Ko H - Search Results

1

RUNX3 confers sensitivity to pheophorbide a-photodynamic therapy in human oral squamous cell carcinoma cell lines.

Moon S, Bae JY, Son HK, Lee DY, Park G, You H, Ko H, Kim YC, Kim J. Moon S, et al. Among authors: ko h. Lasers Med Sci. 2015 Feb;30(2):499-507. doi: 10.1007/s10103-013-1350-1. Epub 2013 May 23. Lasers Med Sci. 2015. PMID: 23700080

2

Pheophorbide-a conjugates with cancer-targeting moieties for targeted photodynamic cancer therapy.

You H, Yoon HE, Jeong PH, Ko H, Yoon JH, Kim YC. You H, et al. Among authors: ko h. Bioorg Med Chem. 2015 Apr 1;23(7):1453-62. doi: 10.1016/j.bmc.2015.02.014. Epub 2015 Feb 16. Bioorg Med Chem. 2015. PMID: 25753328

3

Synthesis of pheophorbide-a conjugates with anticancer drugs as potential cancer diagnostic and therapeutic agents.

You H, Yoon HE, Yoon JH, Ko H, Kim YC. You H, et al. Among authors: ko h. Bioorg Med Chem. 2011 Sep 15;19(18):5383-91. doi: 10.1016/j.bmc.2011.07.058. Epub 2011 Aug 2. Bioorg Med Chem. 2011. PMID: 21873067

4

Design, synthesis and X-ray crystallographic study of NAmPRTase inhibitors as anti-cancer agents.

You H, Youn HS, Im I, Bae MH, Lee SK, Ko H, Eom SH, Kim YC. You H, et al. Among authors: ko h. Eur J Med Chem. 2011 Apr;46(4):1153-64. doi: 10.1016/j.ejmech.2011.01.034. Epub 2011 Jan 31. Eur J Med Chem. 2011. PMID: 21330015

5

Solid-phase synthesis of quinolinone library.

Kwak SH, Kim MJ, Lee SD, You H, Kim YC, Ko H. Kwak SH, et al. Among authors: ko h. ACS Comb Sci. 2015 Jan 12;17(1):60-9. doi: 10.1021/co5001585. Epub 2014 Dec 1. ACS Comb Sci. 2015. PMID: 25437883

6

Structure-activity relationship studies of pyrimidine-2,4-dione derivatives as potent P2X7 receptor antagonists.

Park JH, Lee GE, Lee SD, Ko H, Kim YC. Park JH, et al. Among authors: ko h. Eur J Med Chem. 2015 Dec 1;106:180-93. doi: 10.1016/j.ejmech.2015.10.036. Epub 2015 Oct 23. Eur J Med Chem. 2015. PMID: 26547056

7

Synthesis and structure-activity relationships of pyrazolodiazepine derivatives as human P2X7 receptor antagonists.

Lee JY, Yu J, Cho WJ, Ko H, Kim YC. Lee JY, et al. Among authors: ko h. Bioorg Med Chem Lett. 2009 Nov 1;19(21):6053-8. doi: 10.1016/j.bmcl.2009.09.053. Epub 2009 Sep 17. Bioorg Med Chem Lett. 2009. PMID: 19800793

8

Design and synthesis of potent and selective P2X₃ receptor antagonists derived from PPADS as potential pain modulators.

Cho JH, Jung KY, Jung Y, Kim MH, Ko H, Park CS, Kim YC. Cho JH, et al. Among authors: ko h. Eur J Med Chem. 2013;70:811-30. doi: 10.1016/j.ejmech.2013.10.026. Epub 2013 Oct 18. Eur J Med Chem. 2013. PMID: 24246730

9

Discovery of novel purine-based heterocyclic P2X7 receptor antagonists.

Kwak SH, Lee WG, Lee YJ, Lee SD, Kim YC, Ko H. Kwak SH, et al. Among authors: ko h. Bioorg Chem. 2015 Aug;61:58-65. doi: 10.1016/j.bioorg.2015.06.003. Epub 2015 Jun 20. Bioorg Chem. 2015. PMID: 26123174

10

Synthesis and structure-activity relationships of quinolinone and quinoline-based P2X7 receptor antagonists and their anti-sphere formation activities in glioblastoma cells.

Kwak SH, Shin S, Lee JH, Shim JK, Kim M, Lee SD, Lee A, Bae J, Park JH, Abdelrahman A, Müller CE, Cho SK, Kang SG, Bae MA, Yang JY, Ko H, Goddard WA 3rd, Kim YC. Kwak SH, et al. Among authors: ko h. Eur J Med Chem. 2018 May 10;151:462-481. doi: 10.1016/j.ejmech.2018.03.023. Epub 2018 Mar 9. Eur J Med Chem. 2018. PMID: 29649742

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