Integrated computational screen and validation of thalidomide-based PROTACs targeting SARS-CoV-2 main protease
Abstract
Three novel thalidomide-based PROTACs (A, B, and C) demonstrate efficient binding to and degradation of SARS-CoV-2 M pro in transfected HEK293 cells with high selectivity, mediated through the ubiquitin–proteasome system.
Fields of Study & Subjects
Protein Degradation and Inhibitors
Chromatin Remodeling and Cancer
PARP inhibition in cancer therapy
Publication details
- Journal / source
- RSC Medicinal Chemistry
- Publisher
- Royal Society of Chemistry (RSC)
- Volume
- 17
- Issue
- 2
- Pages
- 1135–1143
- Publication date
- 1 January 2026
- Language
- EN