IN SILICON EVALUATION OF ARTEMISININ DERIVATIVES AS POTENTIAL INHIBITORS OF SARS-COV-2 MAIN PROTEASE
Four artemisinin-derived compounds namely, artesunate, artemether, artemisinin and dihydroartemisinin were evaluated as potential Mpro binders using molecular docking and post docking interaction analysis and among the tested ligands, artesunate showed the most favorable predicted binding affinity with docking score.