
6-Arylpyrazine-2-carboxamides: A New Core for Trypanosoma brucei InhibitorsRaphaël Rahmani, Kung Ban, Amy J Jones, et al.Bioorganic & Medicinal Chemistry Letters|July 21, 2009
Discovery of CYT997: a structurally novel orally active microtubule targeting agentChristopher J Burns, Michael F Harte, Xianyong Bu, et al.Malaria Journal|February 20, 2021
Selecting an anti-malarial clinical candidate from two potent dihydroisoquinolonesYizhe Chen, Fangyi Zhu, Jared Hammill, et al.Bioorganic & Medicinal Chemistry Letters|February 12, 2008
Characterization of the two major CYP450 metabolites of ozonide (1,2,4-trioxolane) OZ277Lin Zhou, André Alker, Armin Ruf, et al.Bioorganic & Medicinal Chemistry Letters|August 26, 2006
Antimalarial activity of N-alkyl amine, carboxamide, sulfonamide, and urea derivatives of a dispiro-1,2,4-trioxolane piperidineManiyan Padmanilayam, Bernard Scorneaux, Yuxiang Dong, et al.Drug Design, Development and Therapy|November 21, 2013
In vitro and in vivo characterization of the antimalarial lead compound SSJ-183 in Plasmodium modelsSarah Schleiferböck, Christian Scheurer, Masataka Ihara, et al.Scientific Reports|October 18, 2016
Nitroheterocyclic drugs cure experimental Trypanosoma cruzi infections more effectively in the chronic stage than in the acute stageAmanda Fortes Francisco, Shiromani Jayawardhana, Michael D Lewis, et al.Antimicrobial Agents and Chemotherapy|April 8, 2015
Enantiomers of nifurtimox do not exhibit stereoselective anti-Trypanosoma cruzi activity, toxicity, or pharmacokinetic propertiesCarolina B Moraes, Karen L White, Stéphanie Braillard, et al.Pageof 18