Paul E. Brennan, Ph.D.

Affiliations: 
University of Oxford, Oxford, United Kingdom 
Area:
Bio-Organic and Synthetic Chemistry
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Parents

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Paul Allan Bartlett grad student 2000 UC Berkeley
 (I. Phosphinate inhibitors of peptidoglycan biosynthesis. II. Development of a new ring system for combinatorial chemistry.)
Steven Victor Ley post-doc Cambridge

Children

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Milan Mrázek Fowkes research assistant 2015-2016 Oxford
Matthew T O Holland grad student 2020-
David Bowkett grad student 2012-2016 Oxford
Oakley Cox grad student 2012-2016 Oxford
Moses Moustakim grad student 2015-2018 Oxford
Miranda Wright grad student 2015-2018 Oxford
Milan Mrázek Fowkes grad student 2018-2021 Oxford
Mark G McLaughlin post-doc
Joshua Almond-Thynne post-doc 2017-2018 Oxford
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Publications

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Balıkçı E, Marques AMC, Bauer LG, et al. (2024) Unexpected Noncovalent Off-Target Activity of Clinical BTK Inhibitors Leads to Discovery of a Dual NUDT5/14 Antagonist. Journal of Medicinal Chemistry
O'Brien DP, Jones HB, Guenther F, et al. (2023) Structural Premise of Selective Deubiquitinase USP30 Inhibition by Small-Molecule Benzosulfonamides. Molecular & Cellular Proteomics : McP. 100609
Fowkes MM, Troeberg L, Brennan PE, et al. (2023) Development of Selective ADAMTS-5 Peptide Substrates to Monitor Proteinase Activity. Journal of Medicinal Chemistry. 66: 3522-3539
Frank N, Nugent J, Shire BR, et al. (2022) Synthesis of meta-substituted arene bioisosteres from [3.1.1]propellane. Nature
Fowkes MM, Das Neves Borges P, Cacho-Nerin F, et al. (2022) Imaging articular cartilage in osteoarthritis using targeted peptide radiocontrast agents. Plos One. 17: e0268223
De Cesco S, Davis JB, Brennan PE. (2020) TargetDB: A target information aggregation tool and tractability predictor. Plos One. 15: e0232644
Cottone L, Cribbs AP, Khandelwal G, et al. (2020) Inhibition of histone H3K27 demethylases inactivates brachyury (TBXT) and promotes chordoma cell death. Cancer Research
Kahn Tareque R, Hassell-Hart S, Krojer T, et al. (2020) Deliberately Losing Control of C-H Activation Processes in the Design of Small Molecule Fragment Arrays Targeting Peroxisomal Metabolism. Chemmedchem
Ni X, Heidenreich D, Christott T, et al. (2019) Structural Insights into Interaction Mechanisms of Alternative Piperazine-urea YEATS Domain Binders in MLLT1. Acs Medicinal Chemistry Letters. 10: 1661-1666
Fagan V, Johansson C, Gileadi C, et al. (2019) A Chemical Probe for Tudor Domain Protein Spindlin1 to Investigate Chromatin Function. Journal of Medicinal Chemistry
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