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Recent progress in the design, study, and development of c-Jun N-terminal kinase inhibitors as anticancer agents.
Chem Biol. 2014 Nov 20;21(11):1433-43. doi: 10.1016/j.chembiol.2014.09.007. Epub 2014 Oct 16.
Chem Biol. 2014.
PMID: 25442375
Review.
Rational Design, Synthesis, and Biological Evaluation of 7-Azaindole Derivatives as Potent Focused Multi-Targeted Kinase Inhibitors.
Daydé-Cazals B, Fauvel B, Singer M, Feneyrolles C, Bestgen B, Gassiot F, Spenlinhauer A, Warnault P, Van Hijfte N, Borjini N, Chevé G, Yasri A.
Daydé-Cazals B, et al. Among authors: van hijfte n.
J Med Chem. 2016 Apr 28;59(8):3886-905. doi: 10.1021/acs.jmedchem.6b00087. Epub 2016 Apr 15.
J Med Chem. 2016.
PMID: 27010810
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Discovering novel 7-azaindole-based series as potent AXL kinase inhibitors.
Feneyrolles C, Guiet L, Singer M, Van Hijfte N, Daydé-Cazals B, Fauvel B, Chevé G, Yasri A.
Feneyrolles C, et al. Among authors: van hijfte n.
Bioorg Med Chem Lett. 2017 Feb 15;27(4):862-866. doi: 10.1016/j.bmcl.2017.01.015. Epub 2017 Jan 9.
Bioorg Med Chem Lett. 2017.
PMID: 28094183
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Addition of electrophilic radicals to 2-benzyloxyglycals: synthesis and functionalization of fluorinated α-C-glycosides and derivatives.
Colombel S, Van Hijfte N, Poisson T, Leclerc E, Pannecoucke X.
Colombel S, et al. Among authors: van hijfte n.
Chemistry. 2013 Sep 16;19(38):12778-87. doi: 10.1002/chem.201302070. Epub 2013 Aug 16.
Chemistry. 2013.
PMID: 23955898
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Indium-promoted diastereoselective addition of fluorinated haloallylic derivatives to imines.
Lemonnier G, Van Hijfte N, Poisson T, Couve-Bonnaire S, Pannecoucke X.
Lemonnier G, et al. Among authors: van hijfte n.
J Org Chem. 2014 Apr 4;79(7):2916-25. doi: 10.1021/jo402810s. Epub 2014 Mar 27.
J Org Chem. 2014.
PMID: 24620849
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