Barry V. L. Potter, MA DPhil DSc FRSB FRSC MAE FMedSci

Max-Planck-Institute for Experimental Medicine, Göttingen, Germany 
 1984-1990 Biological Chemistry University of Leicester, Leicester, England, United Kingdom 
 1990- Medicine & Biological Chemistry University of Bath, Bath, England, United Kingdom 
 1998-2010 Sterix Ltd. 
 2015- Pharmacology University of Oxford, Oxford, United Kingdom 
medicinal chemistry, drug discovery, pharmacology
"Barry Potter"
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Shen YC, Arellano-Garcia C, Menjivar RE, et al. (2019) Nonsteroidal sulfamate derivatives as new therapeutic approaches for Neurofibromatosis 2 (NF2). Bmc Pharmacology & Toxicology. 20: 67
Riley AM, Wang H, Shears SB, et al. (2019) Synthesis of an α-phosphono-α,α-difluoroacetamide analogue of the diphosphoinositol pentakisphosphate 5-InsP. Medchemcomm. 10: 1165-1172
Dohle W, Su X, Mills SJ, et al. (2019) A synthetic cyclitol-nucleoside conjugate polyphosphate is a highly potent second messenger mimic. Chemical Science. 10: 5382-5390
Baszczyňski O, Watt JM, Rozewitz MD, et al. (2019) Synthesis of Terminal Ribose Analogues of Adenosine 5'-Diphosphate Ribose as Probes for the Transient Receptor Potential Cation Channel TRPM2. The Journal of Organic Chemistry. 84: 6143-6157
Kühn FJP, Watt JM, Potter BVL, et al. (2019) Different substrate specificities of the two ADPR binding sites in TRPM2 channels of Nematostella vectensis and the role of IDPR. Scientific Reports. 9: 4985
Dohle W, Prota AE, Menchon G, et al. (2019) Tetrahydroisoquinoline Sulfamates as Potent Microtubule Disruptors: Synthesis, Antiproliferative and Antitubulin Activity of Dichlorobenzyl-Based Derivatives, and a Tubulin Cocrystal Structure. Acs Omega. 4: 755-764
Andring J, Dohle W, Tu C, et al. (2019) 3,17β-Bis-sulfamoyloxy-2-methoxyestra-1,3,5(10)-triene (STX140) and Non-Steroidal Sulfamate Derivatives Inhibit Carbonic Anhydrase IX: Structure-Activity Optimization for Isoform Selectivity. Journal of Medicinal Chemistry
Brehm MA, Klemm U, Rehbach C, et al. (2018) Inositol hexakisphosphate increases the size of platelet aggregates. Biochemical Pharmacology
Zhang B, Watt JM, Cordiglieri C, et al. (2018) Small Molecule Antagonists of NAADP-Induced Ca Release in T-Lymphocytes Suggest Potential Therapeutic Agents for Autoimmune Disease. Scientific Reports. 8: 16775
Watt JM, Thomas MP, Potter BVL. (2018) Synthetic cADPR analogues may form only one of two possible conformational diastereoisomers. Scientific Reports. 8: 15268
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