MedicineChemistryEnvironmental Science

Muhammad Tahir ul Qamar, Safar M. Alqahtani, M. Alamri, Lingling Chen

2020.2.14Journal of Pharmaceutical Analysis

DOI: 10.1016/j.jpha.2020.03.009

tlooto Summary

Analysis of the 3CLpro sequence, constructed its 3D homology model, and screened it against a medicinal plant library containing 32,297 potential anti-viral phytochemicals/traditional Chinese medicinal compounds revealed that the top nine hits might serve as potential anti- SARS-CoV-2 lead molecules for further optimisation and drug development process to combat COVID-19.

Abstract

The recent pandemic of coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2 has raised global health concerns. The viral 3-chymotrypsin-like cysteine protease (3CLpro) enzyme controls coronavirus replication and is essential for its life cycle. 3CLpro is a proven drug discovery target in the case of severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV). Recent studies revealed that the genome sequence of SARS-CoV-2 is very similar to that of SARS-CoV. Therefore, herein, we analysed the 3CLpro sequence, constructed its 3D homology model, and screened it against a medicinal plant library containing 32,297 potential anti-viral phytochemicals/traditional Chinese medicinal compounds. Our analyses revealed that the top nine hits might serve as potential anti- SARS-CoV-2 lead molecules for further optimisation and drug development process to combat COVID-19.

Citation format

QAMAR, Muhammad Tahir ul, et al. Structural basis of SARS-CoV-2 3clpro and anti-covid-19 drug discovery from medicinal plants. Journal of Pharmaceutical Analysis, 2020, 10: 313–319.