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T. J. Woodman, P. J. Wood, A. S. Thompson, T. Hutchings, P. Jiao, G. R. Steel, M. D. Threadgill, M. D. Lloyd, "Chiral inversion of NSAID-CoA esters by human alpha-methylacyl-CoA racemase 1A", Chem. Commun., 2011, DOI:10.1039/C1CC10763A;
P. T. Sunderland, E. C. Y. Woon, A. Dhami, A. B. Bergin, M. F. Mahon, P. J. Wood, L. A. Jones, S. R. Tully, M. D. Lloyd, A. S. Thompson, H. Javaid, N. M. B. Martin, M. D. Threadgill, 5-Benzamidoisoquinolin-1-ones and 5-(omega-carboxyalkyl)isoquinolin-1-ones as isoform-selective inhibitors of poly(ADP-ribose)polymerase-2 (PARP-2), 2011, J. Med. Chem. 54, 2049-2059;
S. Pilgrim, G. Kociok-Kohn, M. D. Lloyd, S. E. Lewis, "InosAminoAcids": Novel inositol-amino acid hybrid structures accessed by microbial arene oxidation", 2011, Chem. Commun. 47, 4799-4801;
K. P. Holbourn, M. D. Lloyd, A.S. Thompson, M. D. Threadgill, K. R. Acharya, 'Cloning, purification, crystallisation and preliminary crystallographic analysis of the human histone deacetylase sirtuin 1, 2011, Acta Crys., F67, 461-463;
P. T. Sunderland, A. Dhami, M. F. Mahon, L. A. Jones, S. R. Tully, M. D. Lloyd, A. S. Thompson, H. Javaid, N. B. Martin, M. D. Threadgill, 'Synthesis of 4-alkyl-, 4-aryl-, and arylamino-5-substituted isoquinolin-1-ones and identification of a new PARP-2 selective inhibitor", 2011, Org. Biomol. Chem. 9, 881-891.
F. A. Sattar, D. J. Darley, F. Politano, T. J. Woodman, M. D. Threadgill and M. D. Lloyd, "Unexpected stereoselective exchange of straight-chain fatty acyl-CoA alpha-protons by human alpha-methylacyl-CoA racemase 1A (P504S)", 2010, Chem. Commun., 46, 3348-3350
G. Cozier, M. Leese, M. D. Lloyd, M. Baker, N. Thiayagarajan, K. R. Acharya and B. V. L. Potter, "Structures of human carbonic anhydrase II/inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors" 2010, Biochemistry, 49, 3464-3476
A. Dhami, M. F. Mahon, M. D. Lloyd and M. D. Threadgill, "4-Substituted 5-nitroisoquinolin-1-ones from intramolecular Pd-catalysed reaction of N-(2-alkenyl)-2-halo-3-nitrobenzamides", Tetrahedron, 2009, 65, 4751-4765.
A.-M. Lord, M. Mahon, M. D. Lloyd and M. D. Threadgill, “Design, synthesis and evaluation in vitro of quinoline-8-carboxamides, a new class of poly(adenosine-diphosphate-ribose) polymerase-1 (PARP-1) inhibitor”, J. Med. Chem., 2009, 52, 868-877.
D. J. Darley, D. S. Butler, S. J. Prideaux, T. W. Thornton, A. D. Wilson, T. J. Woodman, M. D. Threadgill and M. D. Lloyd “Synthesis and use of isotope-labelled substrates for a mechanistic study on human α-methylacyl-CoA racemase 1A (AMACR; P504S)”, Org. Biomol. Chem., 2009, 7, 543-552.
A. L. Ball, K. A. Chambers, M. Hewinson, S. Navaratnarajah, L. Samrin, N. Thomas, A. E. H. Tyler, A. J. Wall, M.D. Lloyd, “A microtitre plate assay for measuring glycosidase activity”, J. Enzy. Inhibit. Med. Chem., 2008, 23, 131-135.
M. D. Lloyd, D. J. Darley, A. S. Wierzbicki, M. D. Threadgill “α-Methylacyl-CoA racemase: An ‘obscure’ metabolic enzyme takes centre stage”, FEBS J. 2008, 275, 1089-1102.
M. 6.J. S. W. Kwong, M. F. Mahon, M. D. Lloyd, M. D. Threadgill, “Synthesis of diastereoisomeric homochiral O-protected 4-(arylsulfonimidoyl)butane-1,2,3-triols and conformational and configurational studies”. Tetrahedron, 2007, 12601-12607.
M. D. Lloyd, K. D. E. Boardman, A. Smith, D. M. van den Brink, R. J. A. Wanders, and M. D. Threadgill, “Characterisation of recombinant human aldehyde dehydrogenase 10: Implications for Sj?gren-Larsson syndrome”, J. Enzy. Inhibit. Med. Chem., 2007, 22, 584-590.
T. Searles, D. Butler, W. Chien, M. Mukherji, M. D. Lloyd and C. J. Schofield, “Studies on the specificity of unprocessed and mature forms of phytanoyl-CoA 2-hydroxylase and mutation of iron-binding residues”, J. Lipid Res., 2005, 46, 1660-1666.
K. R. Acharya and M. D. Lloyd, “The advantages and limitations of protein crystal structures”, Trends in Pharmacological Sciences, 2005, 26, 10-14 (review).
M. D. Lloyd, N. Thiyagarajan, Y. T. Ho, L. W. L. Woo, O. B. Sutcliffe, A. Purohit, M. J. Reed, K. R. Acharya, B. V. L. Potter, “First crystal structures of human carbonic anhydrase II in complex with dual aromatase-steroid sulfatase inhibitors”, Biochemistry, 2005, 44, 6858-6866.
M.D. Lloyd, R. L. Pedrick, R. Natesh, L. W. L. Woo, A. Purohit, M. J. Reed, K. R. Acharya and B. V. L. Potter, Crystal structure of human carbonic anhydrase II at 1.95 ? resolution in complex with 667-coumate, a novel anti-cancer agent”, Biochem. J., 2005, 385, 715-720.
M. D. Lloyd, S. J. Lipscomb, K. S. Hewitson, C. M. H. Hensgens,, J. E. Baldwin, C. J. Schofield, “Controlling the substrate selectivity of deacetoxy/deacetylcephalosporin C synthase”, J. Biol. Chem., 2004, 279, 15420-15426.