Why the study?
RdRp is an essential enzyme for viral replication and an optimal target for antiviral drug development, but the lack of structural details on catalytically-competent or ligand-bound RdRp can hamper structure-based drug design.
Design
Review
Key result
Structure-based drug design targeting the RNA-dependent RNA polymerase has yielded successful antivirals for HCV and SARS-CoV-2, but progress in Flaviviruses is hampered by a lack of structural data.
Authors
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RdRp targeting may guide antivirals in virus-related cardiac injury; leaves open specific cardiovascular applications.
Structure-based drug design targeting RdRp has been successful for HCV and SARS-CoV-2, but is hindered in Flaviviruses due to a lack of detailed structural information.
Picarazzi et al. (2020) conducted a review in Emerging RNA viruses (Coronaviruses, Flaviviruses, HCV). Structure-based drug design targeting RdRp was evaluated. Structure-based drug design targeting the RNA-dependent RNA polymerase has yielded successful antivirals for HCV and SARS-CoV-2, but progress in Flaviviruses is hampered by a lack of structural data.
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