PMID

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Article Title

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Clofazimine derivatives as potent broad-spectrum antiviral agents with dual-target mechanism.

Peking Union Medical College and Chinese Academy of Medical Sciences

Target-Based Virtual Screening and LC/MS-Guided Isolation Procedure for Identifying Phloroglucinol-Terpenoid Inhibitors of SARS-CoV-2.

Kunming Institute of Botany

Discovery of honokiol thioethers containing 1,3,4-oxadiazole moieties as potential ?-glucosidase and SARS-CoV-2 entry inhibitors.

Zhengzhou University

Identification, optimization, and biological evaluation of 3-O-?-chacotriosyl ursolic acid derivatives as novel SARS-CoV-2 entry inhibitors by targeting the prefusion state of spike protein.

South China Agricultural University

Synthesis of low-molecular weight fucoidan derivatives and their binding abilities to SARS-CoV-2 spike proteins.

Keio University

Natural Products with Potential to Treat RNA Virus Pathogens Including SARS-CoV-2.

University of California San Diego

Synthetic Peptides That Antagonize the Angiotensin-Converting Enzyme-2 (ACE-2) Interaction with SARS-CoV-2 Receptor Binding Spike Protein.

University of Groningen

Identification of a dual acting SARS-CoV-2 proteases inhibitor through in silico design and step-by-step biological characterization.

University of Salerno

Stapled Peptides Targeting SARS-CoV-2 Spike Protein HR1 Inhibit the Fusion of Virus to Its Cell Receptor.

Second Military Medical University

Computational Design of Potent D-Peptide Inhibitors of SARS-CoV-2.

University of Toronto

Colloidal Aggregators in Biochemical SARS-CoV-2 Repurposing Screens.

University of California San Francisco (Ucsf)

Axial Chiral Binaphthoquinone and Perylenequinones from the Stromata of

Chinese Academy of Sciences