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Page 1
Guanine glycation repair by DJ-1/Park7 and its bacterial homologs.
Richarme G, Liu C, Mihoub M, Abdallah J, Leger T, Joly N, Liebart JC, Jurkunas UV, Nadal M, Bouloc P, Dairou J, Lamouri A. Richarme G, et al. Among authors: lamouri a. Science. 2017 Jul 14;357(6347):208-211. doi: 10.1126/science.aag1095. Epub 2017 Jun 8. Science. 2017. PMID: 28596309
Structure-activity relationships in platelet-activating factor. Part 13: synthesis and biological evaluation of piperazine derivatives with dual anti-PAF and anti-HIV-1 or pure antiretroviral activity.
Serradji N, Bensaid O, Martin M, Sallem W, Dereuddre-Bosquet N, Benmehdi H, Redeuilh C, Lamouri A, Dive G, Clayette P, Heymans F. Serradji N, et al. Among authors: lamouri a. Bioorg Med Chem. 2006 Dec 1;14(23):8109-25. doi: 10.1016/j.bmc.2006.07.031. Epub 2006 Aug 8. Bioorg Med Chem. 2006. PMID: 16893650 Free article.
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: lamouri a. 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
Design of new potent and selective secretory phospholipase A(2) inhibitors. 6-Synthesis, structure-activity relationships and molecular modelling of 1-substituted-4-[4,5-dihydro-1,2,4-(4H)-oxadiazol-5-one-3-yl(methyl)]-functionalized aryl piperazin/one/dione derivatives.
Meddad-Belhabich N, Aoun D, Djimdé A, Redeuilh C, Dive G, Massicot F, Chau F, Heymans F, Lamouri A. Meddad-Belhabich N, et al. Among authors: lamouri a. Bioorg Med Chem. 2010 May 15;18(10):3588-600. doi: 10.1016/j.bmc.2010.03.049. Epub 2010 Mar 27. Bioorg Med Chem. 2010. PMID: 20417107 Free article.
45 results