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Catalytic meta-selective CH functionalization to construct quaternary carbon centres
N Press, A Paterson, S John-Campbell, M Mahon, C Frost
Chemical Communications 51 (64), 2015
1632015
Catalytic meta-selective C–H functionalization to construct quaternary carbon centres
AJ Paterson, S St John-Campbell, MF Mahon, NJ Press, CG Frost
Chemical Communications 51 (64), 12807-12810, 2015
163*2015
An inhibitor of NADPH oxidase-4 attenuates established pulmonary fibrosis in a rodent disease model
ER Jarman, VS Khambata, C Cope, P Jones, J Roger, LY Ye, N Duggan, ...
American journal of respiratory cell and molecular biology 50 (1), 158-169, 2014
1262014
Dual PDE3/4 inhibitors as therapeutic agents for chronic obstructive pulmonary disease
KH Banner, NJ Press
British journal of pharmacology 157 (6), 892-906, 2009
1152009
Characterization of cigarette smoke-induced inflammatory and mucus hypersecretory changes in rat lung and the role of CXCR2 ligands in mediating this effect
CS Stevenson, K Coote, R Webster, H Johnston, HC Atherton, A Nicholls, ...
American Journal of Physiology-Lung Cellular and Molecular Physiology 288 (3 …, 2005
1092005
A common intracellular allosteric binding site for antagonists of the CXCR2 receptor
K Salchow, ME Bond, SC Evans, NJ Press, SJ Charlton, PA Hunt, ...
British journal of pharmacology 159 (7), 1429-1439, 2010
882010
2 PDE4 inhibitors–a review of the current field
NJ Press, KH Banner
Progress in medicinal chemistry 47, 37-74, 2009
812009
Heparin-steroid conjugates: new angiogenesis inhibitors with antitumor activity in mice
PE Thorpe, EJ Derbyshire, SP Andrade, N Press, PP Knowles, S King, ...
Cancer research 53 (13), 3000-3007, 1993
811993
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
α-Halo carbonyls enable meta selective primary, secondary and tertiary C–H alkylations by ruthenium catalysis
AJ Paterson, CJ Heron, CL McMullin, MF Mahon, NJ Press, CG Frost
Organic & biomolecular chemistry 15 (28), 5993-6000, 2017
502017
The Crystalline Sponge Method: A Systematic Study of the Reproducibility of Simple Aromatic Molecule Encapsulation and Guest–Host Interactions
LM Hayes, CE Knapp, KY Nathoo, NJ Press, DA Tocher, CJ Carmalt
Crystal Growth & Design 16 (6), 3465-3472, 2016
442016
Synthesis of a Protected (±)-Calicheamicinone Derivative by Sequential Introduction of Functionality into the Bicyclo [7.3. 1] enediyne Core Structure
P Magnus, GF Miknis, NJ Press, D Grandjean, GM Taylor, J Harling
Journal of the American Chemical Society 119 (29), 6739-6748, 1997
411997
Targeting the serotonin pathway for the treatment of pulmonary arterial hypertension
M Thomas, L Ciuclan, MJ Hussey, NJ Press
Pharmacology & therapeutics 138 (3), 409-417, 2013
392013
A new orally bioavailable dual adenosine A2B/A3 receptor antagonist with therapeutic potential
NJ Press, RJ Taylor, JD Fullerton, P Tranter, C McCarthy, TH Keller, ...
Bioorganic & medicinal chemistry letters 15 (12), 3081-3085, 2005
382005
Aminothaizoles and their use as adenosine receptor antagonists
NJ Press, RJ Taylor
US Patent 7,109,202, 2006
372006
CGH2466, a combined adenosine receptor antagonist, p38 mitogen‐activated protein kinase and phosphodiesterase type 4 inhibitor with potent in vitro and in vivo anti …
A Trifilieff, TH Keller, NJ Press, T Howe, P Gedeck, D Beer, C Walker
British journal of pharmacology 144 (7), 1002-1010, 2005
342005
Solubility-driven optimization of phosphodiesterase-4 inhibitors leading to a clinical candidate
NJ Press, RJ Taylor, JD Fullerton, P Tranter, C McCarthy, TH Keller, ...
Journal of medicinal chemistry 55 (17), 7472-7479, 2012
312012
Therapeutic potential of adenosine receptor antagonists and agonists
NJ Press, S Gessi, PA Borea, R Polosa
Expert opinion on therapeutic patents 17 (8), 979-991, 2007
292007
The discovery of potent, orally bioavailable pyrazolo and triazolopyrimidine CXCR2 receptor antagonists
DW Porter, M Bradley, Z Brown, R Canova, S Charlton, B Cox, P Hunt, ...
Bioorganic & medicinal chemistry letters 24 (1), 72-76, 2014
272014
The discovery of potent, orally bioavailable pyrimidine-5-carbonitrile-6-alkyl CXCR2 receptor antagonists
DW Porter, M Bradley, Z Brown, SJ Charlton, B Cox, P Hunt, D Janus, ...
Bioorganic & medicinal chemistry letters 24 (15), 3285-3290, 2014
252014
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