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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|January 22, 2025
Development of compounds for targeted degradation of mammalian cryptochrome proteinsJack Munns, Andrew D Beale, Iacovos N Michaelides, et al.Proceedings of the National Academy of Sciences of the United States of America|October 16, 2021
Changes in selection pressure can facilitate hybridization during biological invasion in a Cuban lizardDan G Bock, Simon Baeckens, Jessica N Pita-Aquino, et al.Bioorganic & Medicinal Chemistry Letters|August 20, 2022
Discovery of a selective c-MET inhibitor with a novel binding modeGavin W Collie, Louise Barlind, Sana Bazzaz, et al.ACS Medicinal Chemistry Letters|December 20, 2023
Rapid PROTAC Discovery Platform: Nanomole-Scale Array Synthesis and Direct Screening of Reaction MixturesMateusz P Plesniak, Emilia K Taylor, Frederik Eisele, et al.Journal of Medicinal Chemistry|March 21, 2024
Optimization of Potent Ligands for the E3 Ligase DCAF15 and Evaluation of Their Use in Heterobifunctional DegradersSimon C C Lucas, Afshan Ahmed, S Neha Ashraf, et al.Journal of Medicinal Chemistry|June 21, 2023
Discovery and Optimization of the First ATP Competitive Type-III c-MET InhibitorIacovos N Michaelides, Gavin W Collie, Ulf Börjesson, et al.Nature Communications|March 25, 2026
A dihydrouracil CRBN ligand mitigates IMiD associated safety liabilities in heterobifunctional targeted protein degraderMonica C Rodrigo-Brenni, Jasper C Komen, Ghaith M Hamza, et al.Pageof 3