Recent advances in the discovery of potent proteases inhibitors targeting the SARS coronaviruses

A Sharma, K Kaliya, SK Maurya - Current Topics in Medicinal …, 2021 - ingentaconnect.com
Across the globe, countries are being challenged by the SARS-CoV-2 (COVID-19)
pandemic in ways they have never been before. The global outbreak of SARS-CoV-2 with …

Characterization and inhibition of SARS-coronavirus main protease

PH Liang - Current topics in medicinal chemistry, 2006 - ingentaconnect.com
Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a
novel human coronavirus (CoV). During the 2003 epidemic, the disease rapidly spread from …

Synthesis, docking studies, and evaluation of pyrimidines as inhibitors of SARS-CoV 3CL protease

R Ramajayam, KP Tan, HG Liu, PH Liang - Bioorganic & medicinal …, 2010 - Elsevier
A series of 2-(benzylthio)-6-oxo-4-phenyl-1, 6-dihydropyrimidine as SARS-CoV 3CL
protease inhibitors were developed and their potency was evaluated by in vitro protease …

Structure‐activity relationships of benzamides and isoindolines designed as SARS‐CoV protease inhibitors effective against SARS‐CoV‐2

A Welker, C Kersten, C Müller, R Madhugiri… - …, 2021 - Wiley Online Library
Inhibition of coronavirus (CoV)‐encoded papain‐like cysteine proteases (PLpro) represents
an attractive strategy to treat infections by these important human pathogens. Herein we …

A Critical Study on Acylating and Covalent Reversible Fragment Inhibitors of SARS‐CoV‐2 Main Protease Targeting the S1 Site with Pyridine

R Wamser, S Pach, C Arkona, M Baumgardt… - …, 2023 - Wiley Online Library
SARS coronavirus main proteases (3CL proteases) have been validated as
pharmacological targets for the treatment of coronavirus infections. Current inhibitors of …

Structure and function of SARS-CoV and SARS-CoV-2 main proteases and their inhibition: A comprehensive review

X Li, Y Song - European Journal of Medicinal Chemistry, 2023 - Elsevier
Severe acute respiratory syndrome-associated coronavirus (SARS-CoV) identified in 2003
infected∼ 8000 people in 26 countries with 800 deaths, which was soon contained and …

[HTML][HTML] Targeting severe acute respiratory syndrome-coronavirus (SARS-CoV-1) with structurally diverse inhibitors: a comprehensive review

MS Hosseini-Zare, R Thilagavathi, C Selvam - RSC advances, 2020 - pubs.rsc.org
Coronaviruses, which were discovered in 1968, can lead to some human viral disorders, like
severe acute respiratory syndrome (SARS), Middle East respiratory syndrome-related …

Chalcones isolated from Angelica keiskei inhibit cysteine proteases of SARS-CoV

JY Park, JA Ko, DW Kim, YM Kim, HJ Kwon… - Journal of enzyme …, 2016 - Taylor & Francis
Two viral proteases of severe acute respiratory syndrome coronavirus (SARS-CoV), a
chymotrypsin-like protease (3CLpro) and a papain-like protease (PLpro) are attractive …

Synthesis, modification and docking studies of 5-sulfonyl isatin derivatives as SARS-CoV 3C-like protease inhibitors

W Liu, HM Zhu, GJ Niu, EZ Shi, J Chen, B Sun… - Bioorganic & medicinal …, 2014 - Elsevier
Abstract The Severe Acute Respiratory Syndrome (SARS) is a serious life-threatening and
strikingly mortal respiratory illness caused by SARS-CoV. SARS-CoV which contains a …

Mechanism and inhibition of the papain‐like protease, PLpro, of SARS‐CoV‐2

T Klemm, G Ebert, DJ Calleja, CC Allison… - The EMBO …, 2020 - embopress.org
The SARS‐CoV‐2 coronavirus encodes an essential papain‐like protease domain as part of
its non‐structural protein (nsp)‐3, namely SARS2 PLpro, that cleaves the viral polyprotein …