ACS infectious diseases · 2019
Studies on Dibenzylamines as Inhibitors of Venezuelan Equine Encephalitis Virus.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Nguyen Theresa H, Haese Nicole N, Madadi Nikhil, Sarkar Sanjay, Bonin Kiley, Streblow Cassilyn E, Taft-Benz Sharon, Tower Nichole A, Rasmussen Lynn, Bostwick Robert, Augelli-Szafran Corinne E, Suto Mark J, Morrison Thomas E, DeFilippis Victor, Heise Mark T, Streblow Daniel N, Pathak Ashish K
Аннотация
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.