Discovery of GS-5245 (Obeldesivir), an Oral Prodrug of Nucleoside GS-441524 That Exhibits Antiviral Efficacy in SARS-CoV-2-Infected African Green Monkeys.
Richard L MackmanRao V KallaDarius BabusisJared PittsKimberly T BarrettKwon ChunVenice Du PontLauren RodriguezJasmine MoshiriYili XuMichael LeeGary LeeBlake BleierAnh-Quan NguyenB Michael O'KeefeAndrea AmbrosiMeredith CookJoy YuKassibla Elodie DempahElaine BunyanNicholas C RiolaXianghan LuRenmeng LiuAshley DavieTien-Ying HsiangJustin DearingMeghan VermillionMichael GaleAnita Niedziela-MajkaJoy Y FengCharlotte HedskogJohn P BilelloRaju SubramanianTomas CihlarPublished in: Journal of medicinal chemistry (2023)
Remdesivir 1 is an phosphoramidate prodrug that releases the monophosphate of nucleoside GS-441524 ( 2 ) into lung cells, thereby forming the bioactive triphosphate 2-NTP . 2-NTP , an analog of ATP, inhibits the SARS-CoV-2 RNA-dependent RNA polymerase replication and transcription of viral RNA. Strong clinical results for 1 have prompted interest in oral approaches to generate 2-NTP . Here, we describe the discovery of a 5'-isobutyryl ester prodrug of 2 (GS-5245, Obeldesivir, 3 ) that has low cellular cytotoxicity and 3-7-fold improved oral delivery of 2 in monkeys. Prodrug 3 is cleaved presystemically to provide high systemic exposures of 2 that overcome its less efficient metabolism to 2-NTP , leading to strong SARS-CoV-2 antiviral efficacy in an African green monkey infection model. Exposure-based SARS-CoV-2 efficacy relationships resulted in an estimated clinical dose of 350-400 mg twice daily. Importantly, all SARS-CoV-2 variants remain susceptible to 2 , which supports development of 3 as a promising COVID-19 treatment.