Publication date: Jan 16, 2025
The global impact of SARS-CoV-2 highlights the need for treatments beyond vaccination, given the limited availability of effective medications. While Pfizer introduced Paxlovid, an FDA-approved antiviral targeting the SARS-CoV-2 main protease (Mpro), this study focuses on designing new antivirals against another protease, papain-like protease (PLpro), which is crucial for viral replication and immune suppression. NCATS/NIH performed a high-throughput screen of ∼15,000 molecules from an internal molecular library, identifying initial hits with a 0. 5% success rate. To improve the hit rate and identify potent inhibitors, machine learning-based virtual screens were applied to ∼150,000 compounds, yielding 125 top predicted hits. Biochemical evaluation revealed 25 promising compounds, with a 20% hit-rate and IC values from 1. 75 μM to
Concepts | Keywords |
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Antiviral | Compounds |
Fda | Cov |
Library | Global |
Promising | Highlights |
Hit | |
Hits | |
Inhibitors | |
Learning | |
Limited | |
Plpro | |
Protease | |
Rate | |
Sars | |
Treatments | |
Vaccination |
Semantics
Type | Source | Name |
---|---|---|
drug | DRUGBANK | Papain |
pathway | KEGG | Viral replication |
drug | DRUGBANK | Spinosad |