posted on 2024-06-11, 23:44authored bySovitj Pou, Rolf W. Winter, Rozalia A. Dodean, Katherine Liebman, Yuexin Li, Michael W. Mather, Binod Nepal, Aaron Nilsen, Mason J. Handford, Teresa M. Riscoe, Sydney Laxson, Payton J. Kirtley, Maya Aleshnick, Lev N. Zakharov, Jane X. Kelly, Martin J. Smilkstein, Brandon K. Wilder, Sandhya Kortagere, Akhil B. Vaidya, P. Holland Alday, J. Stone Doggett, Michael K. Riscoe
ELQ-300 is a potent antimalarial drug with activity against
blood,
liver, and vector stages of the disease. A prodrug, ELQ-331, exhibits reduced crystallinity and improved in vivo efficacy in
preclinical testing, and currently, it is in the developmental pipeline
for once-a-week dosing for oral prophylaxis against malaria. Because
of the high cost of developing a new drug for human use and the high
risk of drug failure, it is prudent to have a back-up plan in place.
Here we describe ELQ-596, a member of a new subseries
of 3-biaryl-ELQs, with enhanced potency in vitro against multidrug-resistant Plasmodium falciparum parasites. ELQ-598, a prodrug of ELQ-596 with diminished crystallinity,
is more effective vs murine malaria than its progenitor ELQ-331 by 4- to 10-fold, suggesting that correspondingly lower doses could
be used to protect and cure humans of malaria. With a longer bloodstream
half-life in mice compared to its progenitor, ELQ-596 highlights a novel series of next-generation ELQs with the potential
for once-monthly dosing for protection against malaria infection.
Advances in the preparation of 3-biaryl-ELQs are presented along with
preliminary results from experiments to explore key structure–activity
relationships for drug potency, selectivity, pharmacokinetics, and
safety.