Mauvais P - Search Results

1

Nonclinical and human pharmacology of the potent and selective topical retinoic acid receptor-γ agonist trifarotene.

Aubert J, Piwnica D, Bertino B, Blanchet-Réthoré S, Carlavan I, Déret S, Dreno B, Gamboa B, Jomard A, Luzy AP, Mauvais P, Mounier C, Pascau J, Pelisson I, Portal T, Rivier M, Rossio P, Thoreau E, Vial E, Voegel JJ. Aubert J, et al. Among authors: mauvais p. Br J Dermatol. 2018 Aug;179(2):442-456. doi: 10.1111/bjd.16719. Epub 2018 Jul 4. Br J Dermatol. 2018. PMID: 29974453 Clinical Trial.

2

Highly potent naphthofuran-based retinoic acid receptor agonists.

Santín EP, Khanwalkar H, Voegel J, Collette P, Mauvais P, Gronemeyer H, de Lera AR. Santín EP, et al. Among authors: mauvais p. ChemMedChem. 2009 May;4(5):780-91. doi: 10.1002/cmdc.200900015. ChemMedChem. 2009. PMID: 19350615

3

Pyrazine arotinoids with inverse agonist activities on the retinoid and rexinoid receptors.

García J, Khanwalkar H, Pereira R, Erb C, Voegel JJ, Collette P, Mauvais P, Bourguet W, Gronemeyer H, de Lera AR. García J, et al. Among authors: mauvais p. Chembiochem. 2009 May 4;10(7):1252-9. doi: 10.1002/cbic.200900030. Chembiochem. 2009. PMID: 19343742

4

Design and synthesis of bridged gamma-lactams as analogues of beta-lactam antibiotics.

Aszodi J, Rowlands DA, Mauvais P, Collette P, Bonnefoy A, Lampilas M. Aszodi J, et al. Among authors: mauvais p. Bioorg Med Chem Lett. 2004 May 17;14(10):2489-92. doi: 10.1016/j.bmcl.2004.03.004. Bioorg Med Chem Lett. 2004. PMID: 15109638

5

Synthesis of the nucleoside moiety of liposidomycins: elucidation of the pharmacophore of this family of MraY inhibitors.

Dini C, Collette P, Drochon N, Guillot JC, Lemoine G, Mauvais P, Aszodi J. Dini C, et al. Among authors: mauvais p. Bioorg Med Chem Lett. 2000 Aug 21;10(16):1839-43. doi: 10.1016/s0960-894x(00)00349-8. Bioorg Med Chem Lett. 2000. PMID: 10969981

6

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.

Dini C, Drochon N, Guillot JC, Mauvais P, Walter P, Aszodi J. Dini C, et al. Among authors: mauvais p. Bioorg Med Chem Lett. 2001 Feb 26;11(4):533-6. doi: 10.1016/s0960-894x(00)00714-9. Bioorg Med Chem Lett. 2001. PMID: 11229764

7

Fine Tuning of physico-chemical parameters to optimise a new series of novobiocin analogues.

Schio L, Chatreaux F, Loyau V, Murer M, Ferreira A, Mauvais P, Bonnefoy A, Klich M. Schio L, et al. Among authors: mauvais p. Bioorg Med Chem Lett. 2001 Jun 4;11(11):1461-4. doi: 10.1016/s0960-894x(01)00257-8. Bioorg Med Chem Lett. 2001. PMID: 11378377

8

Synthesis and in vitro evaluation of novel highly potent coumarin inhibitors of gyrase B.

Laurin P, Ferroud D, Klich M, Dupuis-Hamelin C, Mauvais P, Lassaigne P, Bonnefoy A, Musicki B. Laurin P, et al. Among authors: mauvais p. Bioorg Med Chem Lett. 1999 Jul 19;9(14):2079-84. doi: 10.1016/s0960-894x(99)00329-7. Bioorg Med Chem Lett. 1999. PMID: 10450985

9

Structure-activity relationship in two series of aminoalkyl substituted coumarin inhibitors of gyrase B.

Laurin P, Ferroud D, Schio L, Klich M, Dupuis-Hamelin C, Mauvais P, Lassaigne P, Bonnefoy A, Musicki B. Laurin P, et al. Among authors: mauvais p. Bioorg Med Chem Lett. 1999 Oct 4;9(19):2875-80. doi: 10.1016/s0960-894x(99)00492-8. Bioorg Med Chem Lett. 1999. PMID: 10522710

10

Synthesis and biological evaluation of coumarincarboxylic acids as inhibitors of gyrase B. L-rhamnose as an effective substitute for L-noviose.

Ferroud D, Collard J, Klich M, Dupuis-Hamelin C, Mauvais P, Lassaigne P, Bonnefoy A, Musicki B. Ferroud D, et al. Among authors: mauvais p. Bioorg Med Chem Lett. 1999 Oct 4;9(19):2881-6. doi: 10.1016/s0960-894x(99)00493-x. Bioorg Med Chem Lett. 1999. PMID: 10522711

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