Search results (168)
« Back to PublicationsInhibition of MLLT1 limits growth of KMT2A::AFF1 leukaemias without killing healthy haematopoietic stem cells
Journal article
Rajhansa S. et al, (2026), Experimental Hematology, 105458 - 105458
Discovery and Characterization of a Nonacidic Small-Molecule Inhibitor of the Sodium-Coupled Dicarboxylate Transporter NaCT.
Journal article
Quigley A. et al, (2026), Journal of medicinal chemistry
Inhibition of MLLT1 limits growth of MLL-AF4 leukaemias without killing healthy haematopoietic stem cells
Preprint
Rajhansa S. et al, (2025)
Structure-Guided Design of ISOX-DUAL-Based Degraders Targeting BRD4 and CBP/EP300: A Case of Degrader Collapse.
Journal article
Edmonds AK. et al, (2025), Journal of medicinal chemistry, 68, 9638 - 9660
Binding-Site Purification of Actives (B-SPA) Enables Efficient Large-Scale Progression of Fragment Hits by Combining Multi-Step Array Synthesis With HT Crystallography.
Journal article
Grosjean H. et al, (2025), Angewandte Chemie (International ed. in English), 64
Covalent Inhibitors of S100A4 Block the Formation of a Pro-Metastasis Non-Muscle Myosin 2A Complex
Journal article
Giroud C. et al, (2024), Journal of Medicinal Chemistry, 67, 18943 - 18956
Engineered HMGB1 construct with tandem Box B domains promotes tissue regeneration without potential for inflammation
Preprint
Guitart ÁV. et al, (2024)
Enabling equitable and affordable access to novel therapeutics for pandemic preparedness and response via creative intellectual property agreements
Journal article
Griffen EJ. and Boulet P., (2024), Wellcome Open Research, 9, 374 - 374
Unexpected Noncovalent Off-Target Activity of Clinical BTK Inhibitors Leads to Discovery of a Dual NUDT5/14 Antagonist
Journal article
Balıkçı E. et al, (2024), Journal of Medicinal Chemistry, 67, 7245 - 7259
Imidazo[1,2-b]pyridazines as inhibitors of DYRK kinases.
Journal article
Henderson SH. et al, (2024), European journal of medicinal chemistry, 269
Discovery of a Potent, Selective, and Cell-Active SPIN1 Inhibitor.
Journal article
Xiong Y. et al, (2024), Journal of medicinal chemistry, 67, 5837 - 5853
Discovery of PFI-6, a small-molecule chemical probe for the YEATS domain of MLLT1 and MLLT3
Journal article
Raux B. et al, (2024), Bioorganic & Medicinal Chemistry Letters, 98, 129546 - 129546
Open science discovery of potent noncovalent SARS-CoV-2 main protease inhibitors
Journal article
Boby ML. et al, (2023), Science, 382
Turning high-throughput structural biology into predictive inhibitor design
Journal article
Saar KL. et al, (2023), Proceedings of the National Academy of Sciences, 120
Discovery and Development Strategies for SARS-CoV-2 NSP3 Macrodomain Inhibitors
Journal article
Schuller M. et al, (2023), Pathogens, 12, 324 - 324