4.4 Article

Small Molecule Inhibitors of Middle East Respiratory Syndrome Coronavirus Fusion by Targeting Cavities on Heptad Repeat Trimers

Journal

BIOMOLECULES & THERAPEUTICS
Volume 28, Issue 4, Pages 311-319

Publisher

KOREAN SOC APPLIED PHARMACOLOGY
DOI: 10.4062/biomolther.2019.202

Keywords

MERS-CoV; Antiviral agents; Virtual screening; Plaques inhibition

Funding

  1. Deanship of Scientific Research at King Faisal University under Strategic projects track [171001]
  2. National Research Foundation - Ministry of Science and ICT in the Republic of Korea [2016M3A9B6916708]
  3. Ministry of Education, Culture, Sports, Science, and Technology, Japan [16H06575]
  4. Japan Society for the Promotion of Science [18K15235, 16H06276]
  5. Japan Agency for Medical Research and Development (AMED) [Program of Japan Initiative for Global Research Network on Infectious Diseases (JGRID)] [JP18fm0108006]
  6. Grants-in-Aid for Scientific Research [16H06575, 18K15235] Funding Source: KAKEN
  7. National Research Foundation of Korea [2016M3A9B6916708] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Middle East Respiratory Syndrome Coronavirus (MERS-CoV) is a newly emerging viral disease with fatal outcomes. However, no MERS-CoV-specific treatment is commercially available. Given the absence of previous structure-based drug discovery studies targeting MERS-CoV fusion proteins, this set of compounds is considered the first generation of MERS-CoV small molecule fusion inhibitors. After a virtual screening campaign of 1.56 million compounds followed by cell-cell fusion assay and MERS-CoV plaques inhibition assay, three new compounds were identified. Compound numbers 22, 73, and 74 showed IC50 values of 12.6, 21.8, and 11.12 mu M, respectively, and were most effective at the onset of spike-receptor interactions. The compounds exhibited safe profiles against Human embryonic kidney cells 293 at a concentration of 20 mu M with no observed toxicity in Vero cells at 10 mu M. The experimental results are accompanied with predicted favorable pharmacokinetic descriptors and drug-likeness parameters. In conclusion, this study provides the first generation of MERS-CoV fusion inhibitors with potencies in the low micromolar range.

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