Robert JM - Search Results

1

Thiazolo[5,4-f]quinazolin-9-ones, inhibitors of glycogen synthase kinase-3.

Testard A, Logé C, Léger B, Robert JM, Lozach O, Blairvacq M, Meijer L, Thiéry V, Besson T. Testard A, et al. Among authors: robert jm. Bioorg Med Chem Lett. 2006 Jul 1;16(13):3419-23. doi: 10.1016/j.bmcl.2006.04.006. Epub 2006 Apr 27. Bioorg Med Chem Lett. 2006. PMID: 16644220

2

Novel 9-oxo-thiazolo[5,4-f]quinazoline-2-carbonitrile derivatives as dual cyclin-dependent kinase 1 (CDK1)/glycogen synthase kinase-3 (GSK-3) inhibitors: synthesis, biological evaluation and molecular modeling studies.

Logé C, Testard A, Thiéry V, Lozach O, Blairvacq M, Robert JM, Meijer L, Besson T. Logé C, et al. Among authors: robert jm. Eur J Med Chem. 2008 Jul;43(7):1469-77. doi: 10.1016/j.ejmech.2007.09.020. Epub 2007 Sep 29. Eur J Med Chem. 2008. PMID: 17981370

3

Synthesis of 3,5-bis(2-indolyl)pyridine and 3-[(2-indolyl)-5-phenyl]pyridine derivatives as CDK inhibitors and cytotoxic agents.

Jacquemard U, Dias N, Lansiaux A, Bailly C, Logé C, Robert JM, Lozach O, Meijer L, Mérour JY, Routier S. Jacquemard U, et al. Among authors: robert jm. Bioorg Med Chem. 2008 May 1;16(9):4932-53. doi: 10.1016/j.bmc.2008.03.034. Epub 2008 Mar 17. Bioorg Med Chem. 2008. PMID: 18439832

4

Synthesis of new pyridazino[4,5-b]indol-4-ones and pyridazin-3(2H)-one analogs as DYRK1A inhibitors.

Bruel A, Bénéteau R, Chabanne M, Lozach O, Le Guevel R, Ravache M, Bénédetti H, Meijer L, Logé C, Robert JM. Bruel A, et al. Among authors: robert jm. Bioorg Med Chem Lett. 2014 Nov 1;24(21):5037-40. doi: 10.1016/j.bmcl.2014.09.017. Epub 2014 Sep 16. Bioorg Med Chem Lett. 2014. PMID: 25248682

5

Synthesis and biological evaluation of new 5-benzylated 4-oxo-3,4-dihydro-5H-pyridazino[4,5-b]indoles as PI3Kα inhibitors.

Bruel A, Logé C, Tauzia ML, Ravache M, Le Guevel R, Guillouzo C, Lohier JF, Oliveira Santos JS, Lozach O, Meijer L, Ruchaud S, Bénédetti H, Robert JM. Bruel A, et al. Among authors: robert jm. Eur J Med Chem. 2012 Nov;57:225-33. doi: 10.1016/j.ejmech.2012.09.001. Epub 2012 Sep 10. Eur J Med Chem. 2012. PMID: 23063566

6

Three-dimensional model of cytochrome P450 human aromatase.

Loge C, Le Borgne M, Marchand P, Robert JM, Le Baut G, Palzer M, Hartmann RW. Loge C, et al. Among authors: robert jm. J Enzyme Inhib Med Chem. 2005 Dec;20(6):581-5. doi: 10.1080/14756360500220574. J Enzyme Inhib Med Chem. 2005. PMID: 16408794

7

New selective nonsteroidal aromatase inhibitors: synthesis and inhibitory activity of 2,3 or 5-(alpha-azolylbenzyl)-1H-indoles.

Le Borgne M, Marchand P, Delevoye-Seiller B, Robert JM, Le Baut G, Hartmann RW, Palzer M. Le Borgne M, et al. Among authors: robert jm. Bioorg Med Chem Lett. 1999 Feb 8;9(3):333-6. doi: 10.1016/s0960-894x(98)00737-9. Bioorg Med Chem Lett. 1999. PMID: 10091679

8

Synthesis and immunosuppressive activity evaluation of substituted N-imidazolidin-2-ones and N-tetrahydropyrimidin-2(1H)-ones.

Sabourin C, Robert JM. Sabourin C, et al. Among authors: robert jm. J Enzyme Inhib Med Chem. 2008 Oct;23(5):659-67. doi: 10.1080/14756360802205455. J Enzyme Inhib Med Chem. 2008. PMID: 18821255

9

Inhibition of parasite protein kinase C by new antileishmanial imidazolidin-2-one compounds.

Alvarez N, Robledo S, Velez ID, Robert JM, Le Baut G, Le Pape P. Alvarez N, et al. Among authors: robert jm. J Enzyme Inhib Med Chem. 2002 Dec;17(6):443-7. doi: 10.1080/1475636021000005749. J Enzyme Inhib Med Chem. 2002. PMID: 12683682

10

Cholinesterase inhibition by derivatives of 2-amino-4,6-dimethylpyridine.

Debord J, N'Diaye P, Bollinger JC, Fikri K, Penicaut B, Robert JM, Robert-Piessard S, Le Baut G. Debord J, et al. Among authors: robert jm, robert piessard s. J Enzyme Inhib. 1997 Apr;12(1):13-26. doi: 10.3109/14756369709027660. J Enzyme Inhib. 1997. PMID: 9204379

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