Kang JS - Search Results

1

Exploring structural and biological insights of TEAD through rational design and synthesis of niflumic acid derivatives.

Choi YS, Kim YJ, Jeon Y, Kang JS, Lee J, Hong E, Park YH, Kim W, Cha B, Jeon R. Choi YS, et al. Among authors: kang js. J Enzyme Inhib Med Chem. 2024 Dec;39(1):2419925. doi: 10.1080/14756366.2024.2419925. Epub 2024 Nov 4. J Enzyme Inhib Med Chem. 2024. PMID: 39494490 Free PMC article.

2

Design and synthesis of novel benzoxazole analogs as Aurora B kinase inhibitors.

An Y, Lee E, Yu Y, Yun J, Lee MY, Kang JS, Kim WY, Jeon R. An Y, et al. Among authors: kang js. Bioorg Med Chem Lett. 2016 Jul 1;26(13):3067-3072. doi: 10.1016/j.bmcl.2016.05.017. Epub 2016 May 7. Bioorg Med Chem Lett. 2016. PMID: 27209235

3

Discovery of 5-Phenoxy-2-aminopyridine Derivatives as Potent and Selective Irreversible Inhibitors of Bruton's Tyrosine Kinase.

Lee E, Cho H, Lee DK, Ha J, Choi BJ, Jeong JH, Ryu JH, Kang JS, Jeon R. Lee E, et al. Among authors: kang js. Int J Mol Sci. 2020 Oct 28;21(21):8006. doi: 10.3390/ijms21218006. Int J Mol Sci. 2020. PMID: 33126415 Free PMC article.

4

Discovery of organosulfur-based selective HDAC8 inhibitors with anti-neuroblastoma activity.

Cho H, Lee E, Kim J, Shin S, Kim YJ, Lee H, Yu JH, Jeon YH, Lee SW, Lee SY, Park KW, Kang JS, Kwon SH, Kim Y, Jeon R. Cho H, et al. Among authors: kang js. Eur J Pharm Sci. 2024 Dec 1;203:106921. doi: 10.1016/j.ejps.2024.106921. Epub 2024 Sep 30. Eur J Pharm Sci. 2024. PMID: 39357770 Free article.

5

(E)-N'-Arylidene-2-(4-oxoquinazolin-4(3H)-yl) acetohydrazides: Synthesis and evaluation of antitumor cytotoxicity and caspase activation activity.

Huan LC, Phuong CV, Truc LC, Thanh VN, Pham-The H, Huong LT, Thuan NT, Park EJ, Ji AY, Kang JS, Han SB, Tran PT, Nam NH. Huan LC, et al. Among authors: kang js. J Enzyme Inhib Med Chem. 2019 Dec;34(1):465-478. doi: 10.1080/14756366.2018.1555536. J Enzyme Inhib Med Chem. 2019. PMID: 30734614 Free PMC article.

6

Design, synthesis, and evaluation of novel N'-substituted-1-(4-chlorobenzyl)-1H-indol-3-carbohydrazides as antitumor agents.

Huan LC, Anh DT, Hai PT, Anh LD, Park EJ, Ji AY, Kang JS, Dung DTM, Oanh DTK, Tung TT, Hai DTT, Han SB, Nam NH. Huan LC, et al. Among authors: kang js. J Enzyme Inhib Med Chem. 2020 Dec;35(1):1854-1865. doi: 10.1080/14756366.2020.1816997. J Enzyme Inhib Med Chem. 2020. PMID: 32981382 Free PMC article.

7

Design, synthesis, and biological evaluation of potent 1,2,3,4-tetrahydroisoquinoline derivatives as anticancer agents targeting NF-κB signaling pathway.

Sim S, Lee S, Ko S, Phuong Bui B, Linh Nguyen P, Cho J, Lee K, Kang JS, Jung JK, Lee H. Sim S, et al. Among authors: kang js. Bioorg Med Chem. 2021 Sep 15;46:116371. doi: 10.1016/j.bmc.2021.116371. Epub 2021 Aug 18. Bioorg Med Chem. 2021. PMID: 34500188

8

Structure-activity relationship of indoline-2-carboxylic acid N-(substituted)phenylamide derivatives.

Kwak JH, Kim Y, Park H, Jang JY, Lee KK, Yi W, Kwak JA, Park SG, Kim H, Lee K, Kang JS, Han SB, Hwang BY, Hong JT, Jung JK, Kim Y, Cho J, Lee H. Kwak JH, et al. Among authors: kang js. Bioorg Med Chem Lett. 2010 Aug 1;20(15):4620-3. doi: 10.1016/j.bmcl.2010.06.004. Epub 2010 Jun 8. Bioorg Med Chem Lett. 2010. PMID: 20579876

9

Structure-activity relationship studies of a series of novel delta-lactam-based histone deacetylase inhibitors.

Kim HM, Ryu DK, Choi Y, Park BW, Lee K, Han SB, Lee CW, Kang MR, Kang JS, Boovanahalli SK, Park SK, Han JW, Chun TG, Lee HY, Nam KY, Choi EH, Han G. Kim HM, et al. Among authors: kang js, kang mr. J Med Chem. 2007 May 31;50(11):2737-41. doi: 10.1021/jm0613828. Epub 2007 May 4. J Med Chem. 2007. PMID: 17477518

10

Modification of cap group in delta-lactam-based histone deacetylase (HDAC) inhibitors.

Kim HM, Hong SH, Kim MS, Lee CW, Kang JS, Lee K, Park SK, Han JW, Lee HY, Choi Y, Kwon HJ, Han G. Kim HM, et al. Among authors: kang js. Bioorg Med Chem Lett. 2007 Nov 15;17(22):6234-8. doi: 10.1016/j.bmcl.2007.09.034. Epub 2007 Sep 11. Bioorg Med Chem Lett. 2007. PMID: 17904843

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