Lee K - Search Results

1

Glutaminase inhibition as potential cancer therapeutics: current status and future applications.

Cyriac R, Lee K. Cyriac R, et al. Among authors: lee k. J Enzyme Inhib Med Chem. 2024 Dec;39(1):2290911. doi: 10.1080/14756366.2023.2290911. Epub 2023 Dec 11. J Enzyme Inhib Med Chem. 2024. PMID: 38078371 Review.

2

Novel allosteric glutaminase 1 inhibitors with macrocyclic structure activity relationship analysis.

Lee EJ, Duggirala KB, Lee Y, Yun MR, Jang J, Cyriac R, Jung ME, Choi G, Chae CH, Cho BC, Lee K. Lee EJ, et al. Among authors: lee y, lee k. Bioorg Med Chem Lett. 2022 Nov 1;75:128956. doi: 10.1016/j.bmcl.2022.128956. Epub 2022 Aug 28. Bioorg Med Chem Lett. 2022. PMID: 36038117 Free article.

3

First macrocyclic 3^rd-generation ALK inhibitor for treatment of ALK/ROS1 cancer: Clinical and designing strategy update of lorlatinib.

Basit S, Ashraf Z, Lee K, Latif M. Basit S, et al. Among authors: lee k. Eur J Med Chem. 2017 Jul 7;134:348-356. doi: 10.1016/j.ejmech.2017.04.032. Epub 2017 Apr 13. Eur J Med Chem. 2017. PMID: 28431340 Review.

4

Discovery of novel [1,2,4]triazolo[4,3-a]quinoxaline aminophenyl derivatives as BET inhibitors for cancer treatment.

Ali I, Lee J, Go A, Choi G, Lee K. Ali I, et al. Among authors: lee k, lee j. Bioorg Med Chem Lett. 2017 Oct 15;27(20):4606-4613. doi: 10.1016/j.bmcl.2017.09.025. Epub 2017 Sep 14. Bioorg Med Chem Lett. 2017. PMID: 28939121

5

Development and structure-activity relationship study of SHP2 inhibitor containing 3,4,6-trihydroxy-5-oxo-5H-benzo[7]annulene.

Kim B, Jo S, Park SB, Chae CH, Lee K, Koh B, Shin I. Kim B, et al. Among authors: lee k. Bioorg Med Chem Lett. 2020 Jan 1;30(1):126756. doi: 10.1016/j.bmcl.2019.126756. Epub 2019 Nov 11. Bioorg Med Chem Lett. 2020. PMID: 31784318

6

DW71177: A novel [1,2,4]triazolo[4,3-a]quinoxaline-based potent and BD1-Selective BET inhibitor for the treatment of acute myeloid leukemia.

Ali I, Cha HJ, Lim B, Chae CH, Youm J, Park WJ, Lee SH, Kim JH, Jeong D, Lim JK, Hwang YH, Roe JS, Woo JS, Lee K, Choi G. Ali I, et al. Among authors: lee sh, lee k. Eur J Med Chem. 2024 Feb 5;265:116052. doi: 10.1016/j.ejmech.2023.116052. Epub 2023 Dec 16. Eur J Med Chem. 2024. PMID: 38134745 Free 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: lee k, lee j. 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

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: lee k, lee co. 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

9

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: lee k, lee co, lee hk, lee hj. 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

10

Discovery of indirubin derivatives as new class of DRAK2 inhibitors from high throughput screening.

Jung ME, Byun BJ, Kim HM, Lee JY, Park JH, Lee N, Son YH, Choi SU, Yang KM, Kim SJ, Lee K, Kim YC, Choi G. Jung ME, et al. Among authors: lee k, lee jy, lee n. Bioorg Med Chem Lett. 2016 Jun 1;26(11):2719-23. doi: 10.1016/j.bmcl.2016.03.111. Epub 2016 Apr 1. Bioorg Med Chem Lett. 2016. PMID: 27106709

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