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S-Protein-ACE2_paper.pdf (770.55 kB)

In Search for Effective and Safe Drugs Against SARS-CoV-2: Part I] Simulated Interactions Between Selected Nutraceuticals, ACE2 Enzyme and S Protein Simple Peptide Sequences

preprint
submitted on 20.04.2020 and posted on 23.04.2020 by M. Sabry Abdel-Mottaleb, Yousra Abdel-Mottaleb
Coronavirus disease (COVID-19) remains a world pandemic with little treatment options. Nature has provided a plethora of compounds that may offer potential protection and/or treatment choices. Earlier studies have shown a pivotal role of Angiotensin converting enzyme 2 (ACE2) in the pathogenesis of COVID-19. In this context, seven natural compounds were selected and their binding to specific peptide sequences of the coronavirus S-protein: ACE2 interface-drug binding adduct were calculated. Further to the natural drugs, we also similarly examined four well-known antiviral drugs. Moreover, the binding-interface of the isolated coronavirus S-protein and the isolated ACE2 receptor were also individually explored. The identified drug molecules positioned itself achieving geometries of minimum energy resulting in limiting viral recognition of host cells or to disturb host-virus interactions. The frontier orbitals (HOMO-LUMO) play crucial role in the binding interactions of the studied molecules. Most of the drugs act as electron sink whereas the S protein behaves as nucleophile. The results reported pave the way for the identification of small-drug molecule of natural origin with potentially tolerable side effects that can offer protection and/or treatment against coronavirus S-protein COVID-19. Experimental validation is of urgent demand.

Funding

M. S. A. Abdel-Mottaleb and Yousra Abdel-Mottaleb

History

Email Address of Submitting Author

m.s.abdelmottaleb@sci.asu.edu.eg

Institution

Ain Shams University, Faculty of Science, Department of Chemistry

Country

EGYPT

ORCID For Submitting Author

0000-0002-4437-7040

Declaration of Conflict of Interest

No Conflict of Interest

Version Notes

Preliminary

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