Preprint Title Development of QSAR ensemble models for predicting the PAMPA Effective Permeability of new, non-peptidic leads with potential antiviral activity against the coronavirus SARS-CoV-2. Authors

From the onset of the pandemic caused by the virus SARS-CoV-2, the scientific community responded– with a sense of urgency – by intensifying efforts to provide drugs effective against the disease COVID-19. To strengthen this efforts, a consortium of researchers initiated in March 2020 the “COVID Moonshot project” that has been accepting public suggestions for computationally triaged, synthesized, and tested molecules, with experimental data made publicly available. The main goal of the project was to identify through Fragment Based Drug Design (FBDD) small molecules with activity against the virus, for oral treatment. Since orally administered drugs are introduced to the bloodstream through absorption via the small intestine pathway, the ability of a drug to readily cross the intestinal cell membranes and enter circulation is decisively influencing its bioavailability. This explains the need to evaluate and optimize a drug’s membrane permeability in the early stages of drug discovery to avoid failures in latestage drug development owing to incomplete absorption and poor bioavailability. In our present