Fang H - Search Results

1

Protein Flexibility in Docking-Based Virtual Screening: Discovery of Novel Lymphoid-Specific Tyrosine Phosphatase Inhibitors Using Multiple Crystal Structures.

Hou X, Li K, Yu X, Sun JP, Fang H. Hou X, et al. Among authors: fang h. J Chem Inf Model. 2015 Sep 28;55(9):1973-83. doi: 10.1021/acs.jcim.5b00344. Epub 2015 Sep 17. J Chem Inf Model. 2015. PMID: 26360643

2

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

3

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

4

Design, synthesis and preliminary bioactivity studies of 1,3,4-thiadiazole hydroxamic acid derivatives as novel histone deacetylase inhibitors.

Guan P, Sun F, Hou X, Wang F, Yi F, Xu W, Fang H. Guan P, et al. Among authors: fang h. Bioorg Med Chem. 2012 Jun 15;20(12):3865-72. doi: 10.1016/j.bmc.2012.04.032. Epub 2012 Apr 21. Bioorg Med Chem. 2012. PMID: 22579621

5

Density functional theory based quantitative structure-property relationship studies on coumarin-based prodrugs.

Yang X, Hou X, Wang B, Li M, Fang H. Yang X, et al. Among authors: fang h. Biosci Trends. 2012 Oct;6(5):234-40. doi: 10.5582/bst.2012.v6.5.234. Biosci Trends. 2012. PMID: 23229116 Free article.

6

How to improve docking accuracy of AutoDock4.2: a case study using different electrostatic potentials.

Hou X, Du J, Zhang J, Du L, Fang H, Li M. Hou X, et al. Among authors: fang h. J Chem Inf Model. 2013 Jan 28;53(1):188-200. doi: 10.1021/ci300417y. Epub 2013 Jan 2. J Chem Inf Model. 2013. PMID: 23244516

7

Cadmium is a potent inhibitor of PPM phosphatases and targets the M1 binding site.

Pan C, Liu HD, Gong Z, Yu X, Hou XB, Xie DD, Zhu XB, Li HW, Tang JY, Xu YF, Yu JQ, Zhang LY, Fang H, Xiao KH, Chen YG, Wang JY, Pang Q, Chen W, Sun JP. Pan C, et al. Among authors: fang h. Sci Rep. 2013;3:2333. doi: 10.1038/srep02333. Sci Rep. 2013. PMID: 23903585 Free PMC article.

8

Design, synthesis and preliminary bioactivity studies of 1,2-dihydrobenzo[d]isothiazol-3-one-1,1-dioxide hydroxamic acid derivatives as novel histone deacetylase inhibitors.

Han L, Wang L, Hou X, Fu H, Song W, Tang W, Fang H. Han L, et al. Among authors: fang h. Bioorg Med Chem. 2014 Mar 1;22(5):1529-38. doi: 10.1016/j.bmc.2014.01.045. Epub 2014 Feb 1. Bioorg Med Chem. 2014. PMID: 24525003

9

High-performance liquid chromatographic enantioseparation of 3,5-disubstituted hydantoins analogs and temperature-induced reversals of elution orders on a polysaccharide-based chiral stationary phase.

Yang X, Su L, Hou X, Ding S, Xu W, Wang B, Fang H. Yang X, et al. Among authors: fang h. J Chromatogr A. 2014 Aug 15;1355:291-5. doi: 10.1016/j.chroma.2014.06.022. Epub 2014 Jun 12. J Chromatogr A. 2014. PMID: 24973033

10

Antagonists of IAP proteins: novel anti-tumor agents.

Wan Y, Liu T, Hou X, Dun Y, Guan P, Fang H. Wan Y, et al. Among authors: fang h. Curr Med Chem. 2014;21(34):3877-92. doi: 10.2174/0929867321666140826115258. Curr Med Chem. 2014. PMID: 25174926 Review.

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