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Discovery of JNJ-1802, a First-in-Class Pan-Serotype Dengue Virus NS4B Inhibitor.

Bart KesteleynJean-François BonfantiDorothée BardiotBenoît De BoeckOlivia GoethalsSuzanne J F KapteinBart StoopsErwin CoesemansJérôme FortinPhilippe MullerFrédéric DoubletGunter CarlensMohamed KoukniWim SmetsPierre RaboissonPatrick ChaltinKenny SimmenMarnix Van LoockJohan NeytsArnaud MarchandTim H M Jonckers
Published in: Journal of medicinal chemistry (2024)
Dengue is a global public health threat, with about half of the world's population at risk of contracting this mosquito-borne viral disease. Climate change, urbanization, and global travel accelerate the spread of dengue virus (DENV) to new areas, including southern parts of Europe and the US. Currently, no dengue-specific small-molecule antiviral for prophylaxis or treatment is available. Here, we report the discovery of JNJ-1802 as a potent, pan-serotype DENV inhibitor (EC 50 's ranging from 0.057 to 11 nM against the four DENV serotypes). The observed oral bioavailability of JNJ-1802 across preclinical species, its low clearance in human hepatocytes, the absence of major in vitro pharmacology safety alerts, and a dose-proportional increase in efficacy against DENV-2 infection in mice were all supportive of its selection as a development candidate against dengue. JNJ-1802 is being progressed in clinical studies for the prevention or treatment of dengue.
Keyphrases
  • dengue virus
  • zika virus
  • aedes aegypti
  • small molecule
  • public health
  • climate change
  • endothelial cells
  • high throughput
  • sars cov
  • stem cells
  • mesenchymal stem cells
  • skeletal muscle
  • anti inflammatory
  • replacement therapy