Hu L - Search Results

1

Synthesis and structure-activity relationships study of novel anti-tumor carbamate anhydrovinblastine analogues.

Shao Y, Ding H, Tang W, Lou L, Hu L. Shao Y, et al. Among authors: hu l. Bioorg Med Chem. 2007 Aug 1;15(15):5061-75. doi: 10.1016/j.bmc.2007.05.045. Epub 2007 May 23. Bioorg Med Chem. 2007. PMID: 17544278

2

Synthesis and structure-activity relationship studies of cytotoxic anhydrovinblastine amide derivatives.

Shao Y, Zhang HK, Ding H, Quan HT, Lou LG, Hu LH. Shao Y, et al. J Nat Prod. 2009 Jun;72(6):1170-7. doi: 10.1021/np900157t. J Nat Prod. 2009. PMID: 19499938

3

Synthesis and structure-activity relationship studies of cytotoxic ester and ether anhydrovinblastine derivatives.

Zhang HK, Shao Y, Ding H, Hu LH. Zhang HK, et al. J Nat Prod. 2008 Oct;71(10):1669-76. doi: 10.1021/np800284h. Epub 2008 Sep 4. J Nat Prod. 2008. PMID: 18771244

4

BM6, a new semi-synthetic vinca alkaloid, exhibits its potent in vivo anti-tumor activities via its high binding affinity for tubulin and improved pharmacokinetic profiles.

Li W, Shao Y, Hu L, Zhang X, Chen Y, Tong L, Li C, Shen X, Ding J. Li W, et al. Among authors: hu l. Cancer Biol Ther. 2007 May;6(5):787-94. doi: 10.4161/cbt.6.5.4006. Epub 2007 Feb 14. Cancer Biol Ther. 2007. PMID: 17387272 Free article.

5

Cytotoxic withanolides from Physalis angulata L.

He QP, Ma L, Luo JY, He FY, Lou LG, Hu LH. He QP, et al. Among authors: hu lh. Chem Biodivers. 2007 Mar;4(3):443-9. doi: 10.1002/cbdv.200790036. Chem Biodivers. 2007. PMID: 17372946

6

Danthron functions as a retinoic X receptor antagonist by stabilizing tetramers of the receptor.

Zhang H, Zhou R, Li L, Chen J, Chen L, Li C, Ding H, Yu L, Hu L, Jiang H, Shen X. Zhang H, et al. Among authors: hu l. J Biol Chem. 2011 Jan 21;286(3):1868-75. doi: 10.1074/jbc.M110.166215. Epub 2010 Nov 17. J Biol Chem. 2011. PMID: 21084305 Free PMC article.

7

The effect of vindoline C-16 substituents on the biomimetic coupling reaction: synthesis and cytotoxicity evaluation of the corresponding vinorelbine analogues.

Song W, Hu L, Meng Y, Ma L, Guo D, Liu X, Hu L. Song W, et al. Among authors: hu l. Bioorg Med Chem Lett. 2012 May 15;22(10):3485-7. doi: 10.1016/j.bmcl.2012.03.082. Epub 2012 Mar 29. Bioorg Med Chem Lett. 2012. PMID: 22525316

8

Synthesis and structure-activity relationship studies of cytotoxic vinorelbine amide analogues.

Hu L, Song W, Meng Y, Guo D, Liu X, Hu L. Hu L, et al. Bioorg Med Chem Lett. 2012 Dec 15;22(24):7547-50. doi: 10.1016/j.bmcl.2012.10.024. Epub 2012 Oct 17. Bioorg Med Chem Lett. 2012. PMID: 23107481

9

Synthesis and cytotoxicity evaluation of 4-amino-4-dehydroxylarctigenin derivatives in glucose-starved A549 tumor cells.

Lei M, Gan X, Zhao K, Yu Q, Hu L. Lei M, et al. Among authors: hu l. Bioorg Med Chem Lett. 2015 Feb 1;25(3):435-7. doi: 10.1016/j.bmcl.2014.12.061. Epub 2014 Dec 24. Bioorg Med Chem Lett. 2015. PMID: 25571795

10

Synthesis and structure-activity relationships of boswellic acid derivatives as potent VEGFR-2 inhibitors.

Shen S, Xu X, Liu Z, Liu J, Hu L. Shen S, et al. Among authors: hu l. Bioorg Med Chem. 2015 May 1;23(9):1982-93. doi: 10.1016/j.bmc.2015.03.022. Epub 2015 Mar 14. Bioorg Med Chem. 2015. PMID: 25819335

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