Jeong Y - Search Results

1

Identification of β-Lapachone Analogs as Novel MALT1 Inhibitors To Treat an Aggressive Subtype of Diffuse Large B-Cell Lymphoma.

Lim SM, Jeong Y, Lee S, Im H, Tae HS, Kim BG, Park HD, Park J, Hong S. Lim SM, et al. Among authors: jeong y. J Med Chem. 2015 Nov 12;58(21):8491-502. doi: 10.1021/acs.jmedchem.5b01415. Epub 2015 Oct 29. J Med Chem. 2015. PMID: 26496175

2

Design and synthesis of imidazopyridine analogues as inhibitors of phosphoinositide 3-kinase signaling and angiogenesis.

Kim O, Jeong Y, Lee H, Hong SS, Hong S. Kim O, et al. Among authors: jeong y. J Med Chem. 2011 Apr 14;54(7):2455-66. doi: 10.1021/jm101582z. Epub 2011 Mar 9. J Med Chem. 2011. PMID: 21388141

3

Selective and potent small-molecule inhibitors of PI3Ks.

Jeong Y, Kwon D, Hong S. Jeong Y, et al. Future Med Chem. 2014 May;6(7):737-56. doi: 10.4155/fmc.14.28. Future Med Chem. 2014. PMID: 24941870 Review.

4

Discovery of wrightiadione as a novel template for the TrkA kinase inhibitors.

Jeong Y, Lim SM, Hong S. Jeong Y, et al. Bioorg Med Chem Lett. 2015 Nov 15;25(22):5186-9. doi: 10.1016/j.bmcl.2015.09.070. Epub 2015 Sep 30. Bioorg Med Chem Lett. 2015. PMID: 26442778

5

Strategies to overcome acquired resistances conferred by mutations in the kinase domain of EGFR.

Lim SM, Jeong Y, Hong S. Lim SM, et al. Among authors: jeong y. Future Med Chem. 2016 May;8(8):853-78. doi: 10.4155/fmc-2016-0019. Epub 2016 May 19. Future Med Chem. 2016. PMID: 27195594 Review.

6

Structure-based de novo design and biochemical evaluation of novel BRAF kinase inhibitors.

Park H, Jeong Y, Hong S. Park H, et al. Among authors: jeong y. Bioorg Med Chem Lett. 2012 Jan 15;22(2):1027-30. doi: 10.1016/j.bmcl.2011.11.124. Epub 2011 Dec 7. Bioorg Med Chem Lett. 2012. PMID: 22196123

7

Rh(III)-catalyzed direct C-H/C-H cross-coupling of quinones with arenes assisted by a directing group: identification of carbazole quinones as GSKβ inhibitors.

Moon Y, Jeong Y, Kook D, Hong S. Moon Y, et al. Among authors: jeong y. Org Biomol Chem. 2015 Apr 7;13(13):3918-23. doi: 10.1039/c4ob02624a. Org Biomol Chem. 2015. PMID: 25708198

8

Ru(II)-Catalyzed Site-Selective Hydroxylation of Flavone and Chromone Derivatives: The Importance of the 5-Hydroxyl Motif for the Inhibition of Aurora Kinases.

Kim K, Choe H, Jeong Y, Lee JH, Hong S. Kim K, et al. Among authors: jeong y. Org Lett. 2015 May 15;17(10):2550-3. doi: 10.1021/acs.orglett.5b01138. Epub 2015 May 6. Org Lett. 2015. PMID: 25946086

9

Selectivity enhancement arising from interactions at the PI3K unique pocket.

Jeong Y, Lee J, Lee Y, Ham K, Choi S, Hong S. Jeong Y, et al. ChemMedChem. 2012 Aug;7(8):1379-83. doi: 10.1002/cmdc.201200245. Epub 2012 Jun 22. ChemMedChem. 2012. PMID: 22730062 No abstract available.

10

Tandem Dehydrogenation/Oxidation/Oxidative Cyclization Approach to Wrightiadione and Its Derivatives.

Jeong Y, Moon Y, Hong S. Jeong Y, et al. Org Lett. 2015 Jul 2;17(13):3252-5. doi: 10.1021/acs.orglett.5b01618. Epub 2015 Jun 19. Org Lett. 2015. PMID: 26090926

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