Lin B - Search Results

1

Synthesis and biological evaluation of NH₂-acyl oseltamivir analogues as potent neuraminidase inhibitors.

Wang K, Yang F, Wang L, Liu K, Sun L, Lin B, Hu Y, Wang B, Cheng M, Tian Y. Wang K, et al. Among authors: lin b. Eur J Med Chem. 2017 Dec 1;141:648-656. doi: 10.1016/j.ejmech.2017.10.004. Epub 2017 Oct 5. Eur J Med Chem. 2017. PMID: 29107426

2

Molecular recognition of CYP26A1 binding pockets and structure-activity relationship studies for design of potent and selective retinoic acid metabolism blocking agents.

Sun B, Song S, Hao CZ, Huang WX, Liu CC, Xie HL, Lin B, Cheng MS, Zhao DM. Sun B, et al. Among authors: lin b. J Mol Graph Model. 2015 Mar;56:10-9. doi: 10.1016/j.jmgm.2014.11.014. Epub 2014 Dec 8. J Mol Graph Model. 2015. PMID: 25541526

3

Design, synthesis and biological evaluation of 1-phenanthryl-tetrahydroisoquinoline derivatives as novel p21-activated kinase 4 (PAK4) inhibitors.

Song S, Li X, Guo J, Hao C, Feng Y, Guo B, Liu T, Zhang Q, Zhang Z, Li R, Wang J, Lin B, Li F, Zhao D, Cheng M. Song S, et al. Among authors: lin b. Org Biomol Chem. 2015 Mar 28;13(12):3803-18. doi: 10.1039/c5ob00037h. Org Biomol Chem. 2015. PMID: 25705811

4

Design, synthesis, and biological evaluation of amide imidazole derivatives as novel metabolic enzyme CYP26A1 inhibitors.

Sun B, Liu K, Han J, Zhao LY, Su X, Lin B, Zhao DM, Cheng MS. Sun B, et al. Among authors: lin b. Bioorg Med Chem. 2015 Oct 15;23(20):6763-73. doi: 10.1016/j.bmc.2015.08.019. Epub 2015 Aug 20. Bioorg Med Chem. 2015. PMID: 26365710

5

The semi-synthesis of novel andrographolide analogues and anti-influenza virus activity evaluation of their derivatives.

Yuan L, Zhang C, Sun H, Liu Q, Huang J, Sheng L, Lin B, Wang J, Chen L. Yuan L, et al. Among authors: lin b. Bioorg Med Chem Lett. 2016 Feb 1;26(3):769-773. doi: 10.1016/j.bmcl.2015.12.100. Epub 2015 Dec 29. Bioorg Med Chem Lett. 2016. PMID: 26791013

6

Discovery of novel N,N-3-phenyl-3-benzylaminopropionanilides as potent inhibitors of cholesteryl ester transfer protein in vivo.

Xie H, Li Y, Bai C, Wang R, Liu C, Hao C, Lin B, Cheng M, Zhao D. Xie H, et al. Among authors: lin b. Bioorg Med Chem. 2016 Apr 15;24(8):1811-8. doi: 10.1016/j.bmc.2016.03.002. Epub 2016 Mar 2. Bioorg Med Chem. 2016. PMID: 26993745

7

Design, synthesis and biological evaluation of N,N-3-phenyl-3-benzylaminopropanamide derivatives as novel cholesteryl ester transfer protein inhibitor.

Zhao D, Xie H, Bai C, Liu C, Hao C, Zhao S, Yuan H, Luo C, Wang J, Lin B, Zheng J, Cheng M. Zhao D, et al. Among authors: lin b. Bioorg Med Chem. 2016 Apr 15;24(8):1589-97. doi: 10.1016/j.bmc.2015.12.010. Epub 2015 Dec 8. Bioorg Med Chem. 2016. PMID: 27010500

8

Advances in the 1-phenanthryl-tetrahydroisoquinoline series of PAK4 inhibitors: potent agents restrain tumor cell growth and invasion.

Hao C, Li X, Song S, Guo B, Guo J, Zhang J, Zhang Q, Huang W, Wang J, Lin B, Cheng M, Li F, Zhao D. Hao C, et al. Among authors: lin b. Org Biomol Chem. 2016 Aug 10;14(32):7676-90. doi: 10.1039/c6ob01072e. Org Biomol Chem. 2016. PMID: 27454186

9

A Au(i)-catalyzed hydrogen bond-directed tandem strategy to synthesize indeno-chromen-4-one and indeno-quinolin-4-one derivatives.

Jiang C, Xiong Z, Jin S, Gao P, Tang Y, Wang Y, Du C, Wang X, Liu Y, Lin B, Liu Y, Cheng M. Jiang C, et al. Among authors: lin b. Chem Commun (Camb). 2016 Oct 4;52(77):11516-9. doi: 10.1039/c6cc05391b. Epub 2016 Aug 22. Chem Commun (Camb). 2016. PMID: 27545584

10

Dual-tail approach to discovery of novel carbonic anhydrase IX inhibitors by simultaneously matching the hydrophobic and hydrophilic halves of the active site.

Hou Z, Lin B, Bao Y, Yan HN, Zhang M, Chang XW, Zhang XX, Wang ZJ, Wei GF, Cheng MS, Liu Y, Guo C. Hou Z, et al. Among authors: lin b. Eur J Med Chem. 2017 May 26;132:1-10. doi: 10.1016/j.ejmech.2017.03.023. Epub 2017 Mar 16. Eur J Med Chem. 2017. PMID: 28334643

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