Lee ES - Search Results

1

Convenient synthesis of indeno[1,2-c]isoquinolines as constrained forms of 3-arylisoquinolines and docking study of a topoisomerase I inhibitor into DNA-topoisomerase I complex.

Van HT, Le QM, Lee KY, Lee ES, Kwon Y, Kim TS, Le TN, Lee SH, Cho WJ. Van HT, et al. Among authors: lee sh, lee ky, lee es. Bioorg Med Chem Lett. 2007 Nov 1;17(21):5763-7. doi: 10.1016/j.bmcl.2007.08.062. Epub 2007 Aug 29. Bioorg Med Chem Lett. 2007. PMID: 17827007

2

Molecular modeling of 3-arylisoquinoline antitumor agents active against A-549. A comparative molecular field analysis study.

Cho WJ, Kim EK, Park IY, Jeong EY, Kim TS, Le TN, Kim DD, Lee ES. Cho WJ, et al. Among authors: lee es. Bioorg Med Chem. 2002 Sep;10(9):2953-61. doi: 10.1016/s0968-0896(02)00137-2. Bioorg Med Chem. 2002. PMID: 12110317

3

Synthesis, topoisomerase I inhibition and structure-activity relationship study of 2,4,6-trisubstituted pyridine derivatives.

Zhao LX, Moon YS, Basnet A, Kim EK, Jahng Y, Park JG, Jeong TC, Cho WJ, Choi SU, Lee CO, Lee SY, Lee CS, Lee ES. Zhao LX, et al. Among authors: lee sy, lee co, lee es, lee cs. Bioorg Med Chem Lett. 2004 Mar 8;14(5):1333-7. doi: 10.1016/j.bmcl.2003.11.084. Bioorg Med Chem Lett. 2004. PMID: 14980693

4

Simple aromatic compounds containing propenone moiety show considerable dual COX/5-LOX inhibitory activities.

Jahng Y, Zhao LX, Moon YS, Basnet A, Kim EK, Chang HW, Ju HK, Jeong TC, Lee ES. Jahng Y, et al. Among authors: lee es. Bioorg Med Chem Lett. 2004 May 17;14(10):2559-62. doi: 10.1016/j.bmcl.2004.02.099. Bioorg Med Chem Lett. 2004. PMID: 15109651

5

Synthesis, cytotoxicity and structure-activity relationship study of terpyridines.

Zhao LX, Sherchan J, Park JK, Jahng Y, Jeong BS, Jeong TC, Lee CS, Lee ES. Zhao LX, et al. Among authors: lee es, lee cs. Arch Pharm Res. 2006 Dec;29(12):1091-5. doi: 10.1007/BF02969297. Arch Pharm Res. 2006. PMID: 17225456

6

2,4,6-Trisubstituted pyridines: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship.

Basnet A, Thapa P, Karki R, Na Y, Jahng Y, Jeong BS, Jeong TC, Lee CS, Lee ES. Basnet A, et al. Among authors: lee es, lee cs. Bioorg Med Chem. 2007 Jul 1;15(13):4351-9. doi: 10.1016/j.bmc.2007.04.047. Epub 2007 Apr 29. Bioorg Med Chem. 2007. PMID: 17493824

7

Design, docking, and synthesis of novel indeno[1,2-c]isoquinolines for the development of antitumor agents as topoisomerase I inhibitors.

Cho WJ, Le QM, My Van HT, Youl Lee K, Kang BY, Lee ES, Lee SK, Kwon Y. Cho WJ, et al. Among authors: lee sk, lee es. Bioorg Med Chem Lett. 2007 Jul 1;17(13):3531-4. doi: 10.1016/j.bmcl.2007.04.064. Epub 2007 Apr 25. Bioorg Med Chem Lett. 2007. PMID: 17498951

8

Synthesis of 2,6-diaryl-substituted pyridines and their antitumor activities.

Son JK, Zhao LX, Basnet A, Thapa P, Karki R, Na Y, Jahng Y, Jeong TC, Jeong BS, Lee CS, Lee ES. Son JK, et al. Among authors: lee es, lee cs. Eur J Med Chem. 2008 Apr;43(4):675-82. doi: 10.1016/j.ejmech.2007.05.002. Epub 2007 May 27. Eur J Med Chem. 2008. PMID: 17673337

9

New insight for fluoroquinophenoxazine derivatives as possibly new potent topoisomerase I inhibitor.

Kang DH, Kim JS, Jung MJ, Lee ES, Jahng Y, Kwon Y, Na Y. Kang DH, et al. Among authors: lee es. Bioorg Med Chem Lett. 2008 Feb 15;18(4):1520-4. doi: 10.1016/j.bmcl.2007.12.053. Epub 2007 Dec 25. Bioorg Med Chem Lett. 2008. PMID: 18178085

10

2-Thienyl-4-furyl-6-aryl pyridine derivatives: synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study.

Thapa P, Karki R, Thapa U, Jahng Y, Jung MJ, Nam JM, Na Y, Kwon Y, Lee ES. Thapa P, et al. Among authors: lee es. Bioorg Med Chem. 2010 Jan 1;18(1):377-86. doi: 10.1016/j.bmc.2009.10.049. Epub 2009 Oct 29. Bioorg Med Chem. 2010. PMID: 19939682

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