Fang H - Search Results

1

Design, synthesis and biological evaluation of 3-aryl-rhodanine benzoic acids as anti-apoptotic protein Bcl-2 inhibitors.

Fu H, Hou X, Wang L, Dun Y, Yang X, Fang H. Fu H, et al. Among authors: fang h. Bioorg Med Chem Lett. 2015 Nov 15;25(22):5265-9. doi: 10.1016/j.bmcl.2015.09.051. Epub 2015 Sep 25. Bioorg Med Chem Lett. 2015. PMID: 26421995

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, synthesis and preliminary evaluation of new cinnamoyl pyrrolidine derivatives as potent gelatinase inhibitors.

Zhang L, Zhang J, Fang H, Wang Q, Xu W. Zhang L, et al. Among authors: fang h. Bioorg Med Chem. 2006 Dec 15;14(24):8286-94. doi: 10.1016/j.bmc.2006.09.015. Epub 2006 Sep 27. Bioorg Med Chem. 2006. PMID: 17008101

4

Design, synthesis, inhibitory activity, and SAR studies of pyrrolidine derivatives as neuraminidase inhibitors.

Zhang J, Wang Q, Fang H, Xu W, Liu A, Du G. Zhang J, et al. Among authors: fang h. Bioorg Med Chem. 2007 Apr 1;15(7):2749-58. doi: 10.1016/j.bmc.2007.01.020. Epub 2007 Jan 19. Bioorg Med Chem. 2007. PMID: 17287121

5

Novel 3-galloylamido-N'-substituted-2,6-piperidinedione-N-acetamide peptidomimetics as metalloproteinase inhibitors.

Li Q, Fang H, Xu W. Li Q, et al. Among authors: fang h. Bioorg Med Chem Lett. 2007 May 15;17(10):2935-8. doi: 10.1016/j.bmcl.2006.12.095. Epub 2007 Jan 5. Bioorg Med Chem Lett. 2007. PMID: 17433673

6

Design, synthesis, and preliminary evaluation of 4-(6-(3-nitroguanidino)hexanamido)pyrrolidine derivatives as potential iNOS inhibitors.

Liu FZ, Fang H, Zhu HW, Wang Q, Yang Y, Xu WF. Liu FZ, et al. Among authors: fang h. Bioorg Med Chem. 2008 Jan 1;16(1):578-85. doi: 10.1016/j.bmc.2007.04.030. Epub 2007 Apr 25. Bioorg Med Chem. 2008. PMID: 17937988

7

Design, synthesis, inhibitory activity, and SAR studies of hydrophobic p-aminosalicylic acid derivatives as neuraminidase inhibitors.

Zhang J, Wang Q, Fang H, Xu W, Liu A, Du G. Zhang J, et al. Among authors: fang h. Bioorg Med Chem. 2008 Apr 1;16(7):3839-47. doi: 10.1016/j.bmc.2008.01.036. Epub 2008 Jan 30. Bioorg Med Chem. 2008. PMID: 18304821

8

Design, synthesis and preliminary evaluation of novel pyrrolidine derivatives as matrix metalloproteinase inhibitors.

Cheng XC, Wang Q, Fang H, Tang W, Xu WF. Cheng XC, et al. Among authors: fang h. Eur J Med Chem. 2008 Oct;43(10):2130-9. doi: 10.1016/j.ejmech.2007.12.020. Epub 2007 Dec 31. Eur J Med Chem. 2008. PMID: 18362041

9

Design, synthesis and evaluation of novel sulfonyl pyrrolidine derivatives as matrix metalloproteinase inhibitors.

Cheng XC, Wang Q, Fang H, Tang W, Xu WF. Cheng XC, et al. Among authors: fang h. Bioorg Med Chem. 2008 May 15;16(10):5398-404. doi: 10.1016/j.bmc.2008.04.027. Epub 2008 Apr 15. Bioorg Med Chem. 2008. PMID: 18440232

10

Design, synthesis, and QSAR studies of novel lysine derives as amino-peptidase N/CD13 inhibitors.

Wang Q, Chen M, Zhu H, Zhang J, Fang H, Wang B, Xu W. Wang Q, et al. Among authors: fang h. Bioorg Med Chem. 2008 May 15;16(10):5473-81. doi: 10.1016/j.bmc.2008.04.012. Epub 2008 Apr 11. Bioorg Med Chem. 2008. PMID: 18467109

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