P
Paul Bamborough
Researcher at GlaxoSmithKline
Publications - 89
Citations - 4676
Paul Bamborough is an academic researcher from GlaxoSmithKline. The author has contributed to research in topics: Bromodomain & Kinase. The author has an hindex of 33, co-authored 86 publications receiving 3998 citations.
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Patent
Benzimidazol substituted thiopene derivatives with atctivity on ikk3
Paul Bamborough,James V. Morey +1 more
TL;DR: The benzimidazole derivatives are potentially useful in the treatment of diseases associated with inappropriate I-kappa-B kinase-3 (IKK3) as discussed by the authors.
Journal ArticleDOI
Optimization of Potent ATAD2 and CECR2 Bromodomain Inhibitors with an Atypical Binding Mode
Simon C. C. Lucas,Stephen John Atkinson,Paul Bamborough,Heather A. Barnett,Chun-wa Chung,Laurie J. Gordon,Darren Jason Mitchell,Alexander N Phillipou,Rab K. Prinjha,Robert J. Sheppard,Nicholas C. O. Tomkinson,Robert J. Watson,Emmanuel Hubert Demont +12 more
TL;DR: The optimisation of a series of phenyl sulfonamides which exhibit a novel mode of binding to non-Bromodomain and Extra Terminal Domain (non-BET) bromidomains through displacement of a normally conserved network of four water molecules is reported.
Journal ArticleDOI
CDK12 inhibition reduces abnormalities in cells from patients with myotonic dystrophy and in a mouse model.
Ami Ketley,Marzena Wojciechowska,Sonja Ghidelli-Disse,Paul Bamborough,Tushar K. Ghosh,Marta Lopez Morato,Saam Sedehizadeh,Naveed Altaf Malik,Zhen Zhi Tang,Paulina K. Powalowska,Matthew K Tanner,Rudolf Billeter-Clark,Rebecca C. Trueman,Philippine C. Geiszler,Alessandra Agostini,Othman Ahmad Othman,Markus Bösche,Marcus Bantscheff,Martin Rüdiger,Danuta E. Mossakowska,Danuta E. Mossakowska,David H. Drewry,William J. Zuercher,William J. Zuercher,Charles A. Thornton,Gerard Drewes,Iain Uings,Christopher J. Hayes,J. David Brook +28 more
TL;DR: Small-molecule inhibitors that remove nuclear foci and have beneficial effects in the HSALR mouse model, reducing transgene expression, leading to improvements in myotonia, splicing, and centralized nuclei are reported.
Patent
Nicotinamide Derivatives Useful as p38 Inhibitors
TL;DR: The p38 inhibitors of formula (I) are inhibitors of p38 kinase and are useful in the treatment of conditions or disease states mediated by p38 activity or mediated by cytokines produced by the activity of P38 as discussed by the authors.
Journal ArticleDOI
The Discovery of Novel Antimalarial Aminoxadiazoles as a Promising Nonendoperoxide Scaffold
Elena Sandoval,Maria Jose Lafuente-Monasterio,Maria Jesus Almela,Pablo Castañeda,María Belén Jiménez Díaz,Maria Santos Martinez-Martinez,J. Vidal,Iñigo Angulo-Barturen,Paul Bamborough,Jeremy N. Burrows,Nicholas Cammack,María J. Chaparro,Jose M. Coteron,Cristina de Cozar,Benigno Crespo,Beatriz Hernández Díaz,Gerard Drewes,Esther Fernández,Santiago Ferrer-Bazaga,María T. Fraile,Francisco J. Gamo,Sonja Ghidelli-Disse,Rubén M. Gómez,John N. Haselden,Sophie Huss,María Luisa León,Jaime de Mercado,Simon J. F. Macdonald,Jose Ignacio Martin Hernando,Sara Prats,Margarita Puente,Anne Rodríguez,Juan C. de la Rosa,Lourdes Rueda,Carolyn Selenski,Paul Willis,David Matthew Wilson,Michael J Witty,Félix Calderón +38 more
TL;DR: An aminoxadiazole with an antiparasitic profile comparable with artemisinin is identified from the GSK antimalarial set, with no cross-resistance in a resistant strains panel and a potential new mode of action.