Wan Y - Search Results

1

A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds.

Liu J, Cao R, Yi W, Ma C, Wan Y, Zhou B, Ma L, Song H. Liu J, et al. Among authors: wan y. Eur J Med Chem. 2009 Apr;44(4):1773-8. doi: 10.1016/j.ejmech.2008.04.002. Epub 2008 Apr 27. Eur J Med Chem. 2009. PMID: 18524420

2

Optical behaviors of conjugated-chain compounds containing benzene and furan units.

Pan WL, Song JG, Chen Y, Wan YQ, Song HC. Pan WL, et al. Among authors: wan yq. Spectrochim Acta A Mol Biomol Spectrosc. 2007 Apr;66(4-5):1300-6. doi: 10.1016/j.saa.2006.05.035. Epub 2006 Jun 27. Spectrochim Acta A Mol Biomol Spectrosc. 2007. PMID: 16920004

3

Synthesis and biological evaluation of helicid analogues as novel acetylcholinesterase inhibitors.

Wen H, Lin C, Que L, Ge H, Ma L, Cao R, Wan Y, Peng W, Wang Z, Song H. Wen H, et al. Among authors: wan y. Eur J Med Chem. 2008 Jan;43(1):166-73. doi: 10.1016/j.ejmech.2007.03.018. Epub 2007 Apr 5. Eur J Med Chem. 2008. PMID: 17574306

4

1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors.

Liu J, Yi W, Wan Y, Ma L, Song H. Liu J, et al. Among authors: wan y. Bioorg Med Chem. 2008 Feb 1;16(3):1096-102. doi: 10.1016/j.bmc.2007.10.102. Bioorg Med Chem. 2008. PMID: 18326070

5

Synthesis and biological evaluation of helicid analogues as mushroom tyrosinase inhibitors.

Yi W, Cao R, Wen H, Yan Q, Zhou B, Wan Y, Ma L, Song H. Yi W, et al. Among authors: wan y. Bioorg Med Chem Lett. 2008 Dec 15;18(24):6490-3. doi: 10.1016/j.bmcl.2008.10.056. Epub 2008 Oct 17. Bioorg Med Chem Lett. 2008. PMID: 18996693

6

Synthesis and optical behaviors of 2-(9-phenanthrenyl)-, 2-(9-anthryl)-, and 2-(1-pyrenyl)-1-alkylimidazole homologues.

Yan YN, Lin DY, Pan WL, Li XL, Wan YQ, Mai YL, Song HC. Yan YN, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2009 Sep 15;74(1):233-42. doi: 10.1016/j.saa.2009.06.020. Epub 2009 Jun 16. Spectrochim Acta A Mol Biomol Spectrosc. 2009. PMID: 19577952

7

Pyrrolo[2,3-c]azepine derivatives: a new class of potent protein tyrosine phosphatase 1B inhibitors.

Xie J, Tian J, Su L, Huang M, Zhu X, Ye F, Wan Y. Xie J, et al. Among authors: wan y. Bioorg Med Chem Lett. 2011 Jul 15;21(14):4306-9. doi: 10.1016/j.bmcl.2011.05.052. Epub 2011 May 27. Bioorg Med Chem Lett. 2011. PMID: 21696953

8

Toward potent α-glucosidase inhibitors based on xanthones: a closer look into the structure-activity correlations.

Li GL, He JY, Zhang A, Wan Y, Wang B, Chen WH. Li GL, et al. Among authors: wan y. Eur J Med Chem. 2011 Sep;46(9):4050-5. doi: 10.1016/j.ejmech.2011.06.003. Epub 2011 Jun 12. Eur J Med Chem. 2011. PMID: 21708415

9

Structure-based discovery of highly selective phosphodiesterase-9A inhibitors and implications for inhibitor design.

Meng F, Hou J, Shao YX, Wu PY, Huang M, Zhu X, Cai Y, Li Z, Xu J, Liu P, Luo HB, Wan Y, Ke H. Meng F, et al. Among authors: wan y. J Med Chem. 2012 Oct 11;55(19):8549-58. doi: 10.1021/jm301189c. Epub 2012 Oct 1. J Med Chem. 2012. PMID: 22985069 Free PMC article.

10

Design, synthesis and evaluation of N13-substituted evodiamine derivatives against human cancer cell lines.

Song S, Chen Z, Li S, Huang Y, Wan Y, Song H. Song S, et al. Among authors: wan y. Molecules. 2013 Dec 17;18(12):15750-68. doi: 10.3390/molecules181215750. Molecules. 2013. PMID: 24352027 Free PMC article.

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