Bi Y - Search Results

1

Synthesis and biological activity of 28-amide derivatives of 23-hydroxy betulinic Acid as antitumor agent candidates.

Bi Y, Xu J, Sun F, Wu X, Ye W, Sun Y, Huang W. Bi Y, et al. Med Chem. 2013 Nov;9(7):920-5. doi: 10.2174/1573406411309070005. Med Chem. 2013. PMID: 23083117

2

Synthesis and cytotoxic activity of 17-carboxylic acid modified 23-hydroxy betulinic acid ester derivatives.

Bi Y, Xu J, Wu X, Ye W, Yuan S, Zhang L. Bi Y, et al. Bioorg Med Chem Lett. 2007 Mar 1;17(5):1475-8. doi: 10.1016/j.bmcl.2006.09.096. Epub 2006 Oct 4. Bioorg Med Chem Lett. 2007. PMID: 17275295

3

Synthesis and biological activity of 2-alkylbenzimidazoles bearing a N-phenylpyrrole moiety as novel angiotensin II AT1 receptor antagonists.

Xu JY, Zeng Y, Ran Q, Wei Z, Bi Y, He QH, Wang QJ, Hu S, Zhang J, Tang MY, Hua WY, Wu XM. Xu JY, et al. Among authors: bi y. Bioorg Med Chem Lett. 2007 May 15;17(10):2921-6. doi: 10.1016/j.bmcl.2007.02.042. Epub 2007 Feb 20. Bioorg Med Chem Lett. 2007. PMID: 17412584

4

Terpenoids. III: Synthesis and biological evaluation of 23-hydroxybetulinic acid derivatives as novel inhibitors of glycogen phosphorylase.

Zhu P, Bi Y, Xu J, Li Z, Liu J, Zhang L, Ye W, Wu X. Zhu P, et al. Among authors: bi y. Bioorg Med Chem Lett. 2009 Dec 15;19(24):6966-9. doi: 10.1016/j.bmcl.2009.10.055. Epub 2009 Nov 2. Bioorg Med Chem Lett. 2009. PMID: 19889536

5

Synthesis and biological activity of 23-hydroxybetulinic acid C-28 ester derivatives as antitumor agent candidates.

Bi Y, Xu J, Sun F, Wu X, Ye W, Sun Y, Huang W. Bi Y, et al. Molecules. 2012 Jul 25;17(8):8832-41. doi: 10.3390/molecules17088832. Molecules. 2012. PMID: 22832884 Free PMC article.

6

Synthesis, antifungal activity, and molecular docking studies of novel triazole derivatives.

Wang N, Chai X, Chen Y, Zhang L, Li W, Gao Y, Bi Y, Yu S, Meng Q. Wang N, et al. Among authors: bi y. Med Chem. 2013 May;9(3):384-8. doi: 10.2174/1573406411309030009. Med Chem. 2013. PMID: 22921110

7

Synthesis and biological evaluation of novel ocotillol-type triterpenoid derivatives as antibacterial agents.

Zhou Z, Ma C, Zhang H, Bi Y, Chen X, Tian H, Xie X, Meng Q, Lewis PJ, Xu J. Zhou Z, et al. Among authors: bi y. Eur J Med Chem. 2013 Oct;68:444-53. doi: 10.1016/j.ejmech.2013.07.041. Epub 2013 Aug 9. Eur J Med Chem. 2013. PMID: 23994872

8

Novel 3-substituted ocotillol-type triterpenoid derivatives as antibacterial candidates.

Bi Y, Ma C, Zhang H, Zhou Z, Yang J, Zhang Z, Meng Q, Lewis PJ, Xu J. Bi Y, et al. Chem Biol Drug Des. 2014 Oct;84(4):489-96. doi: 10.1111/cbdd.12337. Epub 2014 May 20. Chem Biol Drug Des. 2014. PMID: 24811479

9

Design, synthesis, nitric oxide release and antibacterial evaluation of novel nitrated ocotillol-type derivatives.

Bi Y, Yang X, Zhang T, Liu Z, Zhang X, Lu J, Cheng K, Xu J, Wang H, Lv G, Lewis PJ, Meng Q, Ma C. Bi Y, et al. Eur J Med Chem. 2015 Aug 28;101:71-80. doi: 10.1016/j.ejmech.2015.06.021. Epub 2015 Jun 17. Eur J Med Chem. 2015. PMID: 26114813

10

Design and synthesis of 28-hydroxy protopanaxadiol as a novel probe template.

Liu ZY, Zhang HY, Bi Y, Liu XX, Lu J, Zhang XC, Xu JY, Wang CZ, Yuan CS. Liu ZY, et al. Among authors: bi y. Nat Prod Res. 2017 Jul;31(13):1523-1528. doi: 10.1080/14786419.2017.1280488. Epub 2017 Jan 20. Nat Prod Res. 2017. PMID: 28107791

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