Drug intelligence / Profile preview

deuteriumremidvir

Development stage
Phase 1
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Oral
01

Overview

Deuteriumremidvir refers to a deuterated analogue of remdesivir, an antiviral drug originally developed for the treatment of COVID-19. Deuteration involves replacing certain hydrogen atoms in the molecule with deuterium, a stable isotope of hydrogen. This modification can improve metabolic stability and pharmacokinetic properties without significantly altering the drug’s mechanism of action. Like remdesivir, deuteriumremidvir is expected to act as a nucleoside analog prodrug that inhibits viral RNA-dependent RNA polymerase (RdRp), thereby blocking viral replication. The parent compound, remdesivir, is approved for use against SARS-CoV-2 infection and works by causing delayed chain termination during viral RNA synthesis[6][8]. Deuterated analogues have been synthesized and shown to retain similar antiviral activity in vitro against SARS-CoV-2[4][3]. These modifications are under investigation for potential improvements in oral bioavailability and therapeutic profile.

Other names
deuterated remdesivir
02

Targets

RdRp (Coronavirus RNA-dependent RNA polymerase)

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