Huang ZS - Search Results

1

Design, synthesis and structure-activity relationship of novel 2-pyrimidinylindole derivatives as orally available anti-obesity agents.

Wei LY, Lin YW, Luo JC, Li YX, Hu YT, Guo SY, Jiang Z, Zhao DD, Chen SB, Huang ZS. Wei LY, et al. Among authors: huang zs. Eur J Med Chem. 2024 Nov 5;277:116773. doi: 10.1016/j.ejmech.2024.116773. Epub 2024 Aug 16. Eur J Med Chem. 2024. PMID: 39163779

2

Synthesis and cytotoxicity study of alkannin derivatives.

Huang ZS, Wu HQ, Duan ZF, Xie BF, Liu ZC, Feng GK, Gu LQ, Chan AS, Li YM. Huang ZS, et al. Eur J Med Chem. 2004 Sep;39(9):755-64. doi: 10.1016/j.ejmech.2004.05.004. Eur J Med Chem. 2004. PMID: 15337288

3

The molecular mechanisms involved in the cytotoxicity of alkannin derivatives.

Wu HQ, Huang ZS, Bu XZ, Shen YD, Zhang ZL, Xie BF, Liu ZC, Gu LQ, Chan AS. Wu HQ, et al. Among authors: huang zs. Eur J Med Chem. 2005 Dec;40(12):1341-5. doi: 10.1016/j.ejmech.2005.05.004. Epub 2005 Jun 29. Eur J Med Chem. 2005. PMID: 15992967

4

Synthesis and biological evaluation of functionalized coumarins as acetylcholinesterase inhibitors.

Shen Q, Peng Q, Shao J, Liu X, Huang Z, Pu X, Ma L, Li YM, Chan AS, Gu L. Shen Q, et al. Eur J Med Chem. 2005 Dec;40(12):1307-15. doi: 10.1016/j.ejmech.2005.07.014. Epub 2005 Sep 21. Eur J Med Chem. 2005. PMID: 16182411

5

Synthesis and evaluation of quindoline derivatives as G-quadruplex inducing and stabilizing ligands and potential inhibitors of telomerase.

Zhou JL, Lu YJ, Ou TM, Zhou JM, Huang ZS, Zhu XF, Du CJ, Bu XZ, Ma L, Gu LQ, Li YM, Chan AS. Zhou JL, et al. Among authors: huang zs. J Med Chem. 2005 Nov 17;48(23):7315-21. doi: 10.1021/jm050041b. J Med Chem. 2005. PMID: 16279791

6

Alpha-glucosidase inhibition of natural curcuminoids and curcumin analogs.

Du ZY, Liu RR, Shao WY, Mao XP, Ma L, Gu LQ, Huang ZS, Chan AS. Du ZY, et al. Among authors: huang zs. Eur J Med Chem. 2006 Feb;41(2):213-8. doi: 10.1016/j.ejmech.2005.10.012. Epub 2006 Jan 4. Eur J Med Chem. 2006. PMID: 16387392

7

Spectroscopic studies of DNA binding modes of cation-substituted anthrapyrazoles derived from emodin.

Tan JH, Lu YJ, Huang ZS, Gu LQ, Wu JY. Tan JH, et al. Among authors: huang zs. Eur J Med Chem. 2007 Sep;42(9):1169-75. doi: 10.1016/j.ejmech.2007.02.002. Epub 2007 Feb 25. Eur J Med Chem. 2007. PMID: 17408812

8

Oxoisoaporphine alkaloid derivatives: synthesis, DNA binding affinity and cytotoxicity.

Tang H, Wang XD, Wei YB, Huang SL, Huang ZS, Tan JH, An LK, Wu JY, Chan AS, Gu LQ. Tang H, et al. Among authors: huang sl, huang zs. Eur J Med Chem. 2008 May;43(5):973-80. doi: 10.1016/j.ejmech.2007.07.004. Epub 2007 Jul 15. Eur J Med Chem. 2008. PMID: 17720282

9

Synthesis, cytotoxic activities and structure-activity relationships of topoisomerase I inhibitors: indolizinoquinoline-5,12-dione derivatives.

Cheng Y, An LK, Wu N, Wang XD, Bu XZ, Huang ZS, Gu LQ. Cheng Y, et al. Among authors: huang zs. Bioorg Med Chem. 2008 Apr 15;16(8):4617-25. doi: 10.1016/j.bmc.2008.02.036. Epub 2008 Feb 15. Bioorg Med Chem. 2008. PMID: 18296054

10

Design, synthesis and evaluation of isaindigotone derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors.

Pan L, Tan JH, Hou JQ, Huang SL, Gu LQ, Huang ZS. Pan L, et al. Among authors: huang sl, huang zs. Bioorg Med Chem Lett. 2008 Jul 1;18(13):3790-3. doi: 10.1016/j.bmcl.2008.05.039. Epub 2008 May 16. Bioorg Med Chem Lett. 2008. PMID: 18524585

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