Abstract
Contact and support
Need help, have a question, or want to contact the ResearchHub team?
© 2026 ResearchHub. Built for responsible scholarly connection.
Scott D. Pegan, David Crich, Ellison Desrochers, Edward B. Starling, Madelyn C. Hansen, Carson Booth, Lauren Nicole Mullininx, Lei Lou, Kuan Y. Chang, Zhong‐Ru Xie
Abstract
Authors
No local reference links have been materialized yet.
No local citing links have been materialized yet.
WHO Declares COVID-19 a Pandemic
2020
10.1016/s1473-3099(20)30120-1
10.1016/s1473-3099(20)30120-1
Mechanism and inhibition of the papain-like protease, PLpro, of SARS-CoV-2
10.15252/embj.2020106275 · 2020
10.1038/s41579-020-00468-6
10.1038/s41579-020-00468-6
10.1016/j.bmcl.2020.127377
10.1016/j.bmcl.2020.127377
Severe acute respiratory syndrome coronavirus 2: from gene structure to pathogenic mechanisms and potential therapy
10.3389/fmicb.2020.01576 · 2020
10.1016/j.antiviral.2014.12.015
10.1016/j.antiviral.2014.12.015
10.1128/jvi.79.24.15189-15198.2005
10.1128/jvi.79.24.15189-15198.2005
Coronavirus protein processing and RNA synthesis is inhibited by the cysteine proteinase inhibitor E64d
10.1006/viro.1995.1123 · 1995
10.1021/acsinfecdis.0c00168
10.1021/acsinfecdis.0c00168
10.1038/s41586-020-2601-5
Institutions
Provenance
crossref
Confidence 100%
ror
Confidence 99%
pubmed
Confidence 98%
europepmc
Confidence 96%
openalex
Confidence 95%
unpaywall
Confidence 95%
doaj
Confidence 92%
datacite
Confidence 0%
10.1038/s41586-020-2601-5
10.1016/j.arcmed.2020.09.013
10.1016/j.arcmed.2020.09.013
10.1126/science.abb3405
10.1126/science.abb3405
Feline coronavirus drug inhibits the main protease of SARS-CoV-2 and blocks virus replication
2020
10.1126/science.abf1611
10.1126/science.abf1611
Unresolved referenced work
Kept as external metadata until matched
Evaluation of green tea polyphenols as novel corona virus (SARS CoV-2) main protease (Mpro) inhibitors–an in silico docking and molecular dynamics simulation study
2020
Identification of polyphenols from Broussonetia papyrifera as SARS CoV-2 main protease inhibitors using in silico docking and molecular dynamics simulation approaches
2020
Identification of dietary molecules as therapeutic agents to combat COVID-19 using molecular docking studies
2020
A dietary molecule as potential anti-COVID-19 agent
2020
Phenol-explorer: an online comprehensive database on polyphenol contents in foods
10.1093/database/bap024 · 2010
10.1021/acs.jctc.5b00864
10.1021/acs.jctc.5b00864
10.1093/nar/28.1.235
10.1093/nar/28.1.235
10.1007/s10822-007-9133-z
10.1007/s10822-007-9133-z
Unresolved referenced work
Kept as external metadata until matched
10.4155/fmc-2016-0093
10.4155/fmc-2016-0093
BindingDB: a web-accessible database of experimentally determined protein-ligand binding affinities
2007
10.1002/jcc.21367
10.1002/jcc.21367
10.1021/acs.jctc.5b00935
10.1021/acs.jctc.5b00935
10.1002/jcc.20945
10.1002/jcc.20945
10.1002/jcc.21287
10.1002/jcc.21287
Cyanidin 3-rutinoside and cyanidin 3-xylosylrutinoside as primary phenolic antioxidants in black raspberry
10.1021/jf072313k · 2008
10.1016/j.bpj.2009.12.4272
10.1016/j.bpj.2009.12.4272
10.1074/jbc.m502577200
10.1074/jbc.m502577200
Critical assessment of the important residues involved in the dimerization and catalysis of MERS Coronavirus Main Protease
2015
10.1016/j.imu.2020.100461
10.1016/j.imu.2020.100461
Both Boceprevir and GC376 efficaciously inhibit SARS-CoV-2 by targeting its main protease
2020
10.1016/s0169-409x(00)00129-0
10.1016/s0169-409x(00)00129-0
Prediction of drug solubility from structure
10.1016/s0169-409x(02)00008-x · 2002
10.1021/cb500917m
10.1021/cb500917m
10.1016/j.compbiomed.2021.104560
10.1016/j.compbiomed.2021.104560 · doi-reference
10.1073/pnas.0805240105
10.1073/pnas.0805240105 · doi-reference
The sugar moiety is a major determinant of the absorption of dietary flavonoid glycosides in man
10.1080/10715769900301141 · doi-reference
10.1002/cbic.201500284
10.1002/cbic.201500284 · doi-reference
Elucidating the inhibitory effect of resveratrol and its structural analogs on selected nucleotide- related enzymes
10.3390/biom10091223 · doi-reference
Frangulosid as a novel hepatitis B virus DNA polymerase inhibitor: a virtual screening study
10.1007/s40203-018-0047-3 · doi-reference
Gram (−) microorganisms DNA polymerase inhibition, antibacterial and chemical properties of fruit and leaf extracts of Sorbus acuparia and Sorbus caucasica var. yaltirikii
10.1002/bmc.3901 · doi-reference
Quercetin nanoparticles display antitumor activity via proliferation inhibition and apoptosis induction in liver cancer cells
10.3892/ijo.2017.3886 · doi-reference
Polyphenols enhance the activity of alkylating agents in leukaemia cell lines
10.18632/oncotarget.27068 · doi-reference
10.1128/jvi.78.20.11334-11339.2004
10.1128/jvi.78.20.11334-11339.2004 · doi-reference
Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction
10.1016/j.antiviral.2006.04.014 · doi-reference
10.1080/14756366.2016.1265519
10.1080/14756366.2016.1265519 · doi-reference
10.1016/j.bmcl.2009.02.010
10.1016/j.bmcl.2009.02.010 · doi-reference
10.1016/j.bmcl.2009.07.009
10.1016/j.bmcl.2009.07.009 · doi-reference
10.1007/s12272-012-0108-9
10.1007/s12272-012-0108-9 · doi-reference
Identification of natural compounds with antiviral activities against SARS-associated coronavirus
10.1016/j.antiviral.2005.02.007 · doi-reference
10.1016/j.jep.2008.03.018
10.1016/j.jep.2008.03.018 · doi-reference
Anti-SARS coronavirus 3C-like protease effects of Isatis indigotica root and plant-derived phenolic compounds
10.1016/j.antiviral.2005.07.002 · doi-reference
Antiviral effects of saikosaponins on human coronavirus 229E in vitro
10.1111/j.1440-1681.2006.04415.x · doi-reference
10.1016/j.bmc.2010.09.035
10.1016/j.bmc.2010.09.035 · doi-reference
10.4103/2225-4110.124335
10.4103/2225-4110.124335 · doi-reference
Inhibition of SARS-CoV 3C-like protease activity by theaflavin-3,3′- digallate (TF3)
10.1093/ecam/neh081 · doi-reference
Medicinal herbal extracts of Sophorae radix, Acanthopanacis cortex, Sanguisorbae radix and Torilis fructus inhibit coronavirus replication in vitro
10.3851/imp1615 · doi-reference
10.1016/j.bmc.2013.03.027
10.1016/j.bmc.2013.03.027 · doi-reference
Resveratrol inhibits rhinovirus replication and expression of inflammatory mediators in nasal epithelia
10.1016/j.antiviral.2015.08.010 · doi-reference
10.1128/jvi.03637-13
10.1128/jvi.03637-13 · doi-reference
10.1128/jvi.05869-11
10.1128/jvi.05869-11 · doi-reference
Resveratrol suppresses nuclear factor-B in herpes simplex virus infected cells
10.1016/j.antiviral.2006.06.011 · doi-reference
Resveratrol as a novel anti-herpes simplex virus nutraceutical agent: an overview
10.3390/v10090473 · doi-reference
Inhibitory effects of resveratrol on the Epstein-Barr virus lytic cycle
10.3390/molecules15107115 · doi-reference
Resveratrol inhibits Epstein Barr Virus lytic cycle in Burkitt’s lymphoma cells by affecting multiple molecular targets
10.1016/j.antiviral.2012.09.003 · doi-reference