Park MK - Search Results

1

Synthesis of N,N',N"-trisubstituted thiourea derivatives and their antagonist effect on the vanilloid receptor.

Park HG, Park MK, Choi JY, Choi SH, Lee J, Park BS, Kim MG, Suh YG, Cho H, Oh U, Lee J, Kim HD, Park YH, Koh HJ, Lim KM, Moh JH, Jew SS. Park HG, et al. Among authors: park bs, park yh, park mk. Bioorg Med Chem Lett. 2003 Feb 24;13(4):601-4. doi: 10.1016/s0960-894x(02)01040-5. Bioorg Med Chem Lett. 2003. PMID: 12639539

2

N-4-Substituted-benzyl-N'-tert-butylbenzyl thioureas as vanilloid receptor ligands: investigation on the role of methanesulfonamido group in antagonistic activity.

Park HG, Choi JY, Choi SH, Park MK, Lee J, Suh YG, Cho H, Oh U, Lee J, Kang SU, Lee J, Kim HD, Park YH, Su Jeong Y, Kyu Choi J, Jew SS. Park HG, et al. Among authors: park yh, park mk. Bioorg Med Chem Lett. 2004 Feb 9;14(3):787-91. doi: 10.1016/j.bmcl.2003.11.019. Bioorg Med Chem Lett. 2004. PMID: 14741290

3

N-4-methansulfonamidobenzyl-N'-2-substituted-4-tert-butyl-benzyl thioureas as potent vanilloid receptor antagonistic ligands.

Park HG, Choi JY, Choi SH, Park MK, Lee J, Suh YG, Cho H, Oh U, Kim HD, Joo YH, Kim SY, Park YH, Jeong YS, Choi JK, Kim JK, Jew SS. Park HG, et al. Among authors: park yh, park mk. Bioorg Med Chem Lett. 2004 Apr 5;14(7):1693-6. doi: 10.1016/j.bmcl.2004.01.041. Bioorg Med Chem Lett. 2004. PMID: 15026052

4

Biarylcarboxybenzamide derivatives as potent vanilloid receptor (VR1) antagonistic ligands.

Park HG, Choi JY, Kim MH, Choi SH, Park MK, Lee J, Suh YG, Cho H, Oh U, Kim HD, Joo YH, Shin SS, Kim JK, Jeong YS, Koh HJ, Park YH, Jew SS. Park HG, et al. Among authors: park yh, park mk. Bioorg Med Chem Lett. 2005 Feb 1;15(3):631-4. doi: 10.1016/j.bmcl.2004.11.033. Bioorg Med Chem Lett. 2005. PMID: 15664827

5

Synthesis of 2-substituted-pyrrolidinethiourea derivatives and their antagonist effect on vanilloid receptor.

Park Hg, Park Mk, Choi Jy, Choi Sh, Lee J, Suh Yg, Oh U, Lee J, Kim HD, Park YH, Jeong YS, Choi JK, Jew Ss. Park Hg, et al. Among authors: park yh, park mk. Bioorg Med Chem Lett. 2003 Jan 20;13(2):197-200. doi: 10.1016/s0960-894x(02)00887-9. Bioorg Med Chem Lett. 2003. PMID: 12482422

6

Highly enantioselective phase-transfer catalytic alkylation in the preparation of non-natural alpha-amino acids via solid phase synthesis using aldimine linker.

Park HG, Kim MJ, Park MK, Jung HJ, Lee J, Choi SH, Lee YJ, Jeong BS, Lee JH, Yoo MS, Ku JM, Jew SS. Park HG, et al. Among authors: park mk. J Org Chem. 2005 Mar 4;70(5):1904-6. doi: 10.1021/jo0481957. J Org Chem. 2005. PMID: 15730319

7

A novel class of inhibitors for steroid 5alpha-reductase: synthesis and evaluation of umbelliferone derivatives.

Fan G, Mar W, Park MK, Choi EW, Kim K, Kim S. Fan G, et al. Among authors: park mk. Bioorg Med Chem Lett. 2001 Sep 3;11(17):2361-3. doi: 10.1016/s0960-894x(01)00429-2. Bioorg Med Chem Lett. 2001. PMID: 11527731

8

Design, synthesis, and biological evaluation of novel pyrrolo[1,2-a]pyrazine derivatives.

Kim J, Park M, Choi J, Singh DK, Kwon HJ, Kim SH, Kim I. Kim J, et al. Bioorg Med Chem Lett. 2019 Jun 1;29(11):1350-1356. doi: 10.1016/j.bmcl.2019.03.044. Epub 2019 Mar 28. Bioorg Med Chem Lett. 2019. PMID: 30954427

9

A novel class of highly potent multidrug resistance reversal agents: disubstituted adamantyl derivatives.

Min KH, Xia Y, Kim EK, Jin Y, Kaur N, Kim ES, Kim DK, Jung HY, Choi Y, Park MK, Min YK, Lee K, Lee K. Min KH, et al. Among authors: park mk. Bioorg Med Chem Lett. 2009 Sep 15;19(18):5376-9. doi: 10.1016/j.bmcl.2009.07.127. Epub 2009 Aug 6. Bioorg Med Chem Lett. 2009. PMID: 19679475

10

Novel inhibitory effects of cardamonin on thromboxane A2-induced scratching response: Blocking of Gh/transglutaminase-2 binding to thromboxane A2 receptor.

Park MK, Choi JK, Kim HJ, Nakahata N, Lim KM, Kim SY, Lee CH. Park MK, et al. Pharmacol Biochem Behav. 2014 Nov;126:131-5. doi: 10.1016/j.pbb.2014.09.011. Epub 2014 Oct 5. Pharmacol Biochem Behav. 2014. PMID: 25285619

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