Huang SL - Search Results

1

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

2

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: huang sl, huang zs. 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

3

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

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: huang sl, huang zs. 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: huang sl, huang zs. 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, biological evaluation and molecular modeling of oxoisoaporphine and oxoaporphine derivatives as new dual inhibitors of acetylcholinesterase/butyrylcholinesterase.

Tang H, Wei YB, Zhang C, Ning FX, Qiao W, Huang SL, Ma L, Huang ZS, Gu LQ. Tang H, et al. Among authors: huang sl, huang zs. Eur J Med Chem. 2009 Jun;44(6):2523-32. doi: 10.1016/j.ejmech.2009.01.021. Epub 2009 Jan 31. Eur J Med Chem. 2009. PMID: 19243862

7

Isaindigotone derivatives: a new class of highly selective ligands for telomeric G-quadruplex DNA.

Tan JH, Ou TM, Hou JQ, Lu YJ, Huang SL, Luo HB, Wu JY, Huang ZS, Wong KY, Gu LQ. Tan JH, et al. Among authors: huang sl, huang zs. J Med Chem. 2009 May 14;52(9):2825-35. doi: 10.1021/jm801600m. J Med Chem. 2009. PMID: 19354252

8

Synthesis and evaluation of 9-O-substituted berberine derivatives containing aza-aromatic terminal group as highly selective telomeric G-quadruplex stabilizing ligands.

Ma Y, Ou TM, Tan JH, Hou JQ, Huang SL, Gu LQ, Huang ZS. Ma Y, et al. Among authors: huang sl, huang zs. Bioorg Med Chem Lett. 2009 Jul 1;19(13):3414-7. doi: 10.1016/j.bmcl.2009.05.030. Epub 2009 May 14. Bioorg Med Chem Lett. 2009. PMID: 19477640

9

Synthesis and antimultidrug resistance evaluation of icariin and its derivatives.

Liu DF, Li YP, Ou TM, Huang SL, Gu LQ, Huang M, Huang ZS. Liu DF, et al. Among authors: huang m, huang sl, huang zs. Bioorg Med Chem Lett. 2009 Aug 1;19(15):4237-40. doi: 10.1016/j.bmcl.2009.05.103. Epub 2009 May 30. Bioorg Med Chem Lett. 2009. PMID: 19523827

10

Synthesis and evaluation of novel rutaecarpine derivatives and related alkaloids derivatives as selective acetylcholinesterase inhibitors.

Wang B, Mai YC, Li Y, Hou JQ, Huang SL, Ou TM, Tan JH, An LK, Li D, Gu LQ, Huang ZS. Wang B, et al. Among authors: huang sl, huang zs. Eur J Med Chem. 2010 Apr;45(4):1415-23. doi: 10.1016/j.ejmech.2009.12.044. Epub 2010 Jan 4. Eur J Med Chem. 2010. PMID: 20079560

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