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David K. Jung

Research Triangle Park

15

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821

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Corrigendum to “(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors” [Bioorg. Med. Chem. Lett. 15 (2005) 3402–3406]

2015 Bioorganic & Medicinal Chemistry Letters
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The identification of pyrazolo[1,5-a]pyridines as potent p38 kinase inhibitors

2008 Bioorganic & Medicinal Chemistry Letters
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Development of dihydropyridone indazole amides as selective Rho-kinase inhibitors.

2007 Journal of Medicinal Chemistry
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Discovery of Aminofurazan-azabenzimidazoles as Inhibitors of Rho-Kinase with High Kinase Selectivity and Antihypertensive Activity

2007 Journal of Medicinal Chemistry
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Discovery and in vitro evaluation of potent kinase inhibitors: Pyrido[1',2':1,5]pyrazolo[3,4-d]pyrimidines.

2005 Bioorganic & Medicinal Chemistry Letters
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(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors

2005 Bioorganic & Medicinal Chemistry Letters
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Derivatives of 5- (acylamino) indazole as kinase inhibitors.

2004
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Pyrazolo[1,5-a]pyridines: synthetic approaches to a novel class of antiherpetics

2003 Tetrahedron
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Identification and structure-activity studies of novel ultrashort-acting benzodiazepine receptor agonists

2002 Bioorganic & Medicinal Chemistry Letters
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The discovery of potent cRaf1 kinase inhibitors.

2000 Bioorganic & Medicinal Chemistry Letters
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Citations (189)