Chang C - Search Results

1

Facile identification of dual FLT3-Aurora A inhibitors: a computer-guided drug design approach.

Chang Hsu Y, Ke YY, Shiao HY, Lee CC, Lin WH, Chen CH, Yen KJ, Hsu JT, Chang C, Hsieh HP. Chang Hsu Y, et al. Among authors: chang c. ChemMedChem. 2014 May;9(5):953-61. doi: 10.1002/cmdc.201300571. Epub 2014 Mar 24. ChemMedChem. 2014. PMID: 24665000

2

Ligand efficiency based approach for efficient virtual screening of compound libraries.

Ke YY, Coumar MS, Shiao HY, Wang WC, Chen CW, Song JS, Chen CH, Lin WH, Wu SH, Hsu JT, Chang CM, Hsieh HP. Ke YY, et al. Eur J Med Chem. 2014 Aug 18;83:226-35. doi: 10.1016/j.ejmech.2014.06.029. Epub 2014 Jun 14. Eur J Med Chem. 2014. PMID: 24960626

3

Synthesis and structure-activity relationship of 2-aminobenzophenone derivatives as antimitotic agents.

Liou JP, Chang CW, Song JS, Yang YN, Yeh CF, Tseng HY, Lo YK, Chang YL, Chang CM, Hsieh HP. Liou JP, et al. J Med Chem. 2002 Jun 6;45(12):2556-62. doi: 10.1021/jm010365+. J Med Chem. 2002. PMID: 12036364

4

Synthesis and biological activities of 2-amino-1-arylidenamino imidazoles as orally active anticancer agents.

Li WT, Hwang DR, Song JS, Chen CP, Chuu JJ, Hu CB, Lin HL, Huang CL, Huang CY, Tseng HY, Lin CC, Chen TW, Lin CH, Wang HS, Shen CC, Chang CM, Chao YS, Chen CT. Li WT, et al. J Med Chem. 2010 Mar 25;53(6):2409-17. doi: 10.1021/jm901501s. J Med Chem. 2010. PMID: 20170097

5

Synthesis and biological evaluation of 2-amino-1-thiazolyl imidazoles as orally active anticancer agents.

Li WT, Hwang DR, Song JS, Chen CP, Chen TW, Lin CH, Chuu JJ, Lien TW, Hsu TA, Huang CL, Tseng HY, Lin CC, Lin HL, Chang CM, Chao YS, Chen CT. Li WT, et al. Invest New Drugs. 2012 Feb;30(1):164-75. doi: 10.1007/s10637-010-9547-7. Epub 2010 Oct 2. Invest New Drugs. 2012. PMID: 20890633

6

Design, synthesis, and structure-activity relationship of pyridyl imidazolidinones: a novel class of potent and selective human enterovirus 71 inhibitors.

Shia KS, Li WT, Chang CM, Hsu MC, Chern JH, Leong MK, Tseng SN, Lee CC, Lee YC, Chen SJ, Peng KC, Tseng HY, Chang YL, Tai CL, Shih SR. Shia KS, et al. J Med Chem. 2002 Apr 11;45(8):1644-55. doi: 10.1021/jm010536a. J Med Chem. 2002. PMID: 11931618

7

Synthesis and in vitro cytotoxicity of 5-substituted 2-cyanoimino-4-imidazodinone and 2-cyanoimino-4-pyrimidinone derivatives.

Chern JH, Shia KS, Chang CM, Lee CC, Lee YC, Tai CL, Lin YT, Chang CS, Tseng HY. Chern JH, et al. Bioorg Med Chem Lett. 2004 Mar 8;14(5):1169-72. doi: 10.1016/j.bmcl.2003.12.073. Bioorg Med Chem Lett. 2004. PMID: 14980658

8

Antitumor activities and pharmacokinetics of silatecans DB-67 and DB-91.

Yeh TK, Li CM, Chen CP, Chuu JJ, Huang CL, Wang HS, Shen CC, Lee TY, Chang CY, Chang CM, Chao YS, Lin CT, Chang JY, Chen CT. Yeh TK, et al. Pharmacol Res. 2010 Feb;61(2):108-15. doi: 10.1016/j.phrs.2009.07.005. Epub 2009 Jul 28. Pharmacol Res. 2010. PMID: 19643180

9

A novel dengue virus inhibitor, BP13944, discovered by high-throughput screening with dengue virus replicon cells selects for resistance in the viral NS2B/NS3 protease.

Yang CC, Hu HS, Wu RH, Wu SH, Lee SJ, Jiaang WT, Chern JH, Huang ZS, Wu HN, Chang CM, Yueh A. Yang CC, et al. Antimicrob Agents Chemother. 2014;58(1):110-9. doi: 10.1128/AAC.01281-13. Epub 2013 Oct 21. Antimicrob Agents Chemother. 2014. PMID: 24145533 Free PMC article.

10

A novel approach to propagate flavivirus infectious cDNA clones in bacteria by introducing tandem repeat sequences upstream of virus genome.

Pu SY, Wu RH, Tsai MH, Yang CC, Chang CM, Yueh A. Pu SY, et al. J Gen Virol. 2014 Jul;95(Pt 7):1493-1503. doi: 10.1099/vir.0.064915-0. Epub 2014 Apr 11. J Gen Virol. 2014. PMID: 24728712

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