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Results: 1-14 |
Results: 14
A novel mechanism of antibiotic resistance: study of the complex state of peptides with bacterial Staphylococcus aureus ribosomes
Authors: Verdier, L Gharbi-Benarous, J Bertho, G Mauvais, P Girault, JP
Citation: L. Verdier et al., A novel mechanism of antibiotic resistance: study of the complex state of peptides with bacterial Staphylococcus aureus ribosomes, CR AC S IIC, 4(10), 2001, pp. 745-750
Synthesis of analogues of the O-beta-D-ribofuranosyl nucleoside moiety of liposidomycins. part 2: Role of the hydroxyl groups upon the inhibition of MraY
Authors: Dini, C Drochon, N Guillot, JC Mauvais, P Walter, P Aszodi, J
Citation: C. Dini et al., Synthesis of analogues of the O-beta-D-ribofuranosyl nucleoside moiety of liposidomycins. part 2: Role of the hydroxyl groups upon the inhibition of MraY, BIOORG MED, 11(4), 2001, pp. 533-536
Fine tuning of physico-chemical parameters to optimise a new series of novobiocin analogues
Authors: Schio, L Chatreaux, F Loyau, V Murer, M Ferreira, A Mauvais, P Bonnefoy, A Klich, M
Citation: L. Schio et al., Fine tuning of physico-chemical parameters to optimise a new series of novobiocin analogues, BIOORG MED, 11(11), 2001, pp. 1461-1464
Dissociation-equilibrium constant and bound conformation for weak antibiotic binding interaction with different bacterial ribosomes
Authors: Verdier, L Gharbi-Benarous, J Bertho, G Evrard-Todeschi, N Mauvais, P Girault, JP
Citation: L. Verdier et al., Dissociation-equilibrium constant and bound conformation for weak antibiotic binding interaction with different bacterial ribosomes, J CHEM S P2, (12), 2000, pp. 2363-2371
Coumarin inhibitors of gyrase B with N-propargyloxy-carbamate as an effective pyrrole bioisostere
Authors: Periers, AM Laurin, P Ferroud, D Haesslein, JL Klich, M Dupuis-Hamelin, C Mauvais, P Lassaigne, P Bonnefoy, A Musicki, B
Citation: Am. Periers et al., Coumarin inhibitors of gyrase B with N-propargyloxy-carbamate as an effective pyrrole bioisostere, BIOORG MED, 10(2), 2000, pp. 161-165
Synthesis of the nucleoside moiety of liposidomycins: Elucidation of the pharmacophore of this family of MraY inhibitors
Authors: Dini, C Collette, P Drochon, N Guillot, JC Lemoine, G Mauvais, P Aszodi, J
Citation: C. Dini et al., Synthesis of the nucleoside moiety of liposidomycins: Elucidation of the pharmacophore of this family of MraY inhibitors, BIOORG MED, 10(16), 2000, pp. 1839-1843
Macrolide-ketolide inhibition of MLS-resistant ribosomes is improved by alternative drug interaction with domain II of 23S rRNA
Authors: Douthwaite, S Hansen, LH Mauvais, P
Citation: S. Douthwaite et al., Macrolide-ketolide inhibition of MLS-resistant ribosomes is improved by alternative drug interaction with domain II of 23S rRNA, MOL MICROB, 36(1), 2000, pp. 183-192
Synthesis of isothiochroman 2,2-dioxide and 1,2-benzooxathiin 2,2-dioxide gyrase B inhibitors
Authors: Peixoto, C Laurin, P Klich, M Dupuis-Hamelin, C Mauvais, P Lassaigne, P Bonnefoy, A Musicki, B
Citation: C. Peixoto et al., Synthesis of isothiochroman 2,2-dioxide and 1,2-benzooxathiin 2,2-dioxide gyrase B inhibitors, TETRAHEDR L, 41(11), 2000, pp. 1741-1745
Measurement of the dissociation-equilibrium constants for low affinity antibiotic binding interaction with bacterial ribosomes by the T-2 (CPMG) and line-broadening methods
Authors: Verdier, L Gharbi-Benarous, J Bertho, G Mauvais, P Giraud, JP
Citation: L. Verdier et al., Measurement of the dissociation-equilibrium constants for low affinity antibiotic binding interaction with bacterial ribosomes by the T-2 (CPMG) and line-broadening methods, J CHIM PHYS, 96(9-10), 1999, pp. 1616-1623
Structure-activity relationship in two series of aminoalkyl substituted coumarin inhibitors of gyrase B
Authors: Laurin, P Ferroud, D Schio, L Klich, M Dupuis-Hamelin, C Mauvais, P Lassaigne, P Bonnefoy, A Musicki, B
Citation: P. Laurin et al., Structure-activity relationship in two series of aminoalkyl substituted coumarin inhibitors of gyrase B, BIOORG MED, 9(19), 1999, pp. 2875-2880
Synthesis and biological evaluation of coumarincarboxylic acids as inhibitors of gyrase B. L-rhamnose as an effective substitute for L-noviose
Authors: Ferroud, D Collard, J Klich, M Dupuis-Hamelin, C Mauvais, P Lassaigne, P Bonnefoy, A Musicki, B
Citation: D. Ferroud et al., Synthesis and biological evaluation of coumarincarboxylic acids as inhibitors of gyrase B. L-rhamnose as an effective substitute for L-noviose, BIOORG MED, 9(19), 1999, pp. 2881-2886
Synthesis and in vitro evaluation of novel highly potent coumarin inhibitors of gyrase B
Authors: Laurin, P Ferroud, D Klich, M Dupuis-Hamelin, C Mauvais, P Lassaigne, P Bonnefoy, A Musicki, B
Citation: P. Laurin et al., Synthesis and in vitro evaluation of novel highly potent coumarin inhibitors of gyrase B, BIOORG MED, 9(14), 1999, pp. 2079-2084
The macrolide-ketolide antibiotic binding site is formed by structures in domains II and V of 23S ribosomal RNA
Authors: Hansen, LH Mauvais, P Douthwaite, S
Citation: Lh. Hansen et al., The macrolide-ketolide antibiotic binding site is formed by structures in domains II and V of 23S ribosomal RNA, MOL MICROB, 31(2), 1999, pp. 623-631
A ketolide resistance mutation in domain II of 23S rRNA reveals the proximity of hairpin 35 to the peptidyl transferase centre
Authors: Xiong, LQ Shah, S Mauvais, P Mankin, AS
Citation: Lq. Xiong et al., A ketolide resistance mutation in domain II of 23S rRNA reveals the proximity of hairpin 35 to the peptidyl transferase centre, MOL MICROB, 31(2), 1999, pp. 633-639
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