Park CH - Search Results

1

The design, synthesis and physical chemical properties of novel human vasopressin V2-receptor antagonists optimized for parenteral delivery.

Ashwell MA, Bagli JF, Caggiano TJ, Chan PS, Molinari AJ, Palka C, Park CH, Rogers JF, Sherman M, Trybulski EJ, Williams DK. Ashwell MA, et al. Among authors: park ch. Bioorg Med Chem Lett. 2000 Apr 17;10(8):783-6. doi: 10.1016/s0960-894x(00)00095-0. Bioorg Med Chem Lett. 2000. PMID: 10782686

2

Pyridobenzodiazepines: a novel class of orally active, vasopressin V2 receptor selective agonists.

Failli AA, Shumsky JS, Steffan RJ, Caggiano TJ, Williams DK, Trybulski EJ, Ning X, Lock Y, Tanikella T, Hartmann D, Chan PS, Park CH. Failli AA, et al. Among authors: park ch. Bioorg Med Chem Lett. 2006 Feb 15;16(4):954-9. doi: 10.1016/j.bmcl.2005.10.107. Epub 2005 Nov 15. Bioorg Med Chem Lett. 2006. PMID: 16297621

3

Metabolites of the angiotensin II antagonist tasosartan: the importance of a second acidic group.

Ellingboe JW, Collini MD, Quagliato D, Chen J, Antane M, Schmid J, Hartupee D, White V, Park CH, Tanikella T, Bagli JF. Ellingboe JW, et al. Among authors: park ch. J Med Chem. 1998 Oct 22;41(22):4251-60. doi: 10.1021/jm970690q. J Med Chem. 1998. PMID: 9784100

4

Pyrido[2,3-d]pyrimidine angiotensin II antagonists.

Ellingboe JW, Antane M, Nguyen TT, Collini MD, Antane S, Bender R, Hartupee D, White V, McCallum J, Park CH, et al. Ellingboe JW, et al. Among authors: park ch. J Med Chem. 1994 Feb 18;37(4):542-50. doi: 10.1021/jm00030a013. J Med Chem. 1994. PMID: 8120871

5

Chromen-based TNF-alpha converting enzyme (TACE) inhibitors: design, synthesis, and biological evaluation.

Chun K, Park SK, Kim HM, Choi Y, Kim MH, Park CH, Joe BY, Chun TG, Choi HM, Lee HY, Hong SH, Kim MS, Nam KY, Han G. Chun K, et al. Among authors: park sk, park ch. Bioorg Med Chem. 2008 Jan 1;16(1):530-5. doi: 10.1016/j.bmc.2007.09.014. Epub 2007 Sep 14. Bioorg Med Chem. 2008. PMID: 17936631

6

Antibacterials. synthesis and structure-activity studies of 3-aryl-2-oxooxazolidines. 4. Multiply-substituted aryl derivatives.

Park CH, Brittelli DR, Wang CL, Marsh FD, Gregory WA, Wuonola MA, McRipley RJ, Eberly VS, Slee AM, Forbes M. Park CH, et al. J Med Chem. 1992 Mar 20;35(6):1156-65. doi: 10.1021/jm00084a022. J Med Chem. 1992. PMID: 1552508

7

Synthesis and evaluation of tricyclic derivatives containing a non-aromatic amide as inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1).

Park CH, Chun K, Joe BY, Park JS, Kim YC, Choi JS, Ryu DK, Koh SH, Cho GW, Kim SH, Kim MH. Park CH, et al. Among authors: park js. Bioorg Med Chem Lett. 2010 Apr 1;20(7):2250-3. doi: 10.1016/j.bmcl.2010.02.014. Epub 2010 Feb 8. Bioorg Med Chem Lett. 2010. PMID: 20189385

8

Antibacterials. Synthesis and structure-activity studies of 3-aryl-2-oxooxazolidines. 2. The "A" group.

Gregory WA, Brittelli DR, Wang CL, Kezar HS 3rd, Carlson RK, Park CH, Corless PF, Miller SJ, Rajagopalan P, Wuonola MA, et al. Gregory WA, et al. Among authors: park ch. J Med Chem. 1990 Sep;33(9):2569-78. doi: 10.1021/jm00171a035. J Med Chem. 1990. PMID: 2118186

9

Structure based optimization of chromen-based TNF-α converting enzyme (TACE) inhibitors on S1' pocket and their quantitative structure-activity relationship (QSAR) study.

Yang JS, Chun K, Park JE, Cho M, Seo J, Song D, Yoon H, Park CH, Joe BY, Choi JH, Kim MH, Han G. Yang JS, et al. Among authors: park je, park ch. Bioorg Med Chem. 2010 Dec 15;18(24):8618-29. doi: 10.1016/j.bmc.2010.10.006. Bioorg Med Chem. 2010. PMID: 21078557

10

Discovery of thienopyrimidine-based FLT3 inhibitors from the structural modification of known IKKβ inhibitors.

Park CH, Lee C, Yang JS, Joe BY, Chun K, Kim H, Kim HY, Kang JS, Lee JI, Kim MH, Han G. Park CH, et al. Bioorg Med Chem Lett. 2014 Jun 15;24(12):2655-60. doi: 10.1016/j.bmcl.2014.04.058. Epub 2014 Apr 24. Bioorg Med Chem Lett. 2014. PMID: 24813730

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