In silico molecular docking and molecular dynamics examination of Andrographis paniculata compounds of Andrographolide, Neoandrographolide, and 5-hydroxy-7,8,2’,3’-tetramethoxyflavone inhibition activity to SARS-CoV-2 main protease

¹ Department of Metallurgical and Materials Engineering, Faculty of Engineering, University of Indonesia, Depok, Jawa Barat, Indonesia, 16424
² Department of Medicine Chemistry, Faculty of Medicine, University of Indonesia, Salemba, Jakarta, Indonesia, 10430
³ Department of Physics, Faculty of Mathematics and Natural Sciences, Universitas Negeri Semarang, Semarang 50229

^* Corresponding author: jakafajar@ui.ac.id

Abstract

In this work, Andrographis paniculata compounds of Andrographolide, Neoandrographolide, and 5-hydroxy-7,8,2’,3’-tetramethoxyflavone inhibition activity to SARS CoV-2 main protease were examined through in silico molecular docking and molecular dynamics simulation, with Remdesivir as control ligand. Docking score and MMGBSA were examined as well as molecular dynamics parameters: RMSD, RMSF and Protein ligand contact fraction. Our study found that Andrographis paniculata compounds of Andrographolide, Neoandrographolide, and 5-hydroxy-7,8,2’,3’-tetramethoxyflavone have comparable inhibition activity to SARS CoV-2 main protease in comparison to Remdesivir. 5-hydroxy7,8,2’,3’-tetramethoxyflavone has the lowest docking score, which was further validated by protein ligand contact fraction examination, although MMGBSA score is lowest for Remdesivir.