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Proceedings of the National Academy of Sciences of the United States of America|May 23, 2014
Prokaryotic NavMs channel as a structural and functional model for eukaryotic sodium channel antagonismClaire Bagnéris, Paul G DeCaen, Claire E Naylor, et al.Chemical Communications (Cambridge, England)|January 13, 2012
New lithium-zincate approaches for the selective functionalisation of pyrazine: direct dideprotozincation vs. nucleophilic alkylationSharon E Baillie, Victoria L Blair, David C Blakemore, et al.Nature|August 25, 2016
Structural basis for inhibition of a voltage-gated Ca2+ channel by Ca2+ antagonist drugsLin Tang, Tamer M Gamal El-Din, Teresa M Swanson, et al.Bioorganic & Medicinal Chemistry Letters|October 12, 2010
An in situ oxidation strategy towards overcoming hERG affinityDavid C Pryde, Rhys Jones, Donald S Middleton, et al.Antimicrobial Agents and Chemotherapy|April 20, 2011
Selection, optimization, and pharmacokinetic properties of a novel, potent antiviral locked nucleic acid-based antisense oligomer targeting hepatitis C virus internal ribosome entry siteCarl Laxton, Kevin Brady, Sterghios Moschos, et al.Proceedings of the National Academy of Sciences of the United States of America|December 12, 2019
Valproic acid interactions with the NavMs voltage-gated sodium channelGeancarlo Zanatta, Altin Sula, Andrew J Miles, et al.Proceedings of the National Academy of Sciences of the United States of America|November 16, 2018
TRPA1 ankyrin repeat six interacts with a small molecule inhibitor chemotypeWei Chou Tseng, David C Pryde, Katrina E Yoger, et al.Nucleosides, Nucleotides & Nucleic Acids|October 2, 2013
Synthesis and biological evaluation of acyclic phosphonic acid nucleoside derivativesPhilip Wainwright, Adrian Maddaford, Xiurong Zhang, et al.Molecular Pharmaceutics|October 6, 2016
Analysis of Differential Efficacy and Affinity of GABAA (α1/α2) Selective ModulatorsQurrat U Ain, Robert M Owen, Kiyoyuki Omoto, et al.Journal of Medicinal Chemistry|November 8, 2007
Cyclization of the acyl glucuronide metabolite of a neutral endopeptidase inhibitor to an electrophilic glutarimide: synthesis, reactivity, and mechanistic analysisXiaoli Meng, James L Maggs, David C Pryde, et al.Pageof 5