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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 4 |
2011 | 2 |
2012 | 1 |
2024 | 0 |
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7 results
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Page 1
Synthesis and evaluation of 1-amino-6-halo-β-carbolines as antimalarial and antiprion agents.
ChemMedChem. 2012 Apr;7(4):578-86. doi: 10.1002/cmdc.201200002. Epub 2012 Jan 24.
ChemMedChem. 2012.
PMID: 22275299
2,4-diarylthiazole antiprion compounds as a novel structural class of antimalarial leads.
Thompson MJ, Louth JC, Little SM, Chen B, Coldham I.
Thompson MJ, et al.
Bioorg Med Chem Lett. 2011 Jun 15;21(12):3644-7. doi: 10.1016/j.bmcl.2011.04.090. Epub 2011 Apr 28.
Bioorg Med Chem Lett. 2011.
PMID: 21570837
Item in Clipboard
Exploring catalyst and solvent effects in the multicomponent synthesis of pyridine-3,5-dicarbonitriles.
Guo K, Thompson MJ, Chen B.
Guo K, et al.
J Org Chem. 2009 Sep 18;74(18):6999-7006. doi: 10.1021/jo901232b.
J Org Chem. 2009.
PMID: 19678630
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Ugi reactions with ammonia offer rapid access to a wide range of 5-aminothiazole and oxazole derivatives.
Thompson MJ, Chen B.
Thompson MJ, et al.
J Org Chem. 2009 Sep 18;74(18):7084-93. doi: 10.1021/jo9014529.
J Org Chem. 2009.
PMID: 19705810
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Structure-activity relationship refinement and further assessment of indole-3-glyoxylamides as a lead series against prion disease.
Thompson MJ, Louth JC, Ferrara S, Sorrell FJ, Irving BJ, Cochrane EJ, Meijer AJ, Chen B.
Thompson MJ, et al.
ChemMedChem. 2011 Jan 3;6(1):115-30. doi: 10.1002/cmdc.201000383.
ChemMedChem. 2011.
PMID: 21154498
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Design, synthesis, and structure-activity relationship of indole-3-glyoxylamide libraries possessing highly potent activity in a cell line model of prion disease.
Thompson MJ, Borsenberger V, Louth JC, Judd KE, Chen B.
Thompson MJ, et al.
J Med Chem. 2009 Dec 10;52(23):7503-11. doi: 10.1021/jm900920x.
J Med Chem. 2009.
PMID: 19842664
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Development of a diversity-oriented approach to oxazole-5-amide libraries.
Thompson MJ, Adams H, Chen B.
Thompson MJ, et al.
J Org Chem. 2009 May 15;74(10):3856-65. doi: 10.1021/jo900425w.
J Org Chem. 2009.
PMID: 19374383
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