TY - JOUR
T1 - A strategic discovery roadmap towards high-quality leads and drug development candidates for kinetoplastid diseases. Part 2: from molecule to confirmed hit
AU - Hendrickx, Sarah
AU - Ilbeigi, Kayhan
AU - Thore, Eli S. J.
AU - Bertram, Michael G.
AU - Calvo-Alvarez, Estefania
AU - Cintesun, Sener
AU - Olias-Molero, Ana Isabel
AU - Corral, Maria Jesus
AU - Mateo-Barrientos, Marta
AU - Estaquier, Jerome
AU - Pomel, Sebastien
AU - Alunda, Jose Maria
AU - Gul, Sheraz
AU - Van Bocxlaer, Katrien
AU - Frezard, Frederic
AU - Tavares, Joana
AU - Cordeiro Da Silva, Anabela
AU - Costi, Maria Paola
AU - Maes, Louis
AU - Caljon, Guy
PY - 2026
Y1 - 2026
N2 - Given the medical importance and challenges related to kinetoplastid diseases, a strategic roadmap is needed for the identification of high-quality leads and drug development candidates. Within the aim to deliver more compelling proof-of-concept read-outs, this part proposes a systematic flow-chart of laboratory experiments and decision criteria, focusing on African trypanosomiasis, Chagas disease and visceral and cutaneous leishmaniasis. Next to precision experimental design and reporting, an overview is provided of various complementary laboratory models reproducing kinetoplastid infection and disease. Technical aspects of conventional in vitro and in vivo approaches and, more recently, in silico methods are presented with reference to specific preclinical R&D stages from 'hit finding' to 'profiling of a confirmed hit', covering the expertise areas of medicinal chemistry, primary pharmacology, (eco)toxicology, pharmacokinetics and pharmaceutics (Figure 1).
AB - Given the medical importance and challenges related to kinetoplastid diseases, a strategic roadmap is needed for the identification of high-quality leads and drug development candidates. Within the aim to deliver more compelling proof-of-concept read-outs, this part proposes a systematic flow-chart of laboratory experiments and decision criteria, focusing on African trypanosomiasis, Chagas disease and visceral and cutaneous leishmaniasis. Next to precision experimental design and reporting, an overview is provided of various complementary laboratory models reproducing kinetoplastid infection and disease. Technical aspects of conventional in vitro and in vivo approaches and, more recently, in silico methods are presented with reference to specific preclinical R&D stages from 'hit finding' to 'profiling of a confirmed hit', covering the expertise areas of medicinal chemistry, primary pharmacology, (eco)toxicology, pharmacokinetics and pharmaceutics (Figure 1).
UR - https://res.slu.se/id/publ/146665
U2 - 10.1093/jac/dkag110
DO - 10.1093/jac/dkag110
M3 - Review article
C2 - 41913953
SN - 0305-7453
VL - 81
JO - Journal of Antimicrobial Chemotherapy
JF - Journal of Antimicrobial Chemotherapy
IS - 4
M1 - dkag110
ER -