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J Med Chem . Discovery of Nirmatrelvir (PF-07321332): A Potent, Orally Active Inhibitor of the Severe Acute Respiratory Syndrome Coronavirus 2 (SAR

tetano

Editor, Senior Moderator
J Med Chem


. 2025 Feb 28.
doi: 10.1021/acs.jmedchem.4c02561. Online ahead of print. Discovery of Nirmatrelvir (PF-07321332): A Potent, Orally Active Inhibitor of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS CoV-2) Main Protease

Jamison B Tuttle[SUP] 1 [/SUP], Christophe Allais[SUP] 2 [/SUP], Charlotte M N Allerton[SUP] 1 [/SUP], Annaliesa S Anderson[SUP] 3 [/SUP], Joel T Arcari[SUP] 2 [/SUP], Lisa M Aschenbrenner[SUP] 2 [/SUP], Melissa Avery[SUP] 2 [/SUP], Justin Bellenger[SUP] 2 [/SUP], Simon Berritt[SUP] 2 [/SUP], Britton Boras[SUP] 4 [/SUP], Brian P Boscoe[SUP] 2 [/SUP], Leanne M Buzon[SUP] 2 [/SUP], Rhonda D Cardin[SUP] 3 [/SUP], Anthony A Carlo[SUP] 2 [/SUP], Karen J Coffman[SUP] 2 [/SUP], Alyssa Dantonio[SUP] 2 [/SUP], Li Di[SUP] 2 [/SUP], Heather Eng[SUP] 2 [/SUP], Kathleen A Farley[SUP] 2 [/SUP], Rose Ann Ferre[SUP] 4 [/SUP], Ketan S Gajiwala[SUP] 4 [/SUP], Scott A Gibson[SUP] 5 [/SUP], Samantha E Greasley[SUP] 4 [/SUP], Brett L Hurst[SUP] 5 [/SUP], Eugene P Kadar[SUP] 2 [/SUP], Amit S Kalgutkar[SUP] 1 [/SUP], Erik A Lachapelle[SUP] 2 [/SUP], Lorraine F Lanyon[SUP] 2 [/SUP], Jisun Lee[SUP] 2 [/SUP], Jack Lee[SUP] 2 [/SUP], Yajing Lian[SUP] 2 [/SUP], Wei Liu[SUP] 4 [/SUP], Luis A Martínez-Alsina[SUP] 2 [/SUP], Stephen W Mason[SUP] 3 [/SUP], Stephen Noell[SUP] 2 [/SUP], Jonathan Novak[SUP] 1 [/SUP], R Scott Obach[SUP] 2 [/SUP], Keving Ogilvie[SUP] 2 [/SUP], Steven V O'Neil[SUP] 2 [/SUP], Gregory Ostner[SUP] 2 [/SUP], Dafydd R Owen[SUP] 1 [/SUP], Nandini C Patel[SUP] 1 [/SUP], Martin Pettersson[SUP] 1 [/SUP], Ravi Shankar Singh[SUP] 1 [/SUP], Devendra K Rai[SUP] 2 [/SUP], Matthew R Reese[SUP] 2 [/SUP], Sylvie Sakata[SUP] 4 [/SUP], Matthew F Sammons[SUP] 1 [/SUP], Jean G Sathish[SUP] 3 [/SUP], Raman Sharma[SUP] 2 [/SUP], Claire M Steppan[SUP] 2 [/SUP], Al Stewart[SUP] 4 [/SUP], Lawrence Updyke[SUP] 2 [/SUP], Patrick R Verhoest[SUP] 1 [/SUP], Liuqing Wei[SUP] 2 [/SUP], Stephen W Wright[SUP] 2 [/SUP], Eddie Yang[SUP] 2 [/SUP], Qingyi Yang[SUP] 1 [/SUP], Yuao Zhu[SUP] 3 [/SUP]



Affiliations
Abstract

In early 2020, severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) infections leading to COVID-19 disease reached a global level leading to the World Health Organization (WHO) declaration of a pandemic. Scientists around the globe rapidly responded to try and discover novel therapeutics and repurpose extant drugs to treat the disease. This work describes the preclinical discovery efforts that led to the invention of PF-07321332 (nirmatrelvir, 14), a potent and orally active inhibitor of the SARS CoV-2 main protease (M[SUP]pro[/SUP]) enzyme. At the outset we focused on modifying PF-00835231 (1) discovered in 2004 as a potent inhibitor of the SARS CoV-1 M[SUP]pro[/SUP] with poor systemic exposure. Our effort was focused on modifying 1 with the goal of engineering in oral bioavailability by design, while maintaining cellular potency and low metabolic clearance. Modifications of 1 ultimately led to the invention of nirmatrelvir 14, the M[SUP]pro[/SUP] inhibitor component in PAXLOVID.


 
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