Logé C - Search Results

1

Design, synthesis, and evaluation of 1-(N-benzylamino)-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents.

Giraud F, Logé C, Pagniez F, Crepin D, Le Pape P, Le Borgne M. Giraud F, et al. Among authors: loge c. Bioorg Med Chem Lett. 2008 Mar 15;18(6):1820-4. doi: 10.1016/j.bmcl.2008.02.027. Epub 2008 Feb 14. Bioorg Med Chem Lett. 2008. PMID: 18313295

2

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. J Enzyme Inhib Med Chem. 2005 Dec;20(6):581-5. doi: 10.1080/14756360500220574. J Enzyme Inhib Med Chem. 2005. PMID: 16408794 Free article.

3

A 3D-QSAR CoMSIA study on 3-azolylmethylindoles as anti-leishmanial agents.

Giraud F, Loge C, Le Borgne M, Pagniez F, Na YM, Le Pape P. Giraud F, et al. Among authors: loge c. SAR QSAR Environ Res. 2006 Jun;17(3):299-309. doi: 10.1080/10659360600787494. SAR QSAR Environ Res. 2006. PMID: 16815769

4

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: loge c. 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

5

Design, synthesis and evaluation of new 6-substituted-5-benzyloxy-4-oxo-4H-pyran-2-carboxamides as potential Src inhibitors.

Farard J, Lanceart G, Logé C, Nourrisson MR, Cruzalegui F, Pfeiffer B, Duflos M. Farard J, et al. Among authors: loge c. J Enzyme Inhib Med Chem. 2008 Oct;23(5):629-40. doi: 10.1080/14756360802205299. J Enzyme Inhib Med Chem. 2008. PMID: 18686137 Free article.

6

Synthesis and structure-activity relationships of 2-phenyl-1-[(pyridinyl- and piperidinylmethyl)amino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents.

Giraud F, Guillon R, Logé C, Pagniez F, Picot C, Le Borgne M, Le Pape P. Giraud F, et al. Among authors: loge c. Bioorg Med Chem Lett. 2009 Jan 15;19(2):301-4. doi: 10.1016/j.bmcl.2008.11.101. Epub 2008 Dec 3. Bioorg Med Chem Lett. 2009. PMID: 19091558

7

Design, synthesis and evaluation of 3-(imidazol- 1-ylmethyl)indoles as antileishmanial agents. Part II.

Giraud F, Loge C, Pagniez F, Crepin D, Barres S, Picot C, Le Pape P, Le Borgne M. Giraud F, et al. Among authors: loge c. J Enzyme Inhib Med Chem. 2009 Oct;24(5):1067-75. doi: 10.1080/14756360802610795. J Enzyme Inhib Med Chem. 2009. PMID: 19555181 Free article.

8

Design of new antifungal agents: synthesis and evaluation of 1-[(1H-indol-5-ylmethyl)amino]-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols.

Guillon R, Giraud F, Logé C, Le Borgne M, Picot C, Pagniez F, Le Pape P. Guillon R, et al. Among authors: loge c. Bioorg Med Chem Lett. 2009 Oct 15;19(20):5833-6. doi: 10.1016/j.bmcl.2009.08.089. Epub 2009 Aug 31. Bioorg Med Chem Lett. 2009. PMID: 19762235

9

Screening for amino acid substitutions in the Candida albicans Erg11 protein of azole-susceptible and azole-resistant clinical isolates: new substitutions and a review of the literature.

Morio F, Loge C, Besse B, Hennequin C, Le Pape P. Morio F, et al. Among authors: loge c. Diagn Microbiol Infect Dis. 2010 Apr;66(4):373-84. doi: 10.1016/j.diagmicrobio.2009.11.006. Diagn Microbiol Infect Dis. 2010. PMID: 20226328 Review.

10

Synthesis and in vitro antifungal evaluation of 2-(2,4-difluorophenyl)-1-[(1H-indol-3-ylmethyl)methylamino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ols.

Guillon R, Logé C, Pagniez F, Ferchaud-Roucher V, Duflos M, Picot C, Le Pape P. Guillon R, et al. Among authors: loge c. J Enzyme Inhib Med Chem. 2011 Apr;26(2):261-9. doi: 10.3109/14756366.2010.503607. Epub 2010 Aug 9. J Enzyme Inhib Med Chem. 2011. PMID: 20695753 Free article.

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