Blonski C - Search Results

1

Structural flexibility in Trypanosoma brucei enolase revealed by X-ray crystallography and molecular dynamics.

de A S Navarro MV, Gomes Dias SM, Mello LV, da Silva Giotto MT, Gavalda S, Blonski C, Garratt RC, Rigden DJ. de A S Navarro MV, et al. Among authors: blonski c. FEBS J. 2007 Oct;274(19):5077-89. doi: 10.1111/j.1742-4658.2007.06027.x. Epub 2007 Sep 5. FEBS J. 2007. PMID: 17822439 Free article.

2

N-Sulfonyl hydroxamate derivatives as inhibitors of class II fructose-1,6-diphosphate aldolase.

Gavalda S, Braga R, Dax C, Vigroux A, Blonski C. Gavalda S, et al. Among authors: blonski c. Bioorg Med Chem Lett. 2005 Dec 15;15(24):5375-7. doi: 10.1016/j.bmcl.2005.09.006. Epub 2005 Oct 19. Bioorg Med Chem Lett. 2005. PMID: 16236509

3

Selective irreversible inhibition of fructose 1,6-bisphosphate aldolase from Trypanosoma brucei.

Dax C, Duffieux F, Chabot N, Coincon M, Sygusch J, Michels PA, Blonski C. Dax C, et al. Among authors: blonski c. J Med Chem. 2006 Mar 9;49(5):1499-502. doi: 10.1021/jm050237b. J Med Chem. 2006. PMID: 16509566

4

Cell permeation of a Trypanosoma brucei aldolase inhibitor: evaluation of different enzyme-labile phosphate protecting groups.

Azéma L, Lherbet C, Baudoin C, Blonski C. Azéma L, et al. Among authors: blonski c. Bioorg Med Chem Lett. 2006 Jul 1;16(13):3440-3. doi: 10.1016/j.bmcl.2006.04.010. Epub 2006 Apr 24. Bioorg Med Chem Lett. 2006. PMID: 16632348

5

New potent bisubstrate inhibitors of histone acetyltransferase p300: design, synthesis and biological evaluation.

Kwie FH, Briet M, Soupaya D, Hoffmann P, Maturano M, Rodriguez F, Blonski C, Lherbet C, Baudoin-Dehoux C. Kwie FH, et al. Among authors: blonski c. Chem Biol Drug Des. 2011 Jan;77(1):86-92. doi: 10.1111/j.1747-0285.2010.01056.x. Epub 2010 Nov 30. Chem Biol Drug Des. 2011. PMID: 21118378

6

Irreversible inhibition of aldolase by a phosphorylated alpha-dicarbonyl compound.

Chabot N, Vinatier V, Gefflaut T, Baudoin C, Rodriguez F, Blonski C, Hoffmann P. Chabot N, et al. Among authors: blonski c. J Enzyme Inhib Med Chem. 2008 Feb;23(1):21-7. doi: 10.1080/14756360701383718. J Enzyme Inhib Med Chem. 2008. PMID: 18341248 Free article.

7

Hydroxynaphthaldehyde phosphate derivatives as potent covalent Schiff base inhibitors of fructose-1,6-bisphosphate aldolase.

Dax C, Coinçon M, Sygusch J, Blonski C. Dax C, et al. Among authors: blonski c. Biochemistry. 2005 Apr 12;44(14):5430-43. doi: 10.1021/bi0477992. Biochemistry. 2005. PMID: 15807536

8

Glycolysis and proteases as targets for the design of new anti-trypanosome drugs.

Lakhdar-Ghazal F, Blonski C, Willson M, Michels P, Perie J. Lakhdar-Ghazal F, et al. Among authors: blonski c. Curr Top Med Chem. 2002 May;2(5):439-56. doi: 10.2174/1568026024607472. Curr Top Med Chem. 2002. PMID: 11966466 Review.

9

Charge stabilization and entropy reduction of central lysine residues in fructose-bisphosphate aldolase.

St-Jean M, Blonski C, Sygusch J. St-Jean M, et al. Among authors: blonski c. Biochemistry. 2009 Jun 2;48(21):4528-37. doi: 10.1021/bi8021558. Biochemistry. 2009. PMID: 19354220

10

Inhibition of rabbit muscle aldolase by phosphorylated aromatic compounds.

Blonski C, De Moissac D, Périé J, Sygusch J. Blonski C, et al. Biochem J. 1997 Apr 1;323 ( Pt 1)(Pt 1):71-7. doi: 10.1042/bj3230071. Biochem J. 1997. PMID: 9173904 Free PMC article.

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