Researchers discover highly potent compound that blocks Ebola virus entry
New compound is more than 100 times more potent than previously reported Ebola entry inhibitors and shows strong protection following oral treatment in a preclinical model
MINNEAPOLIS/ST. PAUL (9/9/2026) — A University of Minnesota-led multi-institutional research team has discovered a highly potent small molecule that blocks Ebola virus entry by stabilizing the virus's entry protein and provides strong protection when given orally in a preclinical model.
The study, recently published in Nature CommunicationsExternal link that opens in the same window, resulted from extensive collaboration among the University of Minnesota, Baylor College of Medicine, Boston University and the University of Florida Scripps Institute, with support from the NIH-funded Midwest Antiviral Drug Discovery (AViDD) Center, based at the University of Minnesota.
MWAC-3634 targets the Ebola virus entry protein. All previously structurally characterized small molecules targeting this protein destabilized it. MWAC-3634 instead stabilizes the entry protein, preventing the shape changes required for viral entry. It is also at least 100 times more potent than previously reported small-molecule Ebola entry inhibitors.
“This compound works in the opposite way from previously studied Ebola entry inhibitors,” said Fang Li, PhD, professor of pharmacology at the University of Minnesota Medical School and co-director of the Midwest AViDD Center. “Earlier compounds destabilized the Ebola entry protein. MWAC-3634 stabilizes it, essentially locking the protein so the virus cannot make the changes required to enter a cell. That reveals a new strategy for blocking infection.”
From billions of molecules to a lead compound
Researchers used DNA-Encoded Chemistry Technology to screen approximately 4.73 billion molecules directly against the Ebola entry protein, uncovering a promising chemical starting point.
“DNA-encoded libraries let us search billions of molecules in a single discovery campaign,” said Srinivas Chamakuri, PhD, assistant director of the Center for Drug Discovery in the Department of Pathology at Baylor College of Medicine. “That scale allowed us to explore chemical space far beyond a conventional screen and uncover a promising starting point we might otherwise have missed.”
Stereochemical analysis of the initial hit identified MWAC-3634 as the most active form. Against authentic Ebola virus, the compound inhibited infection with an IC50 of 0.65 nM and showed no detectable toxicity to cells under the conditions tested.
“The initial hit was only a starting point,” said Peter Dosa, PhD, research associate professor of medicinal chemistry at the University of Minnesota. “The starting compound was a mixture of closely related forms. By identifying the most active form, we substantially increased its potency.”
How the compound locks the entry protein
High-resolution structural studies showed that MWAC-3634 fits into a pocket in the Ebola entry protein and holds it in a stable state. Normally, the protein must change shape for the virus to fuse with and enter a host cell. Locking it in place blocks infection at one of its earliest stages.
“The structure allowed us to see exactly where MWAC-3634 binds and how it stabilizes the Ebola entry protein,” said Dr. Li. “That molecular view helps explain the compound’s high potency and gives us a blueprint for designing improved versions.”
In a preclinical model, oral treatment with MWAC-3634 substantially improved survival, reduced signs of illness and lowered virus levels. The compound also showed 69% oral bioavailability relative to intravenous dosing.
“The protection we saw with oral treatment is particularly encouraging,” said Robert Davey, PhD, professor of virology, immunology and microbiology and interim director of the National Emerging Infectious Diseases Laboratories at Boston University. “This is still an early-stage compound, and additional development and testing will be needed before we know whether it could be useful in people.”
Fan Bu is the lead author of the study; Bu, Gang Ye, Kiran L. Sharma and Bruno La Rosa contributed equally to the work. Li is the senior author; Li, Peter Dosa, Srinivas Chamakuri and Robert Davey are co-corresponding authors.
The study combined DNA-encoded library screening, stereochemical analysis, structural biology, authentic Ebola virus testing, drug exposure studies and animal studies across four institutions. It was supported by the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health, including the Midwest AViDD Center (U19AI171954), and by NIH grant R01AI195592. MWAC-3634 is experimental and has not been approved or shown to prevent or treat Ebola virus disease in humans.
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About the University of Minnesota Medical School
The University of Minnesota Medical School is at the forefront of learning and discovery, transforming medical care and educating the next generation of physicians. Our graduates and faculty produce high-impact biomedical research and advance the practice of medicine. We acknowledge that the U of M Medical School is located on traditional, ancestral and contemporary lands of the Dakota and the Ojibwe, and scores of other Indigenous people, and we affirm our commitment to tribal communities and their sovereignty as we seek to improve and strengthen our relations with tribal nations. Learn more at med.umn.edu.
Journal
Nature Communications
Method of Research
Experimental study
Subject of Research
Animals
Article Title
A small molecule inhibits Ebola virus entry through glycoprotein stabilization
Article Publication Date
1-Sep-2026
COI Statement
The University of Minnesota has filed patents on MWAC-2600, 2601, 2807, 2808, 3006, 3634, and 4219 with F.L., P.D., F.B., G.Y., M.M.M., D.W.Y., S.C., and M.P. as inventors. The remaining authors declare no competing interests.
