School of Pharmacy

Publications in the Biomolecular Science and Medicinal Chemistry Division

Publications

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ABUKHADER, M., HEAP, J., DE MATTEIS, C., KELLAM, B., DOUGHTY, S.W., MINTON, N. and PAOLI, M., 2005. Binding of the anticancer prodrug CB1954 to the activating enzyme NQ02 revealed by the crystal structure of their complex Journal of Medicinal Chemistry. 48(24), 7714-7719

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DE BANK, P. A., KELLAM, B., KENDALL, D. A. and SHAKESHEFF, K. M., 2005. Altered cellular response to adsorbed matrix protein by chemoselective ligation of small molecules JOURNAL OF MATERIALS CHEMISTRY. VOL 15, 2047-2055

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KELLAM,B., WARD,PA.., RAHIM,A.S.A. and CHHABRA,S.R., 2005. Nα-Dmc protected amino acid aglycones: versatile hydrogenolysis stable acceptors for O-glycosylation Tetrahedron Letters. 46(10), 1703-1706

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SEDMAN, V.L., ALLEN, S., CHAN, W.C., KELLAM, B. and TENDLER S.J.B., 2005. Functionalizing human amylin (20-29) fibrils FEBS Journal. 272, 517-518

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ALI, BE, DE BANK, PA, KELLAM, B and SHAKESHEFF, KM, 2005. Controlled cell aggregation via cell-surface engineering International Journal of Experimental Pathology. 86(3), A21-A22

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SEDMAN, V.L., ALLEN, S., CHAN, W.C., DAVIES, M.C., ROBERTS, C.J., TENDLER, S.J.B. and WILLIAMS, P.M., 2005. Atomic force microscopy study of human amylin (20-29) fibrils Protein and Peptide Letters. 12(1), 79-83

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GARDINER, L., COYLE, B.J, CHAN, W.C and SOULTANAS, P., 2005. Discovery of antagonist peptides against bacterial helicase-primase interaction in B. stearothermophilus by reverse yeast three-hybrid. Chemistry & Biology. 12(5), 595-604

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SEDMAN, V.L., ALLEN, S., CHAN, W.C., KELLAM, B. and TENDLER S.J.B., 2005. Functionalizing human amylin (20-29) fibrils FEBS Journal. 272, 517-518

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SEVILLE, LUCY L, SHAH, NITA, WESTWELL, ANDREW D and CHAN, WENG C, 2005. Modulation of pRB/E2F functions in the regulation of cell cycle and in cancer. Current Cancer Drug Targets. 5(3), 159-70

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ZHELEVA, D.L., FISCHER, P.M., MCINNES, C., ANDREWS, M.J.I., CHAN, W.C. and ATKINSON, G.E., 2005. Cyclin binding peptides, and their use in drug screening assays WO 2005/040802 A3 05/06/2005 00:00:00

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BOURQUE, E, KOCIENSKI, PJ, STOCKS, M and YUEN, J, 2005. Synthesis of the c14-c28 fragment of tetronasin Synthesis-Stuttgart. 3219-3224

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STOCKS, MJ, BARBER, S, FORD, R, LEROUX, F, ST-GALLAY, S, TEAGUE, S and XUE, YF, 2005. Structure-driven htl: Design and synthesis of novel aminoindazole inhibitors of c-jun n-terminal kinase activity Bioorganic & Medicinal Chemistry Letters. 15(14), 3459-3462

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MUKHERJEE, A., WESTWELL, A.D., BRADSHAW, T.D., STEVENS, M.F.G., CARMICHAEL, J. and MARTIN, S.G., 2005. Cytotoxic and antiangiogenic activity of AW464 (NSC 706704), a novel thioredoxin inhibitor: an in vitro study British Journal of Cancer. 92, 350-358

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BERRY, J.M., BRADSHAW, T.D., FICHTNER, I., REN, R., SCHWALBE, C.H., WELLS, G., CHEW, E.-H., STEVENS, M.F.G. and WESTWELL, A.D., 2005. Quinols as novel therapeutic agents. 2. 4-(1-arylsulfonylindol-2-yl)-4-hydroxycyclohexa-2,5-dien-1-ones and related agents as potent and selective antitumor agents Journal of Medicinal Chemistry. 48(2), 639-644

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BRADSHAW,T.D., MORTIMER,C.G. and WESTWELL,A.D., 2005. Update to: the aryl hydrocarbon receptor in anticancer drug discovery: friend or foe? Medicinal Chemistry Reviews - Online. 2(2), 153-161
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