| Literature DB >> 31257853 |
Theresa H Nguyen1, Nicole N Haese2, Nikhil Madadi1, Sanjay Sarkar3, Kiley Bonin2, Cassilyn E Streblow2, Sharon Taft-Benz3, Nichole A Tower4, Lynn Rasmussen4, Robert Bostwick4, Corinne E Augelli-Szafran1, Mark J Suto1, Thomas E Morrison5, Victor DeFilippis2, Mark T Heise3, Daniel N Streblow2, Ashish K Pathak1.
Abstract
Alphaviruses are arthropod-transmitted members of the Togaviridae family that can cause severe disease in humans, including debilitating arthralgia and severe neurological complications. Currently, there are no approved vaccines or antiviral therapies directed against the alphaviruses, and care is limited to treating disease symptoms. A phenotypic cell-based high-throughput screen was performed to identify small molecules that inhibit the replication of Venezuelan Equine Encephalitis Virus (VEEV). The compound, 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-N-(3-fluoro-4-methoxybenzyl)ethan-1-amine (1), was identified as a highly active, potent inhibitor of VEEV with an effective concentration for 90% inhibition of virus (EC90) of 0.89 μM and 7.49 log reduction in virus titers at 10 μM concentration. These data suggest that further investigation of compound 1 as an antiviral therapeutic against VEEV, and perhaps other alphaviruses, is warranted. Experiments suggested that the antiviral activity of compound 1 is directed at an early step in the VEEV replication cycle by blocking viral RNA and protein synthesis.Entities:
Keywords: VEEV; alphaviruses; antiviral inhibitors; dibenzyl amines
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Year: 2019 PMID: 31257853 DOI: 10.1021/acsinfecdis.9b00035
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084