Feng H - Search Results

1

Total synthesis of novel D-ring-modified triptolide analogues: structure-cytotoxic activity relationship studies on the D-ring of triptolide.

Zhou B, Li X, Tang H, Miao Z, Feng H, Li Y. Zhou B, et al. Among authors: feng h. Org Biomol Chem. 2011 May 7;9(9):3176-9. doi: 10.1039/c0ob01239d. Epub 2011 Mar 15. Org Biomol Chem. 2011. PMID: 21409265

2

Design and synthesis of novel C14-hydroxyl substituted triptolide derivatives as potential selective antitumor agents.

Li Z, Zhou ZL, Miao ZH, Lin LP, Feng HJ, Tong LJ, Ding J, Li YC. Li Z, et al. J Med Chem. 2009 Aug 27;52(16):5115-23. doi: 10.1021/jm900342g. J Med Chem. 2009. PMID: 19637874

3

Synthesis and biological evaluation of novel triptolide analogues for anticancer activity.

Zhou B, Miao Z, Deng G, Ding J, Yang Y, Feng H, Li Y. Zhou B, et al. Among authors: feng h. Bioorg Med Chem Lett. 2010 Nov 1;20(21):6217-21. doi: 10.1016/j.bmcl.2010.08.106. Epub 2010 Aug 26. Bioorg Med Chem Lett. 2010. PMID: 20833543

4

Design, synthesis and structure-activity relationships studies on the D ring of the natural product triptolide.

Xu H, Tang H, Feng H, Li Y. Xu H, et al. Among authors: feng h. ChemMedChem. 2014 Feb;9(2):290-5. doi: 10.1002/cmdc.201300409. Epub 2013 Dec 11. ChemMedChem. 2014. PMID: 24339424

5

Design, synthesis and anticancer activity evaluation of novel C14 heterocycle substituted epi-triptolide.

Xu H, Tang H, Feng H, Li Y. Xu H, et al. Among authors: feng h. Eur J Med Chem. 2014 Feb 12;73:46-55. doi: 10.1016/j.ejmech.2013.11.044. Epub 2013 Dec 14. Eur J Med Chem. 2014. PMID: 24378709

6

Divergent total synthesis of triptolide, triptonide, tripdiolide, 16-hydroxytriptolide, and their analogues.

Xu H, Tang H, Feng H, Li Y. Xu H, et al. Among authors: feng h. J Org Chem. 2014 Nov 7;79(21):10110-22. doi: 10.1021/jo501744j. Epub 2014 Oct 24. J Org Chem. 2014. PMID: 25296383

7

Semisynthesis of triptolide analogues: effect of B-ring substituents on cytotoxic activities.

Xu H, Chen Y, Tang H, Feng H, Li Y. Xu H, et al. Among authors: feng h. Bioorg Med Chem Lett. 2014 Dec 15;24(24):5671-5674. doi: 10.1016/j.bmcl.2014.10.069. Epub 2014 Oct 29. Bioorg Med Chem Lett. 2014. PMID: 25467158

8

Access to Six- and Seven-Membered 1,7-Fused Indolines via Rh(III)-Catalyzed Redox-Neutral C7-Selective C-H Functionalization of Indolines with Alkynes and Alkenes.

Wang X, Tang H, Feng H, Li Y, Yang Y, Zhou B. Wang X, et al. Among authors: feng h. J Org Chem. 2015 Jun 19;80(12):6238-49. doi: 10.1021/acs.joc.5b00684. Epub 2015 Jun 1. J Org Chem. 2015. PMID: 25989195

9

[Vitro antitumor activity and synthesis of the key intermediate of bakuchiol].

Chen HL, Feng HJ, Li YC. Chen HL, et al. Yao Xue Xue Bao. 2010 Apr;45(4):467-70. Yao Xue Xue Bao. 2010. PMID: 21355211 Chinese.

10

Synthesis and structure-immunosuppressive activity relationships of bakuchiol and its derivatives.

Chen H, Du X, Tang W, Zhou Y, Zuo J, Feng H, Li Y. Chen H, et al. Among authors: feng h. Bioorg Med Chem. 2008 Mar 1;16(5):2403-11. doi: 10.1016/j.bmc.2007.11.054. Epub 2007 Nov 28. Bioorg Med Chem. 2008. PMID: 18063371

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