2. Academic Validation
  3. Optimization of Species-Selective Reversible Proteasome Inhibitors for the Treatment of Malaria

Optimization of Species-Selective Reversible Proteasome Inhibitors for the Treatment of Malaria

  • J Med Chem. 2025 Nov 13;68(21):23485-23520. doi: 10.1021/acs.jmedchem.5c02394.
Suraksha Gahalawat 1,  Sneha Ray 1,  Xiaoyu Zhang 1,  Xiaoyi Deng 1,  Yan Han 2,  Zhe Chen 2,  Aloysus Lawong 1,  David M Shackleford 3,  Kasiram Katneni 3,  Gong Chen 3,  Peng Li 3,  Alice Ng 3,  Longjin Zhong 3,  Meiyu Hu 3,  Mitchell McInerney 3,  Wen Wang 3,  Jessica Saunders 3,  Daniel Collins 3,  Jaya Jayaseelan 3,  Cassandra L Noack 3,  Bikash C Maity 4,  Nirupam De 4,  Benoît Laleu 5,  Simon F Campbell 5,  Margaret A Phillips 1,  Susan A Charman 3,  Joseph M Ready 1
Affiliations

Affiliations

  • 1 Department of Biochemistry, UT Southwestern Medical Center, Dallas, Texas 75390, United States.
  • 2 Department of Biophysics, UT Southwestern Medical Center, Dallas, Texas 75390, United States.
  • 3 Centre for Drug Candidate Optimisation, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria 3052, Australia.
  • 4 TCG Lifesciences Pvt. Ltd., Kolkata 700091, West Bengal, India.
  • 5 MMV Medicines for Malaria Venture, ICC, Route de Pré-Bois 20, 1215 Geneva, Switzerland.
PMID: 41148577 DOI: 10.1021/acs.jmedchem.5c02394
Abstract

Malaria remains a critical global health challenge, with increasing resistance to frontline therapies necessitating novel drug targets. The Proteasome has emerged as a promising target for antimalarial drug discovery. This study describes efforts to optimize a series of species-selective reversible inhibitors targeting the Plasmodium falciparum 20S Proteasome. Starting from the carboxypiperidine scaffold identified through a high-throughput viability screen, we conducted iterative structure-activity relationship studies, leading to the development of highly potent and selective inhibitors with good oral bioavailability. Lead compounds demonstrated nanomolar potency against P. falciparum blood-stage parasites and selective inhibition of the parasite Proteasome over the human counterpart. Cryo-EM structural studies confirmed binding at the β5 subunit, while in vivo pharmacokinetic studies identified promising candidates for further development. These findings support Proteasome inhibition as a viable strategy for novel antimalarial drug development.

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