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Biorxiv : the Preprint Server for Biology|January 18, 2024
Discovery of 2-amide-3-methylester thiophenes that target SARS-CoV-2 Mac1 and repress coronavirus replication, validating Mac1 as an anti-viral targetSarah Wazir, Tomi A O Parviainen, Jessica J Pfannenstiel, et al.
Journal of Medicinal Chemistry|April 9, 2024
Discovery of 2-Amide-3-methylester Thiophenes that Target SARS-CoV-2 Mac1 and Repress Coronavirus Replication, Validating Mac1 as an Antiviral TargetSarah Wazir, Tomi A O Parviainen, Jessica J Pfannenstiel, et al.
Journal of Virology|November 7, 2020
The SARS-CoV-2 Conserved Macrodomain Is a Mono-ADP-RibosylhydrolaseYousef M O Alhammad, Maithri M Kashipathy, Anuradha Roy, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2023
SARS-CoV-2 Mac1 is required for IFN antagonism and efficient virus replication in miceYousef M Alhammad, Srivatsan Parthasarathy, Roshan Ghimire, et al.
Biorxiv : the Preprint Server for Biology|June 9, 2020
The SARS-CoV-2 conserved macrodomain is a mono-ADP-ribosylhydrolaseYousef M O Alhammad, Maithri M Kashipathy, Anuradha Roy, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2023
SARS-CoV-2 nsp15 endoribonuclease antagonizes dsRNA-induced antiviral signalingClayton J Otter, Nicole Bracci, Nicholas A Parenti, et al.
RSC Chemical Biology|June 29, 2026
Cellular engagement of the SARS-CoV-2 macrodomain by GS-441524 and enhanced <i>in vitro</i> inhibition by its diphosphorylated metaboliteBanhi Biswas, Junlin Zhuo, Jürgen Bosch, et al.
Biorxiv : the Preprint Server for Biology|March 9, 2022
Design, Synthesis and Evaluation of Inhibitors of the SARS-CoV2 nsp3 MacrodomainLavinia M Sherrill, Elva E Joya, AnnMarie Walker, et al.
Bioorganic & Medicinal Chemistry|May 21, 2022
Design, synthesis and evaluation of inhibitors of the SARS-CoV-2 nsp3 macrodomainLavinia M Sherrill, Elva E Joya, AnnMarie Walker, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
Mutation of a highly conserved isoleucine residue in loop 2 of several <i>β</i>-coronavirus macrodomains indicates that enhanced ADP-ribose binding is detrimental to infectionCatherine M Kerr, Jessica J Pfannenstiel, Yousef M Alhammad, et al.
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