Abstract Title:

Identification of bioactive molecule from(Ashwagandha) as SARS-CoV-2 main protease inhibitor.

Abstract Source:

J Biomol Struct Dyn. 2020 Jul 8:1-14. Epub 2020 Jul 8. PMID: 32643552

Abstract Author(s):

Manish Kumar Tripathi, Pushpendra Singh, Sujata Sharma, Tej P Singh, A S Ethayathulla, Punit Kaur

Article Affiliation:

Manish Kumar Tripathi


SARS-CoV-2 is the causative agent of COVID-19 and has been declared as pandemic disease by World Health Organization. Lack of targeted therapeutics and vaccines for COVID-2019 have triggered the scientific community to develop new vaccines or drugs against this novel virus. Many synthetic compounds and antimalarial drugs are undergoing clinical trials. The traditional medical practitioners widely use Indian medicinal plant(Ashwagandha) natural constituents, called withanolides for curing various diseases. The main protease (M) of SARS-CoV-2 plays a vital role in disease propagation by processing the polyproteins which are required for its replication. Hence, it denotes a significant target for drug discovery. In the present study, we evaluate the potential of 40 natural chemical constituents of Ashwagandha to explore a possible inhibitor against main protease of SARS-CoV-2 by adopting the computational approach. The docking study revealed that four constituents of Ashwagandha; Withanoside II (-11.30 Kcal/mol), Withanoside IV (-11.02 Kcal/mol), Withanoside V (-8.96 Kcal/mol) and Sitoindoside IX (-8.37 Kcal/mol) exhibited the highest docking energy among the selected natural constituents. Further, MD simulation study of 100 ns predicts Withanoside V possess strong binding affinity andhydrogen-bonding interactions with the protein active site and indicates its stability in the active site. The binding free energy score also correlates with the highest score of -87.01 ± 5.01 Kcal/mol as compared to other selected compounds. In conclusion, our study suggests that WithanosideV in Ashwagandha may be serve as a potential inhibitor against Mof SARS-CoV-2 to combat COVID-19 and may have an antiviral effect on nCoV. Communicated by Ramaswamy H. Sarma.

Study Type : In Vitro Study

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