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Results: 1-12 |
Results: 12
Rates of reductive elimination of substituted nitrophenols from the (indol-3-yl)methyl position of indolequinones
Authors: Swann, E Moody, CJ Stratford, MRL Patel, KB Naylor, MA Vojnovic, B Wardman, P Everett, SA
Citation: E. Swann et al., Rates of reductive elimination of substituted nitrophenols from the (indol-3-yl)methyl position of indolequinones, J CHEM S P2, (8), 2001, pp. 1340-1345
Controlling the rates of reductively-activated elimination from the (indol-3-yl)methyl position of indolequinones
Authors: Everett, SA Naylor, MA Barraja, P Swann, E Patel, KB Stratford, MRL Hudnott, AR Vojnovic, B Locke, RJ Wardman, P Moody, CJ
Citation: Sa. Everett et al., Controlling the rates of reductively-activated elimination from the (indol-3-yl)methyl position of indolequinones, J CHEM S P2, (5), 2001, pp. 843-860
Iminoxyl radicals and stable products from the one-electron oxidation of 1-methylindole-3-carbaldehyde oximes
Authors: Everett, SA Naylor, MA Stratford, MRL Patel, KB Ford, E Mortensen, A Ferguson, AC Vojnovic, B Wardman, P
Citation: Sa. Everett et al., Iminoxyl radicals and stable products from the one-electron oxidation of 1-methylindole-3-carbaldehyde oximes, J CHEM S P2, (10), 2001, pp. 1989-1997
1-Methylindole-3-carboxaldehyde oxime derivatives
Authors: Janes, RW Potter, BS Naylor, MA Ferguson, AC Patel, KB Stratford, MRL Wardman, P Everett, SA
Citation: Rw. Janes et al., 1-Methylindole-3-carboxaldehyde oxime derivatives, ACT CRYST C, 57, 2001, pp. 58-61
The relative importance of NADPH: Cytochrome c (P450) reductase for determining the sensitivity of human tumour cells to the indolequinone EO9 and related analogues lacking functionality at the C-2 and C-3 positions
Authors: Saunders, MP Jaffar, M Patterson, AV Nolan, J Naylor, MA Phillips, RM Harris, AL Stratford, IJ
Citation: Mp. Saunders et al., The relative importance of NADPH: Cytochrome c (P450) reductase for determining the sensitivity of human tumour cells to the indolequinone EO9 and related analogues lacking functionality at the C-2 and C-3 positions, BIOCH PHARM, 59(8), 2000, pp. 993-996
Heterocyclic analogues of L-citrulline as inhibitors of the isoforms of nitric oxide synthase (NOS) and identification of N-delta-(4,5-dihydrothiazol-2-yl)ornithine as a potent inhibitor
Authors: Ulhaq, S Chinje, EC Naylor, MA Jaffar, M Stratford, IJ Threadgill, MD
Citation: S. Ulhaq et al., Heterocyclic analogues of L-citrulline as inhibitors of the isoforms of nitric oxide synthase (NOS) and identification of N-delta-(4,5-dihydrothiazol-2-yl)ornithine as a potent inhibitor, BIO MED CH, 7(9), 1999, pp. 1787-1796
Bioreductively-activated prodrugs for targeting hypoxic tissues: Elimination of aspirin from 2-nitroimidazole derivatives
Authors: Everett, SA Naylor, MA Patel, KB Stratford, MRL Wardman, P
Citation: Sa. Everett et al., Bioreductively-activated prodrugs for targeting hypoxic tissues: Elimination of aspirin from 2-nitroimidazole derivatives, BIOORG MED, 9(9), 1999, pp. 1267-1272
Prodrugs for targeting hypoxic tissues: Regiospecific elimination of aspirin from reduced indolequinones
Authors: Jaffar, M Everett, SA Naylor, MA Moore, SG Ulhaq, S Patel, KB Stratford, MRL Nolan, J Wardman, P Stratford, IJ
Citation: M. Jaffar et al., Prodrugs for targeting hypoxic tissues: Regiospecific elimination of aspirin from reduced indolequinones, BIOORG MED, 9(1), 1999, pp. 113-118
Bioreductive activation of a series of indolequinones by human DT-diaphorase: Structure-activity relationships
Authors: Phillips, RM Naylor, MA Jaffar, M Doughty, SW Everett, SA Breen, AG Choudry, GA Stratford, IJ
Citation: Rm. Phillips et al., Bioreductive activation of a series of indolequinones by human DT-diaphorase: Structure-activity relationships, J MED CHEM, 42(20), 1999, pp. 4071-4080
S-2-amino-5-azolylpentanoic acids related to L-ornithine as inhibitors of the isoforms of nitric oxide synthase (NOS)
Authors: Ulhaq, S Chinje, EC Naylor, MA Jaffar, M Stratford, IJ Threadgill, MD
Citation: S. Ulhaq et al., S-2-amino-5-azolylpentanoic acids related to L-ornithine as inhibitors of the isoforms of nitric oxide synthase (NOS), BIO MED CH, 6(11), 1998, pp. 2139-2149
Targeting hypoxia with a new generation of indolequinones
Authors: Jaffar, M Naylor, MA Robertson, N Stratford, IJ
Citation: M. Jaffar et al., Targeting hypoxia with a new generation of indolequinones, ANTI-CAN DR, 13(6), 1998, pp. 593-609
Indolequinone bioreductive drugs: kinetic factors which influence selectivity for hypoxia
Authors: Everett, SA Naylor, MA Nolan, J Patel, KB Wardman, P
Citation: Sa. Everett et al., Indolequinone bioreductive drugs: kinetic factors which influence selectivity for hypoxia, ANTI-CAN DR, 13(6), 1998, pp. 635-653
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