Matthew N. O'Brien Laramy

Dr. Matthew N. O'Brien Laramy

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Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 February 2019 in Nature Reviews Materials
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Journal Article
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CLChristine R. Laramy
Christine R. Laramy
MLMatthew N. O'Brien Laramy
Matthew N. O'Brien Laramy
CMChad Mirkin
Chad Mirkin

2 May 2013 in Angewandte Chemie International Edition
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Journal Article
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RMRobert J. Macfarlane
Robert J. Macfarlane
MLMatthew N. O'Brien Laramy
Matthew N. O'Brien Laramy
SPSarah Hurst Petrosko
Sarah Hurst Petrosko
CMChad Mirkin
Chad Mirkin

1 August 2021 in Journal of Controlled Release
Verified
Journal Article
Closed access
MLMatthew N. O'Brien Laramy
Matthew N. O'Brien Laramy
WJWenlei Jiang
Wenlei Jiang
YWYan Wang
Yan Wang
DLDavid M. Loffredo
David M. Loffredo

21 February 2023 in Nature Reviews Drug Discovery
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Journal Article
Closed access
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MLMatthew N. O'Brien Laramy
Matthew N. O'Brien Laramy
SLSuman Luthra
Suman Luthra
MBMatthew F. Brown
Matthew F. Brown
DBDerek W. Bartlett
Derek W. Bartlett

18 July 2023 in Molecular Pharmaceutics
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Journal Article
Closed access
MLMatthew N. O'Brien Laramy
Matthew N. O'Brien Laramy
ACAntonio P. Costa
Antonio P. Costa
YCYareli Maciel Cebrero
Yareli Maciel Cebrero
JJJohnson Joseph
Johnson Joseph
ASApoorva Sarode
Apoorva Sarode
GHGreg L. Hura
Greg L. Hura

13 September 2020 in bioRxiv
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Preprint
Open access
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BBBritton Boras
Britton Boras
RJRhys M Jones
Rhys M Jones
BABrandon J Anson
Brandon J Anson
DADan Arenson
Dan Arenson
LALisa Aschenbrenner
Lisa Aschenbrenner
CACharlotte Allerton
Charlotte Allerton
COVID-19 caused by the SARS-CoV-2 virus has become a global pandemic. 3CL protease is a virally encoded protein that is essential across a broad spectrum of coronaviruses with no close human analogs. The designed phosphate prodrug PF-07304814 is metabolized to PF-00835321 which is a potent inhibitor in vitro of the coronavirus family 3CL pro, with selectivity over human host protease targets. Furthermore, PF-00835231 exhibits potent in vitro antiviral activity against SARS-CoV-2 as a single agent and it is additive/synergistic in combination with remdesivir. We present the ADME, safety, in vitro , and in vivo antiviral activity data that supports the clinical evaluation of this compound as a potential COVID-19 treatment.