22 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Optimization, and biological evaluation of 3-O-β-chacotriosyl betulinic acid amide derivatives as novel small-molecule Omicron.

South China Agricultural University
C-2 Thiophenyl Tryptophan Trimers Inhibit Cellular Entry of SARS-CoV-2 through Interaction with the Viral Spike (S) Protein.

Instituto De Quimica Medica (IQM)
design of a stapled peptide targeting SARS-CoV-2 spike protein receptor-binding domain.

Kansas State University
Inhibitors of SARS-CoV-2 Entry: Current and Future Opportunities.

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

Peking Union Medical College
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 α-glucosidase and SARS-CoV-2 entry inhibitors.

Zhengzhou University
Identification, optimization, and biological evaluation of 3-O-β-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
Discovery and structural optimization of 3-O-β-chacotriosyl oleanane-type triterpenoids as potent entry inhibitors of SARS-CoV-2 virus infections.

South China Agricultural University
Druggable targets from coronaviruses for designing new antiviral drugs.

Federal University of Alagoas
FUSED POLYCYCLIC SUBSTITUTED 5-CARBOXYLIC ACID THIENOPYRIMIDINE DIONE COMPOUND AND USE THEREOF

Soter Biopharma
LSD1 inhibitor and preparation method and application thereof

Medshine Discovery
3-hydroxy-quinazoline-2,4-dione derivatives and their use as nuclease modulators

Ludwig Institute For Cancer Research
Thiazolidinone compounds and use thereof

National Health Research Institute