Publications by authors named "Enbo Yu"

A copper-catalyzed three-component coupling reaction of styrene oxide, aryl iodide, and carbon disulfide for the construction of β-hydroxysulfides has been developed. In this process, readily available CS was used as the sulfur source to construct C-S bonds for the synthesis of phenyl-β-hydroxysulfides and (benzo[]thiazol)-β-hydroxysulfides. This process features mild reaction conditions, simple operation, and wide substrate scope (>50 examples).

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Porcine deltacoronavirus (PDCoV) is an emerging swine enteropathogenic coronavirus that mainly threatens newborn piglets and poses a potential broad cross-species transmission risk. The antigenic epitopes of PDCoV are currently unidentified, and no information about T cell epitopes is available. Here, T-cell epitopes of PDCoV structural proteins were predicted using computational methods.

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Article Synopsis
  • - Porcine deltacoronavirus (PDCoV) is a newly identified coronavirus affecting pigs and poses risks to public health due to its ability to infect various hosts.
  • - Researchers created three monoclonal antibodies (mAbs) to identify neutralizing B-cell epitopes in the virus's S1-CTD protein, with mAb 4E-3 showing effective neutralization and recognizing a specific epitope associated with neutralizing antibody production in mice.
  • - The S epitope, when linked to a carrier protein, not only triggered an immune response in mice and pigs but also offers insights for future PDCoV vaccine development and understanding the virus's pathogenic mechanisms.
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Porcine deltacoronavirus (PDCoV) is highly pathogenic to piglets, and no specific drugs or vaccines are available for the prevention and treatment of PDCoV infection, the need for antiviral therapies is pressing. HSP90 inhibitors have potent inhibitory effects against the replication of numerous viruses, hence we evaluated three HSP90 inhibitors, 17-AAG, VER-82576, and KW-2478, for their effects on PDCoV infection in vitro. We evaluated their effectivenesses at suppressing PDCoV by qRT-PCR, western blot, and TCID assay, and found that 17-AAG and VER-82576 inhibited PDCoV at the early stage of replication, while KW-2478 showed no significant antiviral activity at any stage of infection.

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