
This review explores small-molecule antivirals as chemical probes to stabilize fleeting polymerase conformations in pneumo- and paramyxoviruses. By assessing distinct classes of polymerase inhibitors with established structure-activity relationships and resistance profiles, it highlights their roles in blocking essential polymerase domain rearrangements. These probes not only provide insights into viral polymerase structures but also underscore promising druggable targets for antiviral development.
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