Publications

  • Journals

    Asad, N.; McLain, D. E.; Condon, A. F.; Gore. S.; Hampton, S. E.; Vijay, S.; Williams, J. T.; Dore. T. M. Photoactivatable Dopamine and Sulpiride to Explore the Function of Dopaminergic Neurons and Circuits. ACS Chem. Neurosci. Accepted.

    Pérez-Moreno, G.; Sánchez-Carrasco, P.; Ruiz-Pérez, L. M.; Johansson, N. G.; Müller, S.; Baragaña, B.; Hampton, S. E.; Gilbert, I. H.; Kaiser, M.; Sarkar, S.; Pandurangan, T.; Kumar, V.; González-Pacanowska, D. Validation of Plasmodium falciparum dUTPase as the target of 5'-tritylated deoxyuridine analogues with anti-malarial activity. Malar. J. 2019, 18, 392.

    Hampton, S. E.; Dore, T. M.; Schmidt , W. K. Rce1: Mechanism and Inhibitors. Crit. Rev. Biochem. Mol. Biol. 201853, 157-174.

    Mohammed, I.; Hampton, S. E.; Ashall, L.; Hildebrandt, E. R.; Kutlik, R. A.; Manandhar, S. P.; Floyd, B. J.; Smith, H. E.; Dozier, J. K.; Distefano, M. D.; Schmidt, W. K.; Dore, T. M. 8-Hydroxyquinoline-Based Inhibitors of the Rce1 Protease Disrupt Ras Membrane Localization in Human Cells. Bioorg. Med. Chem. 2016, 24, 160-178

    Hampton, S. E.; Schipani, A.; Bosch-Navarrete, C.; Recio, E.; Kaiser, M.; Kahnberg, P.; Gonzalez-Pacanowska, D.; Johansson, N. G.; Gilbert, I. H. Investigation of Acyclic Uridine Amide and 5'-Amido Nucleoside Analogues as Potential Inhibitors of the Plasmodium falciparum dUTPase. Bioorg. Med. Chem. 2013, 21, 5876-5885.

    Hampton, S. E.; Baragana, B.; Schipani, A.; Bosch-Navarrete, C.; Musso-Buendia, J. A.; Recio, E.; Kaiser, M.; Whittingham, J. L.; Roberts, S. M.; Shevtsov, M.; Brannigan, J. A.; Kahnberg, P.; Brun, R.; Wilson, K. S.; Gonzalez-Pacanowska, D.; Johansson, N. G.; Gilbert, I. H. Design, Synthesis, and Evaluation of 5'-Diphenyl Nucleoside Analogues as Inhibitors of the Plasmodium falciparum dUTPase. ChemMedChem 2011, 6, 1816-1831.