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- M Javad Aman, Michael S Kinch, Kelly Warfield, Travis Warren, Abdul Yunus, Sven Enterlein, Eric Stavale, Peifang Wang, Shaojing Chang, Qingsong Tang, Kevin Porter, Michael Goldblatt, and Sina Bavari.
- United States Army Medical Research Institute for Infectious Diseases, Fort Detrick, MD 21702, USA. mkinch@functional-genetics.com
- Antiviral Res. 2009 Sep 1; 83 (3): 245-51.
AbstractWe report herein the identification of a small molecule therapeutic, FGI-106, which displays potent and broad-spectrum inhibition of lethal viral hemorrhagic fevers pathogens, including Ebola, Rift Valley and Dengue Fever viruses, in cell-based assays. Using mouse models of Ebola virus, we further demonstrate that FGI-106 can protect animals from an otherwise lethal infection when used either in a prophylactic or therapeutic setting. A single treatment, administered 1 day after infection, is sufficient to protect animals from lethal Ebola virus challenge. Cell-based assays also identified inhibitory activity against divergent virus families, which supports a hypothesis that FGI-106 interferes with a common pathway utilized by different viruses. These findings suggest FGI-106 may provide an opportunity for targeting viral diseases.
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