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ACS Omega|May 27, 2024
Synthesis and Anti-Trypanosoma cruzi Activity of 3-Cyanopyridine DerivativesBrian W Slafer, Marco A Dessoy, Ramon G de Oliveira, et al.Journal of Medicinal Chemistry|July 26, 2002
Synthesis, cytotoxicity, and antiplasmodial and antitrypanosomal activity of new neocryptolepine derivativesTim H M Jonckers, Sabine van Miert, Kanyanga Cimanga, et al.Plos Neglected Tropical Diseases|January 17, 2012
Integrated dataset of screening hits against multiple neglected disease pathogensSolomon Nwaka, Dominique Besson, Bernadette Ramirez, et al.Bioorganic & Medicinal Chemistry|August 6, 2019
Alkynamide phthalazinones as a new class of TbrPDEB1 inhibitors (Part 2)Erik de Heuvel, Abhimanyu K Singh, Pierre Boronat, et al.Jac-Antimicrobial Resistance|November 22, 2021
7-Aryl-7-deazapurine 3'-deoxyribonucleoside derivative as a novel lead for Chagas' disease therapy: in vitro and in vivo pharmacologyCamila Cardoso-Santos, Ludmila Ferreira de Almeida Fiuza, Cristiane França da Silva, et al.ACS Infectious Diseases|December 12, 2024
Discovery and Development of an Advanced Lead for the Treatment of African TrypanosomiasisKayhan Ilbeigi, Dorien Mabille, An Matheeussen, et al.The Journal of Antimicrobial Chemotherapy|March 31, 2026
A strategic discovery roadmap towards high-quality leads and drug development candidates for kinetoplastid diseases. Part 2: from molecule to confirmed hitSarah Hendrickx, Kayhan Ilbeigi, Eli S J Thoré, et al.The Journal of Antimicrobial Chemotherapy|May 5, 2026
A strategic discovery roadmap towards high-quality leads and drug development candidates for kinetoplastid diseases. Part 1: setting the stageSarah Hendrickx, Kayhan Ilbeigi, Eli S J Thoré, et al.Antimicrobial Agents and Chemotherapy|July 1, 2020
Efficacy of Novel Pyrazolone Phosphodiesterase Inhibitors in Experimental Mouse Models of Trypanosoma cruziJulianna Siciliano de Araújo, Cristiane França da Silva, Denise da Gama Jaén Batista, et al.Journal of Medicinal Chemistry|September 12, 2012
Catechol pyrazolinones as trypanocidals: fragment-based design, synthesis, and pharmacological evaluation of nanomolar inhibitors of trypanosomal phosphodiesterase B1Kristina M Orrling, Chimed Jansen, Xuan Lan Vu, et al.Pageof 27