Kim JA - Search Results

1

Analogs of 5-(substituted benzylidene)hydantoin as inhibitors of tyrosinase and melanin formation.

Ha YM, Kim JA, Park YJ, Park D, Kim JM, Chung KW, Lee EK, Park JY, Lee JY, Lee HJ, Yoon JH, Moon HR, Chung HY. Ha YM, et al. Among authors: kim jm, kim ja. Biochim Biophys Acta. 2011 Jun;1810(6):612-9. doi: 10.1016/j.bbagen.2011.03.001. Epub 2011 Mar 21. Biochim Biophys Acta. 2011. PMID: 21397665

2

Synthesis and biological activity of hydroxy substituted phenyl-benzo[d]thiazole analogues for antityrosinase activity in B16 cells.

Ha YM, Park JY, Park YJ, Park D, Choi YJ, Kim JM, Lee EK, Han YK, Kim JA, Lee JY, Moon HR, Chung HY. Ha YM, et al. Among authors: kim jm, kim ja. Bioorg Med Chem Lett. 2011 Apr 15;21(8):2445-9. doi: 10.1016/j.bmcl.2011.02.064. Epub 2011 Feb 23. Bioorg Med Chem Lett. 2011. PMID: 21397499

3

Design, synthesis and biological evaluation of 2-(substituted phenyl)thiazolidine-4-carboxylic acid derivatives as novel tyrosinase inhibitors.

Ha YM, Park YJ, Lee JY, Park D, Choi YJ, Lee EK, Kim JM, Kim JA, Park JY, Lee HJ, Moon HR, Chung HY. Ha YM, et al. Among authors: kim jm, kim ja. Biochimie. 2012 Feb;94(2):533-40. doi: 10.1016/j.biochi.2011.09.002. Epub 2011 Sep 17. Biochimie. 2012. PMID: 21945595

4

Design and synthesis of 5-(substituted benzylidene)thiazolidine-2,4-dione derivatives as novel tyrosinase inhibitors.

Ha YM, Park YJ, Kim JA, Park D, Park JY, Lee HJ, Lee JY, Moon HR, Chung HY. Ha YM, et al. Among authors: kim ja. Eur J Med Chem. 2012 Mar;49:245-52. doi: 10.1016/j.ejmech.2012.01.019. Epub 2012 Jan 24. Eur J Med Chem. 2012. PMID: 22301213

5

Synthesis of novel azo-resveratrol, azo-oxyresveratrol and their derivatives as potent tyrosinase inhibitors.

Song YM, Ha YM, Kim JA, Chung KW, Uehara Y, Lee KJ, Chun P, Byun Y, Chung HY, Moon HR. Song YM, et al. Among authors: kim ja. Bioorg Med Chem Lett. 2012 Dec 15;22(24):7451-5. doi: 10.1016/j.bmcl.2012.10.050. Epub 2012 Oct 17. Bioorg Med Chem Lett. 2012. PMID: 23142612

6

A novel synthesized tyrosinase inhibitor: (E)-2-((2,4-dihydroxyphenyl)diazenyl)phenyl 4-methylbenzenesulfonate as an azo-resveratrol analog.

Bae SJ, Ha YM, Kim JA, Park JY, Ha TK, Park D, Chun P, Park NH, Moon HR, Chung HY. Bae SJ, et al. Among authors: kim ja. Biosci Biotechnol Biochem. 2013;77(1):65-72. doi: 10.1271/bbb.120547. Epub 2013 Jan 7. Biosci Biotechnol Biochem. 2013. PMID: 23291747 Free article.

7

Efficient and practical synthesis of L-hamamelose.

Kim WH, Kang JA, Lee HR, Park AY, Chun P, Lee B, Kim J, Kim JA, Jeong LS, Moon HR. Kim WH, et al. Among authors: kim ja, kim j. Carbohydr Res. 2009 Nov 23;344(17):2317-21. doi: 10.1016/j.carres.2009.09.011. Epub 2009 Sep 18. Carbohydr Res. 2009. PMID: 19818955

8

A novel resveratrol analogue, HS-1793, inhibits hypoxia-induced HIF-1α and VEGF expression, and migration in human prostate cancer cells.

Kim DH, Hossain MA, Kim MY, Kim JA, Yoon JH, Suh HS, Kim GY, Choi YH, Chung HY, Kim ND. Kim DH, et al. Among authors: kim gy, kim nd, kim ja, kim my. Int J Oncol. 2013 Dec;43(6):1915-24. doi: 10.3892/ijo.2013.2116. Epub 2013 Oct 2. Int J Oncol. 2013. PMID: 24100602

9

HS-1793, a resveratrol analogue, induces cell cycle arrest and apoptotic cell death in human breast cancer cells.

Kim JA, Kim DH, Hossain MA, Kim MY, Sung B, Yoon JH, Suh H, Jeong TC, Chung HY, Kim ND. Kim JA, et al. Among authors: kim dh, kim nd, kim my. Int J Oncol. 2014 Feb;44(2):473-80. doi: 10.3892/ijo.2013.2207. Epub 2013 Dec 5. Int J Oncol. 2014. PMID: 24316714

10

HS-1793, a resveratrol analogue, downregulates the expression of hypoxia-induced HIF-1 and VEGF and inhibits tumor growth of human breast cancer cells in a nude mouse xenograft model.

Kim DH, Sung B, Kim JA, Kang YJ, Hwang SY, Hwang NL, Suh H, Choi YH, Im E, Chung HY, Kim ND. Kim DH, et al. Among authors: kim nd, kim ja. Int J Oncol. 2017 Aug;51(2):715-723. doi: 10.3892/ijo.2017.4058. Epub 2017 Jun 27. Int J Oncol. 2017. PMID: 28656256

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