Salmon L - Search Results

1

Bisphosphonate Inhibitors of Mammalian Glycolytic Aldolase.

Heron PW, Abellán-Flos M, Salmon L, Sygusch J. Heron PW, et al. Among authors: salmon l. J Med Chem. 2018 Dec 13;61(23):10558-10572. doi: 10.1021/acs.jmedchem.8b01000. Epub 2018 Dec 3. J Med Chem. 2018. PMID: 30418024

2

Synthesis and evaluation of a new inhibitor of phosphoglucose isomerases: the enediolate analogue 5-phospho-D-arabinohydroxamate.

Hardré R, Bonnette C, Salmon L, Gaudemer A. Hardré R, et al. Among authors: salmon l. Bioorg Med Chem Lett. 1998 Dec 1;8(23):3435-8. doi: 10.1016/s0960-894x(98)00621-0. Bioorg Med Chem Lett. 1998. PMID: 9873748

3

Preliminary studies on the inhibition of D-sorbitol-6-phosphate 2-dehydrogenase from Escherichia coli with substrate analogues.

Roux C, Salmon L, Verchère-Béaur C. Roux C, et al. Among authors: salmon l. J Enzyme Inhib Med Chem. 2006 Apr;21(2):187-92. doi: 10.1080/14756360500535260. J Enzyme Inhib Med Chem. 2006. PMID: 16791965 Free article.

4

Synthesis and evaluation of non-hydrolyzable D-mannose 6-phosphate surrogates reveal 6-deoxy-6-dicarboxymethyl-D-mannose as a new strong inhibitor of phosphomannose isomerases.

Foret J, de Courcy B, Gresh N, Piquemal JP, Salmon L. Foret J, et al. Among authors: salmon l. Bioorg Med Chem. 2009 Oct 15;17(20):7100-7. doi: 10.1016/j.bmc.2009.09.005. Epub 2009 Sep 6. Bioorg Med Chem. 2009. PMID: 19783448

5

Synthesis and evaluation of malonate-based inhibitors of phosphosugar-metabolizing enzymes: class II fructose-1,6-bis-phosphate aldolases, type I phosphomannose isomerase, and phosphoglucose isomerase.

Desvergnes S, Courtiol-Legourd S, Daher R, Dabrowski M, Salmon L, Therisod M. Desvergnes S, et al. Among authors: salmon l. Bioorg Med Chem. 2012 Feb 15;20(4):1511-20. doi: 10.1016/j.bmc.2011.12.050. Epub 2012 Jan 2. Bioorg Med Chem. 2012. PMID: 22269276

6

Structural basis for competitive inhibition of 3,4-dihydroxy-2-butanone-4-phosphate synthase from Vibrio cholerae.

Islam Z, Kumar A, Singh S, Salmon L, Karthikeyan S. Islam Z, et al. Among authors: salmon l. J Biol Chem. 2015 May 1;290(18):11293-308. doi: 10.1074/jbc.M114.611830. Epub 2015 Mar 18. J Biol Chem. 2015. PMID: 25792735 Free PMC article.

7

Novel N-substituted 5-phosphate-d-arabinonamide derivatives as strong inhibitors of phosphoglucose isomerases: Synthesis, structure-activity relationship and crystallographic studies.

Ahmad L, Plancqueel S, Lazar N, Korri-Youssoufi H, Li de la Sierra-Gallay I, van Tilbeurgh H, Salmon L. Ahmad L, et al. Among authors: salmon l. Bioorg Chem. 2020 Sep;102:104048. doi: 10.1016/j.bioorg.2020.104048. Epub 2020 Jun 29. Bioorg Chem. 2020. PMID: 32682158

8

Synthesis and kinetic evaluation of phosphomimetic inhibitors targeting type B ribose-5-phosphate isomerase from Mycobacterium tuberculosis.

Courtiol-Legourd S, Mariano S, Foret J, Roos AK, Mowbray SL, Salmon L. Courtiol-Legourd S, et al. Among authors: salmon l. Bioorg Med Chem Lett. 2024 Apr 1;102:129666. doi: 10.1016/j.bmcl.2024.129666. Epub 2024 Feb 19. Bioorg Med Chem Lett. 2024. PMID: 38382679

9

Binding of 5-phospho-D-arabinonohydroxamate and 5-phospho-D-arabinonate inhibitors to zinc phosphomannose isomerase from Candida albicans studied by polarizable molecular mechanics and quantum mechanics.

Roux C, Gresh N, Perera LE, Piquemal JP, Salmon L. Roux C, et al. Among authors: salmon l. J Comput Chem. 2007 Apr 15;28(5):938-57. doi: 10.1002/jcc.20586. J Comput Chem. 2007. PMID: 17253648

10

Complexes of a Zn-metalloenzyme binding site with hydroxamate-containing ligands. A case for detailed benchmarkings of polarizable molecular mechanics/dynamics potentials when the experimental binding structure is unknown.

Gresh N, Perahia D, de Courcy B, Foret J, Roux C, El-Khoury L, Piquemal JP, Salmon L. Gresh N, et al. Among authors: salmon l. J Comput Chem. 2016 Dec 15;37(32):2770-2782. doi: 10.1002/jcc.24503. Epub 2016 Oct 4. J Comput Chem. 2016. PMID: 27699809

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