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  1. η4-Pyrone iron(0)carbonyl complexes as effective CO-releasing molecules (CO-RMs)

    Fairlamb, I. J. S., Duhme-Klair, A., Lynam, J. M., Moulton, B. E., O’Brien, C. T., Whitwood, A. C., Sawle, P., Hammad, J. & Motterlini, R., 2006

    Article in Bioorganic & Medicinal Chemistry Letters

  2. α-L-fucosidase inhibition by pyrrolidine-ferrocene hybrids: Rationalization of ligand-binding properties by structural studies

    Hottin, A., Wright, D. W., Steenackers, A., Delannoy, P., Dubar, F., Biot, C., Davies, G. J. & Behr, J-B., 15 Jul 2013

    Article in Chemistry - A European Journal

  3. rDock: A Fast, Versatile and Open Source Program for Docking Ligands to Proteins and Nucleic Acids

    Ruiz-Carmona, S., Alvarez-Garcia, D., Foloppe, N., Garmendia-Doval, A. B., Juhos, S., Schmidtke, P., Barril, X., Hubbard, R. E. & Morley, S. D., 10 Apr 2014

    Article in PLoS Computational Biology

  4. pBaSysBioll: an integrative plasmid generating gfp transcriptional fusions for high-throughput analysis of gene expression in Bacillus subtilis

    Botella, E., Fogg, M., Jules, M., Piersma, S., Doherty, G., Hansen, A., Denham, E. L., Le Chat, L., Veiga, P., Bailey, K., Lewis, P. J., van Dijl, J. M., Aymerich, S., Wilkinson, A. J. & Devine, K. M., Jun 2010

    Article in Microbiology

  5. p-Di-t-butoxybenzene

    Carman, R. M., Kanizaj, N. & Taylor, R. J. K., 1997

    Article in Australian Journal of Chemistry

  6. fragment-based ligand discovery

    Fischer, M. & Hubbard, R. E., 1 Feb 2009

    Literature review in MOLECULAR INTERVENTIONS

  7. exo-glycal approaches to C-linked glycosyl amino acid synthesis

    Campbell, A. D., Paterson, D. E., Raynham, T. M. & Taylor, R. J. K., 21 Aug 1999

    Article in Chemical Communications

  8. eta(2)(3e)-vinyl complexes and one-electron-transfer reactions: tris(pentafluorophenyl)borane as a one-electron oxidant

    Beddows, C. J., Burrows, A. D., Connelly, N. G., Green, M., Lynam, J. M. & Paget, T. J., 22 Jan 2001

    Article in Organometallics

  9. dUTPase as a platform for antimalarial drug design: Structural basis for the selectivity of a class of nucleoside inhibitors

    Whittingham, J. L., Leal, I., Nguyen, C., Kasinathan, G., Bell, E., Jones, A. F., Berry, C., Benito, A., Turkenburg, J. P., Dodson, E. J., Perez, L. M. R., Wilkinson, T., Johansson, N. G., Brun, R., Gilbert, I. H., Pacanowska, D. G. & Wilson, K. S., 8 Feb 2005

    Article in Structure

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