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Discovery of Membrane-Bound Pyrophosphatase Inhibitors Derived from an Isoxazole Fragment

[Image: see text] Membrane-bound pyrophosphatases (mPPases) regulate energy homeostasis in pathogenic protozoan parasites and lack human homologues, which makes them promising targets in e.g. malaria. Yet only few nonphosphorus inhibitors have been reported so far. Here, we explore an isoxazole frag...

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Detalles Bibliográficos
Autores principales: Johansson, Niklas G., Turku, Ainoleena, Vidilaseris, Keni, Dreano, Loïc, Khattab, Ayman, Ayuso Pérez, Daniel, Wilkinson, Aaron, Zhang, Yuezhou, Tamminen, Matti, Grazhdankin, Evgeni, Kiriazis, Alexandros, Fishwick, Colin W. G., Meri, Seppo, Yli-Kauhaluoma, Jari, Goldman, Adrian, Boije af Gennäs, Gustav, Xhaard, Henri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153278/
https://www.ncbi.nlm.nih.gov/pubmed/32292570
http://dx.doi.org/10.1021/acsmedchemlett.9b00537
Descripción
Sumario:[Image: see text] Membrane-bound pyrophosphatases (mPPases) regulate energy homeostasis in pathogenic protozoan parasites and lack human homologues, which makes them promising targets in e.g. malaria. Yet only few nonphosphorus inhibitors have been reported so far. Here, we explore an isoxazole fragment hit, leading to the discovery of small mPPase inhibitors with 6–10 μM IC(50) values in the Thermotoga maritima test system. Promisingly, the compounds retained activity against Plasmodium falciparum mPPase in membranes and inhibited parasite growth.