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Synthesis of 6- or 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitors.
Bioorg Med Chem Lett. 2008 Aug 15;18(16):4713-5. doi: 10.1016/j.bmcl.2008.06.094. Epub 2008 Jul 3.
Bioorg Med Chem Lett. 2008.
PMID: 18640836
2- and 3-[(aryl)(azolyl)methyl]indoles as potential non-steroidal aromatase inhibitors.
Lézé MP, Le Borgne M, Marchand P, Loquet D, Kogler M, Le Baut G, Palusczak A, Hartmann RW.
Lézé MP, et al.
J Enzyme Inhib Med Chem. 2004 Dec;19(6):549-57. doi: 10.1080/14756360400004631.
J Enzyme Inhib Med Chem. 2004.
PMID: 15662958
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Synthesis and biological evaluation of 5-[(aryl)(1H-imidazol-1-yl)methyl]-1H-indoles: potent and selective aromatase inhibitors.
Lézé MP, Le Borgne M, Pinson P, Palusczak A, Duflos M, Le Baut G, Hartmann RW.
Lézé MP, et al.
Bioorg Med Chem Lett. 2006 Mar 1;16(5):1134-7. doi: 10.1016/j.bmcl.2005.11.099. Epub 2005 Dec 27.
Bioorg Med Chem Lett. 2006.
PMID: 16380254
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Synthesis, Optimization, Antifungal Activity, Selectivity, and CYP51 Binding of New 2-Aryl-3-azolyl-1-indolyl-propan-2-ols.
Lebouvier N, Pagniez F, Na YM, Shi D, Pinson P, Marchivie M, Guillon J, Hakki T, Bernhardt R, Yee SW, Simons C, Lézé MP, Hartmann RW, Mularoni A, Le Baut G, Krimm I, Abagyan R, Le Pape P, Le Borgne M.
Lebouvier N, et al. Among authors: leze mp.
Pharmaceuticals (Basel). 2020 Aug 8;13(8):186. doi: 10.3390/ph13080186.
Pharmaceuticals (Basel). 2020.
PMID: 32784450
Free PMC article.
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