Fang H - Search Results

1

3D-QSAR study on a series of Bcl-2 protein inhibitors using comparative molecular field analysis.

Hou X, Du J, Fang H, Li M. Hou X, et al. Among authors: fang h. Protein Pept Lett. 2011 May;18(5):440-9. doi: 10.2174/092986611794927992. Protein Pept Lett. 2011. PMID: 21171944

2

Pharmacophore-based design, synthesis, biological evaluation, and 3D-QSAR studies of aryl-piperazines as alpha(1)-adrenoceptor antagonists.

Li MY, Fang H, Xia L. Li MY, et al. Among authors: fang h. Bioorg Med Chem Lett. 2005 Jul 1;15(13):3216-9. doi: 10.1016/j.bmcl.2005.05.003. Bioorg Med Chem Lett. 2005. PMID: 15935663

3

Design and synthesis of boronic-acid-labeled thymidine triphosphate for incorporation into DNA.

Lin N, Yan J, Huang Z, Altier C, Li M, Carrasco N, Suyemoto M, Johnston L, Wang S, Wang Q, Fang H, Caton-Williams J, Wang B. Lin N, et al. Among authors: fang h. Nucleic Acids Res. 2007;35(4):1222-9. doi: 10.1093/nar/gkl1091. Epub 2007 Jan 31. Nucleic Acids Res. 2007. PMID: 17267413 Free PMC article.

4

Computational studies of the binding site of alpha1A-adrenoceptor antagonists.

Li M, Fang H, Du L, Xia L, Wang B. Li M, et al. Among authors: fang h. J Mol Model. 2008 Oct;14(10):957-66. doi: 10.1007/s00894-008-0342-8. Epub 2008 Jul 15. J Mol Model. 2008. PMID: 18626669

5

Selecting aptamers for a glycoprotein through the incorporation of the boronic acid moiety.

Li M, Lin N, Huang Z, Du L, Altier C, Fang H, Wang B. Li M, et al. Among authors: fang h. J Am Chem Soc. 2008 Sep 24;130(38):12636-8. doi: 10.1021/ja801510d. Epub 2008 Sep 3. J Am Chem Soc. 2008. PMID: 18763762 Free PMC article.

6

Potential targets and their relevant inhibitors in anti-influenza fields.

Gong J, Fang H, Li M, Liu Y, Yang K, Liu Y, Xu W. Gong J, et al. Among authors: fang h. Curr Med Chem. 2009;16(28):3716-39. doi: 10.2174/092986709789104984. Curr Med Chem. 2009. PMID: 19747144 Review.

7

Design, synthesis and preliminary activity evaluation of novel L-lysine derivatives as aminopeptidase N/CD13 inhibitors.

Wang Q, Xu F, Mou J, Zhang J, Shang L, Luan Y, Yuan Y, Liu Y, Li M, Fang H, Wang B, Xu W. Wang Q, et al. Among authors: fang h. Protein Pept Lett. 2010 Jul;17(7):847-53. doi: 10.2174/092986610791306661. Protein Pept Lett. 2010. PMID: 20156182

8

Design, synthesis and preliminary activity assay of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives as novel Histone deacetylases (HDACs) inhibitors.

Zhang Y, Feng J, Liu C, Zhang L, Jiao J, Fang H, Su L, Zhang X, Zhang J, Li M, Wang B, Xu W. Zhang Y, et al. Among authors: fang h. Bioorg Med Chem. 2010 Mar 1;18(5):1761-72. doi: 10.1016/j.bmc.2010.01.060. Epub 2010 Feb 6. Bioorg Med Chem. 2010. PMID: 20171895

9

Structure, function and inhibition of Bcl-2 family proteins: a new target for anti-tumor agents.

Xiao G, Fang H, Xing C, Xu W. Xiao G, et al. Among authors: fang h. Mini Rev Med Chem. 2009 Dec;9(14):1596-604. doi: 10.2174/138955709791012238. Mini Rev Med Chem. 2009. PMID: 20236080 Review.

10

Homology modeling, molecular dynamic simulation and docking studies of cyclin dependent kinase 1.

Zhang L, Zhu H, Wang Q, Fang H, Xu W, Li M. Zhang L, et al. Among authors: fang h. J Mol Model. 2011 Feb;17(2):219-26. doi: 10.1007/s00894-010-0710-z. Epub 2010 Apr 26. J Mol Model. 2011. PMID: 20419498

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