Identification and Profiling of a Novel Diazaspiro[3.4]octane Chemical Series Active against Multiple Stages of the Human Malaria Parasite Plasmodium falciparum and Optimization Efforts

A novel diazaspiro[3.4]­octane series was identified from a Plasmodium falciparum whole-cell high-throughput screening campaign. Hits displayed activity against multiple stages of the parasite lifecycle, which together with a novel sp3-rich scaffold provided an attractive starting point for a hit-to...

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Veröffentlicht in:Journal of medicinal chemistry 2021-02, Vol.64 (4), p.2291-2309
Hauptverfasser: Le Manach, Claire, Dam, Jean, Woodland, John G, Kaur, Gurminder, Khonde, Lutete P, Brunschwig, Christel, Njoroge, Mathew, Wicht, Kathryn J, Horatscheck, André, Paquet, Tanya, Boyle, Grant A, Gibhard, Liezl, Taylor, Dale, Lawrence, Nina, Yeo, Tomas, Mok, Sachel, Eastman, Richard T, Dorjsuren, Dorjbal, Talley, Daniel C, Guo, Hui, Simeonov, Anton, Reader, Janette, van der Watt, Mariëtte, Erlank, Erica, Venter, Nelius, Zawada, Jacek W, Aswat, Ayesha, Nardini, Luisa, Coetzer, Theresa L, Lauterbach, Sonja B, Bezuidenhout, Belinda C, Theron, Anjo, Mancama, Dalu, Koekemoer, Lizette L, Birkholtz, Lyn-Marie, Wittlin, Sergio, Delves, Michael, Ottilie, Sabine, Winzeler, Elizabeth A, von Geldern, Thomas W, Smith, Dennis, Fidock, David A, Street, Leslie J, Basarab, Gregory S, Duffy, James, Chibale, Kelly
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Sprache:eng
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Zusammenfassung:A novel diazaspiro[3.4]­octane series was identified from a Plasmodium falciparum whole-cell high-throughput screening campaign. Hits displayed activity against multiple stages of the parasite lifecycle, which together with a novel sp3-rich scaffold provided an attractive starting point for a hit-to-lead medicinal chemistry optimization and biological profiling program. Structure–activity-relationship studies led to the identification of compounds that showed low nanomolar asexual blood-stage activity (
ISSN:0022-2623
1520-4804
DOI:10.1021/acs.jmedchem.1c00034