Muccioli GG - Search Results

1

3-Alkenyl-2-azetidinones as fatty acid amide hydrolase inhibitors.

Urbach A, Muccioli GG, Stern E, Lambert DM, Marchand-Brynaert J. Urbach A, et al. Among authors: muccioli gg. Bioorg Med Chem Lett. 2008 Jul 15;18(14):4163-7. doi: 10.1016/j.bmcl.2008.05.081. Epub 2008 May 24. Bioorg Med Chem Lett. 2008. PMID: 18547805

2

Versatile access to benzhydryl-phenylureas through an unexpected rearrangement during microwave-enhanced synthesis of hydantoins.

Muccioli GG, Wouters J, Poupaert JH, Norberg B, Poppitz W, Scriba GK, Lambert DM. Muccioli GG, et al. Org Lett. 2003 Oct 2;5(20):3599-602. doi: 10.1021/ol035282x. Org Lett. 2003. PMID: 14507182

3

Characterization of the pharmacology of imidazolidinedione derivatives at cannabinoid CB1 and CB2 receptors.

Govaerts SJ, Muccioli GG, Hermans E, Lambert DM. Govaerts SJ, et al. Among authors: muccioli gg. Eur J Pharmacol. 2004 Jul 8;495(1):43-53. doi: 10.1016/j.ejphar.2004.05.023. Eur J Pharmacol. 2004. PMID: 15219819

4

Substituted 5,5'-diphenyl-2-thioxoimidazolidin-4-one as CB1 cannabinoid receptor ligands: synthesis and pharmacological evaluation.

Muccioli GG, Martin D, Scriba GK, Poppitz W, Poupaert JH, Wouters J, Lambert DM. Muccioli GG, et al. J Med Chem. 2005 Apr 7;48(7):2509-17. doi: 10.1021/jm049263k. J Med Chem. 2005. PMID: 15801840

5

Current knowledge on the antagonists and inverse agonists of cannabinoid receptors.

Muccioli GG, Lambert DM. Muccioli GG, et al. Curr Med Chem. 2005;12(12):1361-94. doi: 10.2174/0929867054020891. Curr Med Chem. 2005. PMID: 15974990 Review.

6

1-Benzhydryl-3-phenylurea and 1-benzhydryl-3-phenylthiourea derivatives: new templates among the CB1 cannabinoid receptor inverse agonists.

Muccioli GG, Wouters J, Scriba GK, Poppitz W, Poupaert JH, Lambert DM. Muccioli GG, et al. J Med Chem. 2005 Nov 17;48(23):7486-90. doi: 10.1021/jm0503906. J Med Chem. 2005. PMID: 16279809

7

Novel 4-oxo-1,4-dihydroquinoline-3-carboxamide derivatives as new CB2 cannabinoid receptors agonists: synthesis, pharmacological properties and molecular modeling.

Stern E, Muccioli GG, Millet R, Goossens JF, Farce A, Chavatte P, Poupaert JH, Lambert DM, Depreux P, Hénichart JP. Stern E, et al. Among authors: muccioli gg. J Med Chem. 2006 Jan 12;49(1):70-9. doi: 10.1021/jm050467q. J Med Chem. 2006. PMID: 16392793

8

Substituted 2-thioxoimidazolidin-4-ones and imidazolidine-2,4-diones as fatty acid amide hydrolase inhibitors templates.

Muccioli GG, Fazio N, Scriba GK, Poppitz W, Cannata F, Poupaert JH, Wouters J, Lambert DM. Muccioli GG, et al. J Med Chem. 2006 Jan 12;49(1):417-25. doi: 10.1021/jm050977k. J Med Chem. 2006. PMID: 16392827

9

Synthesis and activity of 1,3,5-triphenylimidazolidine-2,4-diones and 1,3,5-triphenyl-2-thioxoimidazolidin-4-ones: characterization of new CB1 cannabinoid receptor inverse agonists/antagonists.

Muccioli GG, Wouters J, Charlier C, Scriba GK, Pizza T, Di Pace P, De Martino P, Poppitz W, Poupaert JH, Lambert DM. Muccioli GG, et al. J Med Chem. 2006 Feb 9;49(3):872-82. doi: 10.1021/jm050484f. J Med Chem. 2006. PMID: 16451053

10

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. Among authors: muccioli gg. 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

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