Dr Jessica Watt Dr Mathew Martin Professor Jane Endicott Professor Martin Noble
| Different applications and differentiated libraries for crystallographic fragment screening | 2025 |
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Pasquale Morese Ayaz Ahmad Dr Mathew Martin Dr Richard Noble Sara Pintar et al. | Factors affecting irreversible inhibition of EGFR and influence of chirality on covalent binding | 2025 |
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Amy George Frances Sidgwick Dr Jessica Watt Dr Mathew Martin Professor Matthias Trost et al. | Comparison of Quantitative Mass Spectrometric Methods for Drug Target Identification by Thermal Proteome Profiling | 2023 |
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Dr Hannah Stewart Dr Mathew Martin Lan Wang Dr Eilidh Mackenzie Professor Mike Waring et al. | Conformational study into alkyl-aryl ureas to inform drug discovery | 2023 |
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Dr Mathew Martin Professor Jane Endicott Professor Martin Noble Dr Natalie Tatum
| Crystallographic fragment screening in academic cancer drug discovery | 2023 |
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Dr Catherine Salvini Benoit Darlot Jack Davison Dr Mathew Martin Dr Susan Tudhope et al. | Fragment expansion with NUDELs – poised DNA-encoded libraries | 2023 |
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Duncan Miller Dr Suzannah Harnor Dr Mathew Martin Dr Richard Noble Professor Steve Wedge et al. | Modulation of ERK5 Activity as a Therapeutic Anti-Cancer Strategy | 2023 |
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Dr Nahoum Anthony Charlotte Jennings Dr Mathew Martin Dr Richard Noble Nicole Phillips et al. | Targeting cytotoxic agents through EGFR-mediated covalent binding and release | 2023 |
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Dr Jose Luis Marin-Rubio Dr Maria Duenas Fadic Dr Tiaan Heunis Dr Abeer Dannoura Dr Joe Inns et al. | A Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Assay Identifies Nilotinib as an Inhibitor of Inflammation in Acute Myeloid Leukemia | 2022 |
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Melanie Uguen Gemma Davison James Hunter Dr Mathew Martin Dr Shannon Turberville et al. | Build–Couple–Transform: A paradigm for lead-like library synthesis with scaffold diversity | 2022 |
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Dr Mathew Martin Professor Martin Noble
| Exiting the tunnel of uncertainty: crystal soak to validated hit | 2022 |
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Gemma Davison Dr Mathew Martin Dr Shannon Turberville Selma Dormen Dr Richard Heath et al. | Mapping ligand interactions of bromodomains BRD4 and ATAD2 with FragLites and PepLites ─ Halogenated probes of druglike and peptide-like molecular interactions | 2022 |
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Duncan Miller Tristan Reuillon Dr Lauren Molyneux Dr Tim Blackburn Dr Noel Edwards et al. | Parallel Optimization of Potency and Pharmacokinetics Leading to the Discovery of a Pyrrole Carboxamide ERK5 Kinase Domain Inhibitor | 2022 |
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Dr Mathew Martin
| Recent advances in kinase drug discovery part i: The editors’ take | 2021 |
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Gemma Davison Dr Mathew Martin Professor Martin Noble Professor Mike Waring
| Crystallographic and electrophilic fragment screening of the SARS-CoV-2 main protease | 2020 |
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Daniel Wood Svitlana Korolchuk Dr Natalie Tatum Lan Wang Professor Jane Endicott et al. | Differences in the conformational energy landscape of CDK1 and CDK2 suggest a mechanism for achieving selective CDK inhibition | 2019 |
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Daniel Wood Daniel Lopez Fernandez Leanne Knight Islam Al-Khawaldeh Dr Conghao Gai et al. | FragLites - minimal, halogenated fragments displaying pharmacophore doublets. An efficient approach to druggability assessment and hit generation | 2019 |
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Stephanie Myers Duncan Miller Dr Lauren Molyneux Dr Mercedeh Arasta Dr Ruth Bawn et al. | Identification of a novel orally bioavailable ERK5 inhibitor with selectivity over p38α and BRD4 | 2019 |
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Duncan Miller Dr Mathew Martin Santosh Adhikari Alfie Brennan Professor Jane Endicott et al. | Identification of a novel ligand for the ATAD2 bromodomain with selectivity over BRD4 through a fragment growing approach | 2018 |
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Dr Mathew Martin Professor Martin Noble
| Molecular profiling and combinatorial activity of CCT068127: a potent CDK2 and CDK9 inhibitor | 2018 |
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Dr Mathew Martin Dr Helen Lawrence
| Aurora Kinase Inhibitors and methods of making and using thereof | 2017 |
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Christopher Coxon Dr Suzannah Harnor Dr Mathew Martin Dr Benoit Carbain Emeritus Professor Bernard Golding et al. | Cyclin-Dependent Kinase (CDK) Inhibitors; Structure-Activity Relationships and Insights into the CDK-2 Selectivity of 6-Substituted 2-Arylaminopurines | 2017 |
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Dr Mathew Martin
| Structural basis of Wee kinases functionality and inactivation by diverse small molecule inhibitors | 2017 |
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Dr Mathew Martin Professor Jane Endicott Professor Martin Noble
| Structure-based discovery of cyclin-dependent protein kinase inhibitors | 2017 |
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Dr Mathew Martin
| Discovery of Diverse Small-Molecule Inhibitors of Mammalian Sterile20-like Kinase 3 (MST3) | 2016 |
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Svitlana Korolchuk Dr Mathew Martin Dr Will Stanley Professor Martin Noble Professor Jane Endicott et al. | CDK1 structures reveal conserved and unique features of the essential cell cycle CDK | 2015 |
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Elisa Meschini Dr Regina Mora Vidal Dr Mathew Martin Dr Will Stanley Tristan Reuillon et al. | Identification and characterization of an irreversible inhibitor of CDK2 | 2015 |
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Dr Mathew Martin
| Stability of the human Hsp90-p50Cdc37 chaperone complex against nucleotides and Hsp90 inhibitors, and the influence of phosphorylation by casein kinase 2 | 2015 |
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Bailey Massa Dr Mathew Martin Professor Martin Noble Professor Jane Endicott
| Structural and functional characterization of Skp2-containing complexes | 2015 |
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Dr Mathew Martin
| Acetyl-lysine binding site of bromodomain-containing protein 4 (BRD4) interacts with diverse kinase inhibitors | 2014 |
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Dr Mathew Martin Elisa Meschini Lan Wang Dr Regina Mora Vidal Tristan Reuillon et al. | Identification and characterization of an irreversible inhibitor of CDK2 | 2014 |
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