Park Choo HY - Search Results

1

Preparation of piperazine derivatives as 5-HT7 receptor antagonists.

Yoon J, Yoo EA, Kim JY, Pae AN, Rhim H, Park WK, Kong JY, Park Choo HY. Yoon J, et al. Among authors: park choo hy, park wk. Bioorg Med Chem. 2008 May 15;16(10):5405-12. doi: 10.1016/j.bmc.2008.04.023. Epub 2008 Apr 15. Bioorg Med Chem. 2008. PMID: 18456500

2

Synthesis and biological evaluation of (phenylpiperazinyl-propyl)arylsulfonamides as selective 5-HT(2A) receptor antagonists.

Yoo E, Yoon J, Pae AN, Rhim H, Park WK, Kong JY, Park Choo HY. Yoo E, et al. Among authors: park choo hy, park wk. Bioorg Med Chem. 2010 Feb 15;18(4):1665-75. doi: 10.1016/j.bmc.2009.12.067. Epub 2010 Jan 4. Bioorg Med Chem. 2010. PMID: 20096593

3

Synthesis and biological evaluation of benzoisothiazole derivatives possessing N,N-dimethylformimidamide group as 5-HT₆ receptor antagonists.

Yoo E, Hayat F, Rhim H, Park Choo HY. Yoo E, et al. Among authors: park choo hy. Bioorg Med Chem. 2012 Apr 15;20(8):2707-12. doi: 10.1016/j.bmc.2012.02.020. Epub 2012 Feb 16. Bioorg Med Chem. 2012. PMID: 22405919

4

3-Benzamides and 3,4,5-trimethoxyphenyl amines as calcium channel blockers.

Kang B, Oh JA, Lee JY, Rhim H, Yune TY, Park Choo HY. Kang B, et al. Among authors: park choo hy. Bioorg Med Chem. 2015 Sep 15;23(18):6166-72. doi: 10.1016/j.bmc.2015.07.067. Epub 2015 Aug 1. Bioorg Med Chem. 2015. PMID: 26296911

5

Synthesis of 1-/2-substituted-[1,2,3]triazolo[4,5-g]phthalazine-4,9-diones and evaluation of their cytotoxicity and topoisomerase II inhibition.

Kim JS, Rhee HK, Park HJ, Lee SK, Lee CO, Park Choo HY. Kim JS, et al. Among authors: park choo hy, park hj. Bioorg Med Chem. 2008 Apr 15;16(8):4545-50. doi: 10.1016/j.bmc.2008.02.049. Epub 2008 Feb 19. Bioorg Med Chem. 2008. PMID: 18321715

6

The development of 3D-QSAR study and recursive partitioning of heterocyclic quinone derivatives with antifungal activity.

Choi SY, Shin JH, Ryu CK, Nam KY, No KT, Park Choo HY. Choi SY, et al. Among authors: park choo hy. Bioorg Med Chem. 2006 Mar 1;14(5):1608-17. doi: 10.1016/j.bmc.2005.10.010. Epub 2005 Nov 2. Bioorg Med Chem. 2006. PMID: 16263301

7

Synthesis and cytotoxicity evaluation of substituted pyridazino[4,5-b]phenazine-5,12-diones and tri/tetra-azabenzofluorene-5,6-diones.

Lee HJ, Kim JS, Suh ME, Park HJ, Lee SK, Rhee HK, Kim HJ, Seo EK, Kim C, Lee CO, Park Choo HY. Lee HJ, et al. Among authors: park choo hy, park hj. Eur J Med Chem. 2007 Feb;42(2):168-74. doi: 10.1016/j.ejmech.2006.09.007. Epub 2006 Oct 27. Eur J Med Chem. 2007. PMID: 17070967

8

Synthesis, biological evaluation, and molecular docking study of 3-(3'-heteroatom substituted-2'-hydroxy-1'-propyloxy) xanthone analogues as novel topoisomerase IIα catalytic inhibitor.

Jun KY, Lee EY, Jung MJ, Lee OH, Lee ES, Park Choo HY, Na Y, Kwon Y. Jun KY, et al. Among authors: park choo hy. Eur J Med Chem. 2011 Jun;46(6):1964-71. doi: 10.1016/j.ejmech.2011.01.011. Epub 2011 Jan 15. Eur J Med Chem. 2011. PMID: 21419530

9

5-Lipoxygenase inhibitors suppress RANKL-induced osteoclast formation via NFATc1 expression.

Kang JH, Ting Z, Moon MR, Sim JS, Lee JM, Doh KE, Hong S, Cui M, Choi S, Chang HW, Park Choo HY, Yim M. Kang JH, et al. Among authors: park choo hy. Bioorg Med Chem. 2015 Nov 1;23(21):7069-78. doi: 10.1016/j.bmc.2015.09.025. Epub 2015 Sep 15. Bioorg Med Chem. 2015. PMID: 26432605

10

A comparative study of quantitative structure activity relationship methods based on antitumor diarylsulfonylureas.

Park Choo HY, Lim JS, Kam Y, Kim SY, Lee J. Park Choo HY, et al. Eur J Med Chem. 2001 Oct;36(10):829-36. doi: 10.1016/s0223-5234(01)01276-4. Eur J Med Chem. 2001. PMID: 11738489

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