Na Y - Search Results

1

Study on the synthesis and cytotoxicity of new quinophenoxazine derivatives.

Kwon Y, Na Y. Kwon Y, et al. Among authors: na y. Chem Pharm Bull (Tokyo). 2006 Feb;54(2):248-51. doi: 10.1248/cpb.54.248. Chem Pharm Bull (Tokyo). 2006. PMID: 16462076 Free article.

2

Synthesis of new xanthone analogues and their biological activity test--cytotoxicity, topoisomerase II inhibition, and DNA cross-linking study.

Woo S, Jung J, Lee C, Kwon Y, Na Y. Woo S, et al. Among authors: na y. Bioorg Med Chem Lett. 2007 Mar 1;17(5):1163-6. doi: 10.1016/j.bmcl.2006.12.030. Epub 2006 Dec 13. Bioorg Med Chem Lett. 2007. PMID: 17194586

3

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: na y. 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

4

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: na y. 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

5

Identification of 3-acetyl-2-aminoquinolin-4-one as a novel, nonpeptidic scaffold for specific calpain inhibitory activity.

Kang DH, Jun KY, Lee JP, Pak CS, Na Y, Kwon Y. Kang DH, et al. Among authors: na y. J Med Chem. 2009 May 14;52(9):3093-7. doi: 10.1021/jm8014734. J Med Chem. 2009. PMID: 19419206

6

A concise synthesis of licochalcone E and its regio-isomer, licochalcone F.

Na Y, Cha JH, Yoon HG, Kwon Y. Na Y, et al. Chem Pharm Bull (Tokyo). 2009 Jun;57(6):607-9. doi: 10.1248/cpb.57.607. Chem Pharm Bull (Tokyo). 2009. PMID: 19483343 Free article.

7

Oxiranylmethyloxy or thiiranylmethyloxy-azaxanthones and -acridone analogues as potential topoisomerase I inhibitors.

Cho HJ, Jung MJ, Kwon Y, Na Y. Cho HJ, et al. Among authors: na y. Bioorg Med Chem Lett. 2009 Dec 1;19(23):6766-9. doi: 10.1016/j.bmcl.2009.09.091. Epub 2009 Sep 27. Bioorg Med Chem Lett. 2009. PMID: 19836231

8

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: na y. 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

9

2,6-Dithienyl-4-furyl pyridines: Synthesis, topoisomerase I and II inhibition, cytotoxicity, structure-activity relationship, and docking study.

Basnet A, Thapa P, Karki R, Choi H, Choi JH, Yun M, Jeong BS, Jahng Y, Na Y, Cho WJ, Kwon Y, Lee CS, Lee ES. Basnet A, et al. Among authors: na y. Bioorg Med Chem Lett. 2010 Jan 1;20(1):42-7. doi: 10.1016/j.bmcl.2009.11.041. Epub 2009 Nov 14. Bioorg Med Chem Lett. 2010. PMID: 19954977

10

New benzoxanthone derivatives as topoisomerase inhibitors and DNA cross-linkers.

Cho HJ, Jung MJ, Woo S, Kim J, Lee ES, Kwon Y, Na Y. Cho HJ, et al. Among authors: na y. Bioorg Med Chem. 2010 Feb;18(3):1010-7. doi: 10.1016/j.bmc.2009.12.069. Epub 2010 Jan 4. Bioorg Med Chem. 2010. PMID: 20093033

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