Shia KS - Search Results

1

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

2

Design, synthesis, and biological evaluation of a cephalosporin-monohydroguaiaretic acid prodrug activated by a monoclonal antibody-beta-lactamase conjugate.

Hakimelahi GH, Shia KS, Pasdar M, Hakimelahi S, Khalafi-Nezhad A, Soltani MN, Mei NW, Mei HC, Saboury AA, Rezaei-Tavirani M, Moosavi-Movahedi AA. Hakimelahi GH, et al. Among authors: shia ks. Bioorg Med Chem. 2002 Sep;10(9):2927-32. doi: 10.1016/s0968-0896(02)00140-2. Bioorg Med Chem. 2002. PMID: 12110314

3

Design, synthesis, and biological evaluation of a series of beta-lactam-based prodrugs.

Hakimelahi GH, Shia KS, Xue C, Hakimelahi S, Moosavi-Movahedi AA, Saboury AA, Khalafi-Nezhad A, Soltani-Rad MN, Osyetrov V, Wang K, Liao JH, Luo FT. Hakimelahi GH, et al. Among authors: shia ks. Bioorg Med Chem. 2002 Nov;10(11):3489-98. doi: 10.1016/s0968-0896(02)00256-0. Bioorg Med Chem. 2002. PMID: 12213463

4

Synthesis and anticancer evaluation of vitamin K(3) analogues.

Chen C, Liu YZ, Shia KS, Tseng HY. Chen C, et al. Among authors: shia ks. Bioorg Med Chem Lett. 2002 Oct 7;12(19):2729-32. doi: 10.1016/s0960-894x(02)00532-2. Bioorg Med Chem Lett. 2002. PMID: 12217364

5

Application of the Barton photochemical reaction in the synthesis of 1-dethia-3-aza-1-carba-2-oxacephem: a novel agent against resistant pathogenic microorganisms.

Hakimelahi GH, Li PC, Moosavi-Movahedi AA, Chamani J, Khodarahmi GA, Ly TW, Valiyev F, Leong MK, Hakimelahi S, Shia KS, Chao I. Hakimelahi GH, et al. Among authors: shia ks. Org Biomol Chem. 2003 Jul 21;1(14):2461-7. doi: 10.1039/b304167k. Org Biomol Chem. 2003. PMID: 12956062

6

Design, synthesis, and anticancer activity of phosphonic acid diphosphate derivative of adenine-containing butenolide and its water-soluble derivatives of paclitaxel with high antitumor activity.

Moosavi-Movahedi AA, Hakimelahi S, Chamani J, Khodarahmi GA, Hassanzadeh F, Luo FT, Ly TW, Shia KS, Yen CF, Jain ML, Kulatheeswaran R, Xue C, Pasdar M, Hakimelahi GH. Moosavi-Movahedi AA, et al. Among authors: shia ks. Bioorg Med Chem. 2003 Oct 1;11(20):4303-13. doi: 10.1016/s0968-0896(03)00524-8. Bioorg Med Chem. 2003. PMID: 13129566

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. Among authors: shia ks. 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

Design, synthesis, and structure-activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors.

Chern JH, Shia KS, Hsu TA, Tai CL, Lee CC, Lee YC, Chang CS, Tseng SN, Shih SR. Chern JH, et al. Among authors: shia ks. Bioorg Med Chem Lett. 2004 May 17;14(10):2519-25. doi: 10.1016/j.bmcl.2004.02.092. Bioorg Med Chem Lett. 2004. PMID: 15109643

9

Selective human enterovirus and rhinovirus inhibitors: An overview of capsid-binding and protease-inhibiting molecules.

Shih SR, Chen SJ, Hakimelahi GH, Liu HJ, Tseng CT, Shia KS. Shih SR, et al. Among authors: shia ks. Med Res Rev. 2004 Jul;24(4):449-74. doi: 10.1002/med.10067. Med Res Rev. 2004. PMID: 15170592 Free PMC article. Review.

10

Mutation in enterovirus 71 capsid protein VP1 confers resistance to the inhibitory effects of pyridyl imidazolidinone.

Shih SR, Tsai MC, Tseng SN, Won KF, Shia KS, Li WT, Chern JH, Chen GW, Lee CC, Lee YC, Peng KC, Chao YS. Shih SR, et al. Among authors: shia ks. Antimicrob Agents Chemother. 2004 Sep;48(9):3523-9. doi: 10.1128/AAC.48.9.3523-3529.2004. Antimicrob Agents Chemother. 2004. PMID: 15328120 Free PMC article.

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