Követés
Stephen Roughley
Stephen Roughley
Vernalis Research
E-mail megerősítve itt: vernalis.com
Cím
Hivatkozott rá
Hivatkozott rá
Év
The medicinal chemist’s toolbox: an analysis of reactions used in the pursuit of drug candidates
SD Roughley, AM Jordan
Journal of medicinal chemistry 54 (10), 3451-3479, 2011
24162011
4, 5-diarylisoxazole Hsp90 chaperone inhibitors: potential therapeutic agents for the treatment of cancer
PA Brough, W Aherne, X Barril, J Borgognoni, K Boxall, JE Cansfield, ...
Journal of medicinal chemistry 51 (2), 196-218, 2008
5062008
Novel, potent small-molecule inhibitors of the molecular chaperone Hsp90 discovered through structure-based design
BW Dymock, X Barril, PA Brough, JE Cansfield, A Massey, E McDonald, ...
Journal of medicinal chemistry 48 (13), 4212-4215, 2005
2752005
Combining Hit Identification Strategies: Fragment-Based and in Silico Approaches to Orally Active 2-Aminothieno[2,3-d]pyrimidine Inhibitors of the Hsp90 Molecular …
PA Brough, X Barril, J Borgognoni, P Chene, NGM Davies, B Davis, ...
Journal of medicinal chemistry 52 (15), 4794-4809, 2009
1902009
Drug-like annotation and duplicate analysis of a 23-supplier chemical database totalling 2.7 million compounds
N Baurin, R Baker, C Richardson, I Chen, N Foloppe, A Potter, A Jordan, ...
Journal of chemical information and computer sciences 44 (2), 643-651, 2004
1752004
Synthesis of (−)-Histrionicotoxin by a Tandem Process
GM Williams, SD Roughley, JE Davies, AB Holmes, JP Adams
Journal of the American Chemical Society 121 (20), 4900-4901, 1999
1211999
How well can fragments explore accessed chemical space? A case study from heat shock protein 90: miniperspective
SD Roughley, RE Hubbard
Journal of medicinal chemistry 54 (12), 3989-4005, 2011
1072011
Dynamic undocking and the quasi-bound state as tools for drug discovery
S Ruiz-Carmona, P Schmidtke, FJ Luque, L Baker, N Matassova, B Davis, ...
Nature chemistry 9 (3), 201-206, 2017
882017
Hsp90 inhibitors and drugs from fragment and virtual screening
S Roughley, L Wright, P Brough, A Massey, RE Hubbard
Fragment-Based Drug Discovery and X-Ray Crystallography, 61-82, 2011
74*2011
Off-rate screening (ORS) by surface plasmon resonance. An efficient method to kinetically sample hit to lead chemical space from unpurified reaction products
JB Murray, SD Roughley, N Matassova, PA Brough
Journal of medicinal chemistry 57 (7), 2845-2850, 2014
702014
Nitrone dipolar cycloaddition routes to piperidines and indolizidines. Part 9. Formal synthesis of (−)-pinidine and total synthesis of (−)-histrionicotoxin,(+)-histrionicotoxin …
EC Davison, ME Fox, AB Holmes, SD Roughley, CJ Smith, GM Williams, ...
Journal of the Chemical Society, Perkin Transactions 1, 1494-1514, 2002
652002
Targeting conserved water molecules: design of 4-aryl-5-cyanopyrrolo [2, 3-d] pyrimidine Hsp90 inhibitors using fragment-based screening and structure-based optimization
NGM Davies, H Browne, B Davis, MJ Drysdale, N Foloppe, S Geoffrey, ...
Bioorganic & medicinal chemistry 20 (22), 6770-6789, 2012
482012
Drug discovery chemistry: a primer for the non-specialist
AM Jordan, SD Roughley
Drug discovery today 14 (15-16), 731-744, 2009
482009
Establishing drug discovery and identification of hit series for the anti-apoptotic proteins, Bcl-2 and Mcl-1
JB Murray, J Davidson, I Chen, B Davis, P Dokurno, CJ Graham, R Harris, ...
ACS omega 4 (5), 8892-8906, 2019
472019
Structure-based design of agents targeting the bacterial ribosome
J Bower, M Drysdale, R Hebdon, A Jordan, G Lentzen, N Matassova, ...
Bioorganic & medicinal chemistry letters 13 (15), 2455-2458, 2003
452003
Fatty acid amide hydrolase inhibitors. Surprising selectivity of chiral azetidine ureas
T Hart, AT Macias, K Benwell, T Brooks, J D’Alessandro, P Dokurno, ...
Bioorganic & medicinal chemistry letters 19 (15), 4241-4244, 2009
442009
Design and Synthesis of 56 Shape‐Diverse 3D Fragments
TD Downes, SP Jones, HF Klein, MC Wheldon, M Atobe, PS Bond, ...
Chemistry (Weinheim an der Bergstrasse, Germany) 26 (41), 8969, 2020
412020
Fragment-based lead discovery
BJ Davis, SD Roughley
Annual reports in medicinal chemistry 50, 371-439, 2017
342017
Application of off-rate screening in the identification of novel pan-isoform inhibitors of pyruvate dehydrogenase kinase
PA Brough, L Baker, S Bedford, K Brown, S Chavda, V Chell, ...
Journal of Medicinal Chemistry 60 (6), 2271-2286, 2017
282017
Thioesterification and selenoesterification of amides via selective N–C cleavage at room temperature: N–C (O) to S/Se–C (O) interconversion
MM Rahman, G Li, M Szostak
Synthesis 52 (07), 1060-1066, 2020
212020
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