Tarnus C - Search Results

1

Asymmetric synthesis of the L-fuco-nojirimycin, a nanomolar alpha-L-fucosidase inhibitor.

Dubernet M, Defoin A, Tarnus C. Dubernet M, et al. Among authors: tarnus c. Bioorg Med Chem Lett. 2006 Mar 1;16(5):1172-4. doi: 10.1016/j.bmcl.2005.11.100. Epub 2005 Dec 20. Bioorg Med Chem Lett. 2006. PMID: 16376079

2

Synthesis and structure activity relationships of novel non-peptidic metallo-aminopeptidase inhibitors.

Albrecht S, Defoin A, Salomon E, Tarnus C, Wetterholm A, Haeggström JZ. Albrecht S, et al. Among authors: tarnus c. Bioorg Med Chem. 2006 Nov 1;14(21):7241-57. doi: 10.1016/j.bmc.2006.06.050. Epub 2006 Jul 17. Bioorg Med Chem. 2006. PMID: 16844380

3

Synthesis and evaluation of amino-threoses in D- and L-series: are five membered ring amino-sugars more potent glycosidase inhibitors than the six membered ones?

Chevrier C, Defoin A, Tarnus C. Chevrier C, et al. Among authors: tarnus c. Bioorg Med Chem. 2007 Jun 15;15(12):4125-35. doi: 10.1016/j.bmc.2007.03.073. Epub 2007 Mar 30. Bioorg Med Chem. 2007. PMID: 17434740

4

Synthesis of all-cis 2,5-imino-2,5-dideoxy-fucitol and its evaluation as a potent fucosidase and galactosidase inhibitor.

Ak A, Prudent S, LeNouën D, Defoin A, Tarnus C. Ak A, et al. Among authors: tarnus c. Bioorg Med Chem Lett. 2010 Dec 15;20(24):7410-3. doi: 10.1016/j.bmcl.2010.10.043. Epub 2010 Oct 15. Bioorg Med Chem Lett. 2010. PMID: 21050758

5

Amino-benzosuberone: a novel warhead for selective inhibition of human aminopeptidase-N/CD13.

Albrecht S, Al-Lakkis-Wehbe M, Orsini A, Defoin A, Pale P, Salomon E, Tarnus C, Weibel JM. Albrecht S, et al. Among authors: tarnus c. Bioorg Med Chem. 2011 Feb 15;19(4):1434-49. doi: 10.1016/j.bmc.2011.01.008. Epub 2011 Jan 11. Bioorg Med Chem. 2011. PMID: 21292493

6

Synthesis of 4-amino-4,5-dideoxy-L-lyxofuranose derivatives and their evaluation as fucosidase inhibitors.

Chevrier C, Le Nouën D, Defoin A, Tarnus C. Chevrier C, et al. Among authors: tarnus c. Carbohydr Res. 2011 Jul 15;346(10):1202-11. doi: 10.1016/j.carres.2011.03.030. Epub 2011 Mar 24. Carbohydr Res. 2011. PMID: 21550024

7

A novel amino-benzosuberone derivative is a picomolar inhibitor of mammalian aminopeptidase N/CD13.

Maiereanu C, Schmitt C, Schifano-Faux N, Le Nouën D, Defoin A, Tarnus C. Maiereanu C, et al. Among authors: tarnus c. Bioorg Med Chem. 2011 Sep 15;19(18):5716-33. doi: 10.1016/j.bmc.2011.06.089. Epub 2011 Jul 19. Bioorg Med Chem. 2011. PMID: 21843945

8

Rapid and efficient synthesis of a novel series of substituted aminobenzosuberone derivatives as potent, selective, non-peptidic neutral aminopeptidase inhibitors.

Albrecht S, Salomon E, Defoin A, Tarnus C. Albrecht S, et al. Among authors: tarnus c. Bioorg Med Chem. 2012 Aug 15;20(16):4942-53. doi: 10.1016/j.bmc.2012.06.041. Epub 2012 Jun 28. Bioorg Med Chem. 2012. PMID: 22796349

9

Synthesis of amino-hydroxy-benzocycloheptenones as potent, selective, non-peptidic dinuclear zinc metalloaminopeptidase inhibitors.

Al-Lakkis-Wehbe M, Chaillou B, Defoin A, Albrecht S, Tarnus C. Al-Lakkis-Wehbe M, et al. Among authors: tarnus c. Bioorg Med Chem. 2013 Nov 1;21(21):6447-55. doi: 10.1016/j.bmc.2013.08.044. Epub 2013 Sep 4. Bioorg Med Chem. 2013. PMID: 24055078

10

Carbohydrate transition state mimics: synthesis of imidazolo-pyrrolidinoses as potential nectrisine surrogates.

Tschamber T, Gessier F, Dubost E, Newsome J, Tarnus C, Kohler J, Neuburger M, Streith J. Tschamber T, et al. Among authors: tarnus c. Bioorg Med Chem. 2003 Aug 15;11(17):3559-68. doi: 10.1016/s0968-0896(03)00402-4. Bioorg Med Chem. 2003. PMID: 12901900

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