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Open AccessStructure-based design of pan-coronavirus inhibitors targeting host cathepsin L and calpain-1
Respiratory disease caused by coronavirus infection remains a global health crisis. Although several SARS-CoV-2-specific vaccines and direct-acting antivirals are available, their efficacy on emerging coronavi...
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Open AccessStructure-based discovery of dual pathway inhibitors for SARS-CoV-2 entry
Since 2019, SARS-CoV-2 has evolved rapidly and gained resistance to multiple therapeutics targeting the virus. Development of host-directed antivirals offers broad-spectrum intervention against different varia...
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Open AccessCorrection: Discovery of novel non-peptidic and non-covalent small-molecule 3CLpro inhibitors as potential candidate for COVID-19 treatment
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Open AccessStructure-based development and preclinical evaluation of the SARS-CoV-2 3C-like protease inhibitor simnotrelvir
The persistent pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its variants accentuates the great demand for develo** effective ther...
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Open AccessA viral RNA-dependent RNA polymerase inhibitor VV116 broadly inhibits human coronaviruses and has synergistic potency with 3CLpro inhibitor nirmatrelvir
During the ongoing pandemic, providing treatment consisting of effective, low-cost oral antiviral drugs at an early stage of SARS-CoV-2 infection has been a priority for controlling COVID-19. Although Paxlovid...
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Open AccessDiscovery of novel non-peptidic and non-covalent small-molecule 3CLpro inhibitors as potential candidate for COVID-19 treatment
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Research on rub-impact rotor vibration of hydraulic generating set based on HB-AFT method
Under the combined effects of electromagnetic and mechanical excitation, the strong nonlinear and discontinuous characteristics are presented within differential equations of rotor-bearing system for hydraulic...
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Open AccessCorrection to: Novel and potent inhibitors targeting DHODH are broad-spectrum antivirals against RNA viruses including newly-emerged coronavirus SARS-CoV-2
In the original publication the author’s name ‘Dimitri Lavillete’ is published incorrectly. The correct author name should be spelt as ‘Dimitri Lavillette’ is provided in this correction.
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Open AccessCrystal structure of SARS-CoV-2 main protease in complex with protease inhibitor PF-07321332
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Open AccessEbola virus VP35 hijacks the PKA-CREB1 pathway for replication and pathogenesis by AKIP1 association
Ebola virus (EBOV), one of the deadliest viruses, is the cause of fatal Ebola virus disease (EVD). The underlying mechanism of viral replication and EBOV-related hemorrhage is not fully understood. Here, we sh...
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Open AccessOral remdesivir derivative VV116 is a potent inhibitor of respiratory syncytial virus with efficacy in mouse model
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Open AccessCoVac501, a self-adjuvanting peptide vaccine conjugated with TLR7 agonists, against SARS-CoV-2 induces protective immunity
Safe, effective, and economical vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are needed to achieve adequate herd immunity and end the pandemic. We constructed a novel SARS-CoV-...
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Open AccessDesign and development of an oral remdesivir derivative VV116 against SARS-CoV-2
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Open AccessHigh-throughput screening identifies established drugs as SARS-CoV-2 PLpro inhibitors
A new coronavirus (SARS-CoV-2) has been identified as the etiologic agent for the COVID-19 outbreak. Currently, effective treatment options remain very limited for this disease; therefore, there is an urgent n...
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Open AccessIdentification of pyrogallol as a warhead in design of covalent inhibitors for the SARS-CoV-2 3CL protease
The ongoing pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) urgently needs an effective cure. 3CL protease (3CLpro) is a highly conserved cys...
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Open AccessIdentification of proteasome and caspase inhibitors targeting SARS-CoV-2 Mpro
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Open AccessInhibition mechanism of SARS-CoV-2 main protease by ebselen and its derivatives
The SARS-CoV-2 pandemic has triggered global efforts to develop therapeutics. The main protease of SARS-CoV-2 (Mpro), critical for viral replication, is a key target for therapeutic development. An organoselenium...
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Structural basis for inhibition of the SARS-CoV-2 RNA polymerase by suramin
The COVID-19 pandemic caused by nonstop infections of SARS-CoV-2 has continued to ravage many countries worldwide. Here we report that suramin, a 100-year-old drug, is a potent inhibitor of the SARS-CoV-2 RNA-...
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Open AccessCorrection to: Novel and potent inhibitors targeting DHODH are broad-spectrum antivirals against RNA viruses including newly-emerged coronavirus SARS-CoV-2
In the original publication there are few errors in Figure 1. The correct Figure 1 is provided in this correction
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Comparative Antiviral Efficacy of Viral Protease Inhibitors against the Novel SARS-CoV-2 In Vitro
The recent outbreak of novel coronavirus pneumonia (COVID-19) caused by a new coronavirus has posed a great threat to public health. Identifying safe and effective antivirals is of urgent demand to cure the hu...