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Showing 1–7 of 7 results
Advanced filters: Author: Laste Stojanovski Clear advanced filters
  • Tuberculosis is a major cause of mortality, and the rise of drug-resistant strains of Mycobacterium tuberculosis requires the urgent development of safe and effective treatments. In this work, the authors develop a compound against lysyl-tRNA synthetase, demonstrating on-target mechanism of action and efficacy in vivo.

    • Simon R. Green
    • Susan H. Davis
    • Laura A. T. Cleghorn
    ResearchOpen Access
    Nature Communications
    Volume: 13, P: 1-12
  • An automated approach designing drug ligands to multi-target profiles (with a 75% prediction success rate) is experimentally validated by the invention of novel ligands tailored to the complex and physiologically-relevant goal of identifying drugs that can specifically target profiles of multiple proteins.

    • Jérémy Besnard
    • Gian Filippo Ruda
    • Andrew L. Hopkins
    Research
    Nature
    Volume: 492, P: 215-220
  • The description of a compound (DDD107498) with antimalarial activity against multiple life-cycle stages of Plasmodium falciparum and good pharmacokinetic and safety properties, with potential for single-dose treatment, chemoprotection and prevention of transmission.

    • Beatriz Baragaña
    • Irene Hallyburton
    • Ian H. Gilbert
    Research
    Nature
    Volume: 522, P: 315-320
  • African sleeping sickness, caused by Trypanosoma brucei species, is responsible for some 30,000 human deaths each year. Available treatments are limited by poor efficacy and safety profiles. However, a new molecular target for potential treatments has now been identified. The protein target is T. brucei N-myristoyltransferase. In further experiments, lead compounds have been discovered that inhibit this protein, kill trypanosomes in vitro and in vivo, and can cure trypanosomiasis in mice.

    • Julie A. Frearson
    • Stephen Brand
    • Paul G. Wyatt
    Research
    Nature
    Volume: 464, P: 728-732