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Plos Neglected Tropical Diseases|October 23, 2013
Exploring the Trypanosoma brucei Hsp83 potential as a target for structure guided drug designJuan Carlos Pizarro, Tanya Hills, Guillermo Senisterra, et al.Chemmedchem|November 20, 2009
Investigation of trypanothione reductase as a drug target in Trypanosoma bruceiDaniel Spinks, Emma J Shanks, Laura A T Cleghorn, et al.The Journal of Biological Chemistry|October 16, 2009
Chemical validation of trypanothione synthetase: a potential drug target for human trypanosomiasisLeah S Torrie, Susan Wyllie, Daniel Spinks, et al.Bioorganic & Medicinal Chemistry Letters|August 15, 2018
2,4-Diamino-6-methylpyrimidines for the potential treatment of Chagas' diseaseMichael G Thomas, Manu De Rycker, Ignacio Cotillo Torrejon, et al.Antimicrobial Agents and Chemotherapy|May 31, 2018
Antitrypanosomal 8-Hydroxy-Naphthyridines Are Chelators of Divalent Transition MetalsRichard J Wall, Sonia Moniz, Michael G Thomas, et al.Chemmedchem|June 19, 2013
From on-target to off-target activity: identification and optimisation of Trypanosoma brucei GSK3 inhibitors and their characterisation as anti-Trypanosoma brucei drug discovery lead moleculesAndrew Woodland, Raffaella Grimaldi, Torsten Luksch, et al.Tetrahedron Letters|May 7, 2019
Optimisation of a key cross-coupling reaction towards the synthesis of a promising antileishmanial compoundRaul F Velasco, César Guerrero, Gloria Fra, et al.Plos Computational Biology|December 17, 2013
Handling uncertainty in dynamic models: the pentose phosphate pathway in Trypanosoma bruceiEduard J Kerkhoven, Fiona Achcar, Vincent P Alibu, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|July 9, 2008
Kinetic properties and inhibition of the dimeric dUTPase-dUDPase from Campylobacter jejuniJuan A Musso-Buendía, Antonio E Vidal, Ganasan Kasinthan, et al.Journal of Medicinal Chemistry|September 29, 2006
Evaluation of azasterols as anti-parasiticsLudovic Gros, Silvia Orenes Lorente, Carmen Jimenez Jimenez, et al.Pageof 19