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Updated: Mar 22, 2026

Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
Novel diversity-oriented synthesis-derived respiratory syncytial virus inhibitors identified via a high throughput
Jeremy R Duvall1, Lynn VerPlank1, Barbara Ludeke2
1Broad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142, United States.
Abstract:
Respiratory syncytial virus (RSV) infections affect millions of children and adults every year. Despite the significant disease burden, there are currently no safe and effective vaccines or therapeutics. We employed a replicon-based high throughput screen combined with live-virus triaging assays to identify three novel diversity-oriented synthesis-derived scaffolds with activity against RSV. One of these small molecules is shown to target the RSV polymerase (L protein) to inhibit viral replication and transcription; the mechanisms of action of the other small molecules are currently unknown. The compounds described herein may provide attractive inhibitors for lead optimization campaigns.

