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Inhibition of secretory phospholipase A2. 2-Synthesis and structure-activity relationship studies of 4,5-dihydro-3-(4-tetradecyloxybenzyl)-1,2,4-4H-oxadiazol-5-one (PMS1062) derivatives specific for group II enzyme.
Dong CZ, Ahamada-Himidi A, Plocki S, Aoun D, Touaibia M, Meddad-Bel Habich N, Huet J, Redeuilh C, Ombetta JE, Godfroid JJ, Massicot F, Heymans F. Dong CZ, et al. Among authors: touaibia m. Bioorg Med Chem. 2005 Mar 15;13(6):1989-2007. doi: 10.1016/j.bmc.2005.01.016. Bioorg Med Chem. 2005. PMID: 15727853
Design of new potent and selective secretory phospholipase A2 inhibitors. Part 5: synthesis and biological activity of 1-alkyl-4-[4,5-dihydro-1,2,4-[4H]-oxadiazol-5-one-3-ylmethylbenz-4'-yl(oyl)] piperazines.
Boukli L, Touaibia M, Meddad-Belhabich N, Djimdé A, Park CH, Kim JJ, Yoon JH, Lamouri A, Heymans F. Boukli L, et al. Among authors: touaibia m. Bioorg Med Chem. 2008 Feb 1;16(3):1242-53. doi: 10.1016/j.bmc.2007.10.077. Epub 2007 Nov 13. Bioorg Med Chem. 2008. PMID: 17993277
Caffeic Acid, a versatile pharmacophore: an overview.
Touaibia M, Jean-François J, Doiron J. Touaibia M, et al. Mini Rev Med Chem. 2011 Jul;11(8):695-713. doi: 10.2174/138955711796268750. Mini Rev Med Chem. 2011. PMID: 21679136 Review.
78 results