Gu LQ - Search Results

1

Inhibition of thioredoxin reductase by curcumin analogs.

Liu Z, Du ZY, Huang ZS, Lee KS, Gu LQ. Liu Z, et al. Among authors: gu lq. Biosci Biotechnol Biochem. 2008 Aug;72(8):2214-8. doi: 10.1271/bbb.80229. Epub 2008 Aug 7. Biosci Biotechnol Biochem. 2008. PMID: 18685195 Free article.

2

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: gu lq. 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

3

Curcumin analogs as potent aldose reductase inhibitors.

Du ZY, Bao YD, Liu Z, Qiao W, Ma L, Huang ZS, Gu LQ, Chan AS. Du ZY, et al. Among authors: gu lq. Arch Pharm (Weinheim). 2006 Mar;339(3):123-8. doi: 10.1002/ardp.200500205. Arch Pharm (Weinheim). 2006. PMID: 16528793

4

Synthesis and evaluation of curcumin analogues as potential thioredoxin reductase inhibitors.

Qiu X, Liu Z, Shao WY, Liu X, Jing DP, Yu YJ, An LK, Huang SL, Bu XZ, Huang ZS, Gu LQ. Qiu X, et al. Among authors: gu lq. Bioorg Med Chem. 2008 Sep 1;16(17):8035-41. doi: 10.1016/j.bmc.2008.07.054. Epub 2008 Jul 24. Bioorg Med Chem. 2008. PMID: 18678491

5

Inhibition of thioredoxin reductase by mansonone F analogues: Implications for anticancer activity.

Liu Z, Huang SL, Li MM, Huang ZS, Lee KS, Gu LQ. Liu Z, et al. Among authors: gu lq. Chem Biol Interact. 2009 Jan 15;177(1):48-57. doi: 10.1016/j.cbi.2008.09.002. Epub 2008 Sep 7. Chem Biol Interact. 2009. PMID: 18822278

6

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: gu lq. J Med Chem. 2005 Nov 17;48(23):7315-21. doi: 10.1021/jm050041b. J Med Chem. 2005. PMID: 16279791

7

Derivatives of oxoisoaporphine alkaloids: a novel class of selective acetylcholinesterase inhibitors.

Tang H, Ning FX, Wei YB, Huang SL, Huang ZS, Chan AS, Gu LQ. Tang H, et al. Among authors: gu lq. Bioorg Med Chem Lett. 2007 Jul 1;17(13):3765-8. doi: 10.1016/j.bmcl.2007.04.015. Epub 2007 Apr 10. Bioorg Med Chem Lett. 2007. PMID: 17451950

8

9-Substituted berberine derivatives as G-quadruplex stabilizing ligands in telomeric DNA.

Zhang WJ, Ou TM, Lu YJ, Huang YY, Wu WB, Huang ZS, Zhou JL, Wong KY, Gu LQ. Zhang WJ, et al. Among authors: gu lq. Bioorg Med Chem. 2007 Aug 15;15(16):5493-501. doi: 10.1016/j.bmc.2007.05.050. Epub 2007 May 25. Bioorg Med Chem. 2007. PMID: 17574421

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: gu lq. 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: gu lq. 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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