Hu Y - Search Results

1

Non-steroidal pregnancy-terminating agents: design, synthesis and structure-activity relationships of 2-aryl-1,2,4-triazolo[1,5-a]pyridine.

Liu T, Hu Y. Liu T, et al. Among authors: hu y. Bioorg Med Chem Lett. 2002 Sep 2;12(17):2411-3. doi: 10.1016/s0960-894x(02)00399-2. Bioorg Med Chem Lett. 2002. PMID: 12161145

2

Nitrogen-containing flavonoids as CDK1/Cyclin B inhibitors: design, synthesis, and biological evaluation.

Liu T, Xu Z, He Q, Chen Y, Yang B, Hu Y. Liu T, et al. Among authors: hu y. Bioorg Med Chem Lett. 2007 Jan 1;17(1):278-81. doi: 10.1016/j.bmcl.2006.07.088. Epub 2006 Nov 7. Bioorg Med Chem Lett. 2007. PMID: 17085048

3

Identification of SVM-based classification model, synthesis and evaluation of prenylated flavonoids as vasorelaxant agents.

Dong X, Liu Y, Yan J, Jiang C, Chen J, Liu T, Hu Y. Dong X, et al. Among authors: hu y. Bioorg Med Chem. 2008 Sep 1;16(17):8151-60. doi: 10.1016/j.bmc.2008.07.031. Epub 2008 Jul 20. Bioorg Med Chem. 2008. PMID: 18678502

4

Synthesis, biological evaluation and quantitative structure-activities relationship of flavonoids as vasorelaxant agents.

Dong X, Liu T, Yan J, Wu P, Chen J, Hu Y. Dong X, et al. Among authors: hu y. Bioorg Med Chem. 2009 Jan 15;17(2):716-26. doi: 10.1016/j.bmc.2008.11.052. Epub 2008 Nov 24. Bioorg Med Chem. 2009. PMID: 19070497

5

Design, synthesis, and quantitative structure-activity relationship of cytotoxic gamma-carboline derivatives.

Chen J, Dong X, Liu T, Lou J, Jiang C, Huang W, He Q, Yang B, Hu Y. Chen J, et al. Among authors: hu y. Bioorg Med Chem. 2009 May 1;17(9):3324-31. doi: 10.1016/j.bmc.2009.03.037. Epub 2009 Mar 26. Bioorg Med Chem. 2009. PMID: 19359185

6

Synthesis and biological evaluation of 3,4-diaryl-5-aminoisoxazole derivatives.

Liu T, Dong X, Xue N, Wu R, He Q, Yang B, Hu Y. Liu T, et al. Among authors: hu y. Bioorg Med Chem. 2009 Sep 1;17(17):6279-85. doi: 10.1016/j.bmc.2009.07.040. Epub 2009 Jul 23. Bioorg Med Chem. 2009. PMID: 19665898

7

Synthesis and biological evaluation of novel hybrid chalcone derivatives as vasorelaxant agents.

Dong X, Du L, Pan Z, Liu T, Yang B, Hu Y. Dong X, et al. Among authors: hu y. Eur J Med Chem. 2010 Sep;45(9):3986-92. doi: 10.1016/j.ejmech.2010.05.054. Epub 2010 Jun 2. Eur J Med Chem. 2010. PMID: 20566231

8

Pharmacophore identification, synthesis, and biological evaluation of carboxylated chalcone derivatives as CysLT1 antagonists.

Dong X, Wang L, Huang X, Liu T, Wei E, Du L, Yang B, Hu Y. Dong X, et al. Among authors: hu y. Bioorg Med Chem. 2010 Aug 1;18(15):5519-27. doi: 10.1016/j.bmc.2010.06.047. Epub 2010 Jun 20. Bioorg Med Chem. 2010. PMID: 20621485

9

Design, synthesis, and biological evaluation of novel N-γ-carboline arylsulfonamides as anticancer agents.

Chen J, Liu T, Wu R, Lou J, Cao J, Dong X, Yang B, He Q, Hu Y. Chen J, et al. Among authors: hu y. Bioorg Med Chem. 2010 Dec 15;18(24):8478-84. doi: 10.1016/j.bmc.2010.10.047. Epub 2010 Oct 25. Bioorg Med Chem. 2010. PMID: 21067933

10

Synthesis and biological evaluation of new 4β-anilino-4'-O-demethyl-4-desoxypodophyllotoxin derivatives as potential antitumor agents.

Wang L, Yang F, Yang X, Guan X, Hu C, Liu T, He Q, Yang B, Hu Y. Wang L, et al. Among authors: hu c, hu y. Eur J Med Chem. 2011 Jan;46(1):285-96. doi: 10.1016/j.ejmech.2010.11.016. Epub 2010 Nov 19. Eur J Med Chem. 2011. PMID: 21145139

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