Michaux C - Search Results

1

An unprecedented reversible mode of action of β-lactams for the inhibition of human fatty acid amide hydrolase (hFAAH).

Feledziak M, Michaux C, Lambert DM, Marchand-Brynaert J. Feledziak M, et al. Among authors: michaux c. Eur J Med Chem. 2013 Feb;60:101-11. doi: 10.1016/j.ejmech.2012.11.035. Epub 2012 Nov 29. Eur J Med Chem. 2013. PMID: 23287055

2

A pharmacophore model for sulphonyl-urea (-cyanoguanidine) compounds with dual action, thromboxane receptor antagonists and thromboxane synthase inhibitors.

Michaux C, Dogné JM, Rolin S, Masereel B, Wouters J, Durant F. Michaux C, et al. Eur J Med Chem. 2003 Jul-Aug;38(7-8):703-10. doi: 10.1016/s0223-5234(03)00076-x. Eur J Med Chem. 2003. PMID: 12932901

3

Design, synthesis, and pharmacological evaluation of pyridinic analogues of nimesulide as cyclooxygenase-2 selective inhibitors.

Julémont F, de Leval X, Michaux C, Renard JF, Winum JY, Montero JL, Damas J, Dogné JM, Pirotte B. Julémont F, et al. Among authors: michaux c. J Med Chem. 2004 Dec 30;47(27):6749-59. doi: 10.1021/jm049480l. J Med Chem. 2004. PMID: 15615524

4

A new potential cyclooxygenase-2 inhibitor, pyridinic analogue of nimesulide.

Michaux C, Charlier C, Julémont F, de Leval X, Dogné JM, Pirotte B, Durant F. Michaux C, et al. Eur J Med Chem. 2005 Dec;40(12):1316-24. doi: 10.1016/j.ejmech.2005.08.003. Epub 2005 Oct 11. Eur J Med Chem. 2005. PMID: 16225966

5

Design, synthesis and evaluation of graftable thrombin inhibitors for the preparation of blood-compatible polymer materials.

Salvagnini C, Michaux C, Remiche J, Wouters J, Charlier P, Marchand-Brynaert J. Salvagnini C, et al. Among authors: michaux c. Org Biomol Chem. 2005 Dec 7;3(23):4209-20. doi: 10.1039/b510239a. Epub 2005 Oct 19. Org Biomol Chem. 2005. PMID: 16294249 Free article.

6

Binding mode of new (thio)hydantoin inhibitors of fatty acid amide hydrolase: comparison with two original compounds, OL-92 and JP104.

Michaux C, Muccioli GG, Lambert DM, Wouters J. Michaux C, et al. Bioorg Med Chem Lett. 2006 Sep 15;16(18):4772-6. doi: 10.1016/j.bmcl.2006.06.087. Epub 2006 Jul 17. Bioorg Med Chem Lett. 2006. PMID: 16844375

7

{4(S)-(Piperidin-1-ylcarbonyl)-4-[3-(trifluoromethyl)phenylsulfonamido]butyl}guanidinium chloride: a model of a graftable thrombin inhibitor.

Michaux C, Salvagnini C, Norberg B, Marchand-Brynaert J, Wouters J. Michaux C, et al. Acta Crystallogr C. 2006 Dec;62(Pt 12):o691-3. doi: 10.1107/S0108270106047640. Epub 2006 Nov 22. Acta Crystallogr C. 2006. PMID: 17148914

8

Fatty acid amide hydrolase: from characterization to therapeutics.

Labar G, Michaux C. Labar G, et al. Among authors: michaux c. Chem Biodivers. 2007 Aug;4(8):1882-902. doi: 10.1002/cbdv.200790157. Chem Biodivers. 2007. PMID: 17712824 Review.

9

beta-Lactams derived from a carbapenem chiron are selective inhibitors of human fatty acid amide hydrolase versus human monoacylglycerol lipase.

Feledziak M, Michaux C, Urbach A, Labar G, Muccioli GG, Lambert DM, Marchand-Brynaert J. Feledziak M, et al. Among authors: michaux c. J Med Chem. 2009 Nov 26;52(22):7054-68. doi: 10.1021/jm9008532. J Med Chem. 2009. PMID: 19877691

10

Synthesis, biological evaluation and molecular modeling studies of quinolonyl diketo acid derivatives: new structural insight into the HIV-1 integrase inhibition.

Vandurm P, Guiguen A, Cauvin C, Georges B, Le Van K, Michaux C, Cardona C, Mbemba G, Mouscadet JF, Hevesi L, Van Lint C, Wouters J. Vandurm P, et al. Among authors: michaux c. Eur J Med Chem. 2011 May;46(5):1749-56. doi: 10.1016/j.ejmech.2011.02.028. Epub 2011 Feb 22. Eur J Med Chem. 2011. PMID: 21385662

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