Kaustav Khatua, Sandeep Atla, Demonta Coleman, Lauren R. Blankenship, Yugendar R. Alugubelli, Veerabhadra R. Vulupala, Xuejiao Shirley Guo, Hongjie Xia, Birte Kalveram, David H. Walker, Brett Hurst, Sathish Kumar, Chia-Chuan D. Cho, Shivangi Sharma, Kai Yang, Dorsa Rabie, Satyanarayana Nyalata, Benjamin W. Neuman, Xuping Xie, Shiqing Xu, Wenshe Ray Liu
Abstract Anecdotal reports about smoking that might prevent SARS-CoV-2 infection inspire the search for nicotine and its pyrolysis products as inhibitors of the SARS-CoV-2 main protease (M Pro ). This effort leads to the discovery of 3-vinylpyridine as an M Pro inhibitor. 3-Vinylpyridine resembles part of nirmatrelvir in binding to M Pro but does not involve a critical interaction with residue E166, whose mutation has led to resistance to nirmatrelvir. Integration of the two molecules, followed by a medicinal chemistry campaign, produces several molecules with better in vitro potency than nirmatrelvir. Two lead molecules, YR-C-136 and SR-B-103, display better pharmacokinetic characteristics than nirmatrelvir in virus-challenged male mice and much better antiviral efficacy in virus-challenged female mice. Both molecules maintain high potency in inhibiting the nirmatrelvir-resistant M Pro (E166V/L50F) variant. They also exhibit a broad and highly potent antiviral spectrum against most pathogenic coronaviruses. With high in vivo potency, both molecules are potentially standalone pan-antivirals for coronaviruses and may serve as countermeasures for future coronavirus outbreaks.