Remdesivir was widely used for hospitalised COVID-19 patients requiring supplemental oxygen. Its mechanism of action is best described as:
- A Inhibition of the viral main protease required for polyprotein cleavage
- B Induction of lethal mutagenesis during viral genome copying
- C Blockade of host ACE2 receptors preventing viral entry
- D Delayed chain termination after incorporation by viral RNA-dependent RNA polymerase ✓
Explanation
Remdesivir is a nucleoside analogue prodrug converted to its active triphosphate, which is incorporated by the SARS-CoV-2 RNA-dependent RNA polymerase. It terminates replication after a few additional nucleotides are added, a delayed chain termination that partially evades proofreading by exoribonuclease. Nirmatrelvir inhibits the main protease instead, monoclonal antibodies block spike-ACE2 binding, and molnupiravir acts by inducing mutagenesis of viral genomes.
Reference: Katzung's Basic and Clinical Pharmacology, 16th ed.
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Written and medically reviewed by the StethoPrep medical team.