Ha JD - Search Results

1

KRC-327, a selective novel inhibitor of c-Met receptor tyrosine kinase with anticancer activity.

Park BH, Jung KH, Yun SM, Hong SW, Ryu JW, Jung H, Ha JD, Lee J, Hong SS. Park BH, et al. Among authors: ha jd. Cancer Lett. 2013 May 1;331(2):158-66. doi: 10.1016/j.canlet.2012.12.025. Epub 2013 Jan 20. Cancer Lett. 2013. PMID: 23340177

2

Design and synthesis of triazolopyridazines substituted with methylisoquinolinone as selective c-Met kinase inhibitors.

Ryu JW, Han SY, Yun JI, Choi SU, Jung H, Ha JD, Cho SY, Lee CO, Kang NS, Koh JS, Kim HR, Lee J. Ryu JW, et al. Among authors: ha jd. Bioorg Med Chem Lett. 2011 Dec 1;21(23):7185-8. doi: 10.1016/j.bmcl.2011.09.066. Epub 2011 Sep 22. Bioorg Med Chem Lett. 2011. PMID: 22001029

3

Discovery of aminopyridines substituted with benzoxazole as orally active c-Met kinase inhibitors.

Cho SY, Han SY, Ha JD, Ryu JW, Lee CO, Jung H, Kang NS, Kim HR, Koh JS, Lee J. Cho SY, et al. Among authors: ha jd. Bioorg Med Chem Lett. 2010 Jul 15;20(14):4223-7. doi: 10.1016/j.bmcl.2010.05.031. Epub 2010 May 15. Bioorg Med Chem Lett. 2010. PMID: 20570511

4

Evaluation of a multi-kinase inhibitor KRC-108 as an anti-tumor agent in vitro and in vivo.

Han SY, Lee CO, Ahn SH, Lee MO, Kang SY, Cha HJ, Cho SY, Ha JD, Ryu JW, Jung H, Kim HR, Koh JS, Lee J. Han SY, et al. Among authors: ha jd. Invest New Drugs. 2012 Apr;30(2):518-23. doi: 10.1007/s10637-010-9584-2. Epub 2010 Nov 16. Invest New Drugs. 2012. PMID: 21080208

5

Synthesis and structure-activity relationship of aminopyridines with substituted benzoxazoles as c-Met kinase inhibitors.

Lee J, Han SY, Jung H, Yang J, Choi JW, Chae CH, Park CH, Choi SU, Lee K, Ha JD, Lee CO, Ryu JW, Kim HR, Koh JS, Cho SY. Lee J, et al. Among authors: ha jd. Bioorg Med Chem Lett. 2012 Jun 15;22(12):4044-8. doi: 10.1016/j.bmcl.2012.04.083. Epub 2012 Apr 25. Bioorg Med Chem Lett. 2012. PMID: 22579487

6

Novel c-Met inhibitor suppresses the growth of c-Met-addicted gastric cancer cells.

Park CH, Cho SY, Ha JD, Jung H, Kim HR, Lee CO, Jang IY, Chae CH, Lee HK, Choi SU. Park CH, et al. Among authors: ha jd. BMC Cancer. 2016 Jan 22;16:35. doi: 10.1186/s12885-016-2058-y. BMC Cancer. 2016. PMID: 26801760 Free PMC article.

7

Design and synthesis of 3-(4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridin-2-yl)-1H-quinolin-2-ones as VEGFR-2 kinase inhibitors.

Han SY, Choi JW, Yang J, Chae CH, Lee J, Jung H, Lee K, Ha JD, Kim HR, Cho SY. Han SY, et al. Among authors: ha jd. Bioorg Med Chem Lett. 2012 Apr 15;22(8):2837-42. doi: 10.1016/j.bmcl.2012.02.073. Epub 2012 Mar 7. Bioorg Med Chem Lett. 2012. PMID: 22450128

8

Design and synthesis of novel 3-(benzo[d]oxazol-2-yl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)pyridin-2-amine derivatives as selective G-protein-coupled receptor kinase-2 and -5 inhibitors.

Cho SY, Lee BH, Jung H, Yun CS, Ha JD, Kim HR, Chae CH, Lee JH, Seo HW, Oh KS. Cho SY, et al. Among authors: ha jd. Bioorg Med Chem Lett. 2013 Dec 15;23(24):6711-6. doi: 10.1016/j.bmcl.2013.10.036. Epub 2013 Oct 30. Bioorg Med Chem Lett. 2013. PMID: 24210504

9

Synthesis and evaluation of novel 2,4-diaminopyrimidines bearing bicyclic aminobenzazepines for anaplastic lymphoma kinase (ALK) inhibitor.

Kang GA, Lee M, Song D, Lee HK, Ahn S, Park CH, Lee CO, Yun CS, Jung H, Kim P, Ha JD, Cho SY, Kim HR, Hwang JY. Kang GA, et al. Among authors: ha jd. Bioorg Med Chem Lett. 2015 Sep 15;25(18):3992-8. doi: 10.1016/j.bmcl.2015.07.004. Epub 2015 Jul 17. Bioorg Med Chem Lett. 2015. PMID: 26235945

10

Novel bis-ortho-alkoxy-para-piperazinesubstituted-2,4-dianilinopyrimidines (KRCA-0008) as potent and selective ALK inhibitors for anticancer treatment.

Park CH, Choe H, Jang IY, Kwon SY, Latif M, Lee HK, Lee HJ, Yang EH, Yun JI, Chae CH, Cho SY, Choi SU, Ha JD, Jung H, Kim HR, Kim P, Lee CO, Yun CS, Lee K. Park CH, et al. Among authors: ha jd. Bioorg Med Chem Lett. 2013 Nov 15;23(22):6192-6. doi: 10.1016/j.bmcl.2013.08.090. Epub 2013 Sep 4. Bioorg Med Chem Lett. 2013. PMID: 24095090

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