Shi W - Search Results

1

Design, synthesis and antibacterial activity of 3-methylenepyrrolidine formyl hydroxyamino derivatives as novel peptide deformylase inhibitors.

Shi W, Ma H, Duan Y, Aubart K, Fang Y, Zonis R, Yang L, Hu W. Shi W, et al. Bioorg Med Chem Lett. 2011 Feb 1;21(3):1060-3. doi: 10.1016/j.bmcl.2010.11.102. Epub 2010 Nov 30. Bioorg Med Chem Lett. 2011. PMID: 21185180

2

Design, synthesis, and antibacterial activity of 2,5-dihydropyrrole formyl hydroxyamino derivatives as novel peptide deformylase inhibitors.

Shi W, Duan Y, Qian Y, Li M, Yang L, Hu W. Shi W, et al. Bioorg Med Chem Lett. 2010 Jun 15;20(12):3592-5. doi: 10.1016/j.bmcl.2010.04.123. Epub 2010 May 24. Bioorg Med Chem Lett. 2010. PMID: 20510610

3

Synthesis, antibacterial activity, and biological evaluation of formyl hydroxyamino derivatives as novel potent peptide deformylase inhibitors against drug-resistant bacteria.

Yang S, Shi W, Xing D, Zhao Z, Lv F, Yang L, Yang Y, Hu W. Yang S, et al. Among authors: shi w. Eur J Med Chem. 2014 Oct 30;86:133-52. doi: 10.1016/j.ejmech.2014.07.106. Epub 2014 Aug 12. Eur J Med Chem. 2014. PMID: 25151577

4

Design, synthesis and biological evaluation of novel 4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridine derivatives as potential BRD4 inhibitors.

Bi X, Li J, Li J, Shi W, Dai Y, Li Q, Zhang W, Huang W, Qian H, Jiang C. Bi X, et al. Among authors: shi w. Bioorg Med Chem. 2019 Jul 1;27(13):2813-2821. doi: 10.1016/j.bmc.2019.05.006. Epub 2019 May 7. Bioorg Med Chem. 2019. PMID: 31079968

5

Design, synthesis and biological evaluation of novel tetrahydroisoquinoline derivatives as P-glycoprotein-mediated multidrug resistance inhibitors.

Gao Y, Shi W, Cui J, Liu C, Bi X, Li Z, Huang W, Wang G, Qian H. Gao Y, et al. Among authors: shi w. Bioorg Med Chem. 2018 May 15;26(9):2420-2427. doi: 10.1016/j.bmc.2018.03.045. Epub 2018 Apr 3. Bioorg Med Chem. 2018. PMID: 29631786

6

Design, synthesis and biological evaluation of LBM-A5 derivatives as potent P-glycoprotein-mediated multidrug resistance inhibitors.

Wu Y, Pan M, Dai Y, Liu B, Cui J, Shi W, Qiu Q, Huang W, Qian H. Wu Y, et al. Among authors: shi w. Bioorg Med Chem. 2016 May 15;24(10):2287-97. doi: 10.1016/j.bmc.2016.03.065. Epub 2016 Apr 1. Bioorg Med Chem. 2016. PMID: 27073052

7

Design, synthesis and biological evaluation of 4-aminopyrimidine-5-cabaldehyde oximes as dual inhibitors of c-Met and VEGFR-2.

Qiang H, Gu W, Huang D, Shi W, Qiu Q, Dai Y, Huang W, Qian H. Qiang H, et al. Among authors: shi w. Bioorg Med Chem. 2016 Aug 15;24(16):3353-8. doi: 10.1016/j.bmc.2016.03.061. Epub 2016 Apr 1. Bioorg Med Chem. 2016. PMID: 27068889

8

Design, synthesis, and biological activity evaluation of a series of novel sulfonamide derivatives as BRD4 inhibitors against acute myeloid leukemia.

Feng Z, Chen A, Shi J, Zhou D, Shi W, Qiu Q, Liu X, Huang W, Li J, Qian H, Zhang W. Feng Z, et al. Among authors: shi j, shi w. Bioorg Chem. 2021 Jun;111:104849. doi: 10.1016/j.bioorg.2021.104849. Epub 2021 Mar 22. Bioorg Chem. 2021. PMID: 33798846

9

Design, synthesis and biological evaluation of N-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)-4-oxo-3,4-dihydrophthalazine-1-carboxamide derivatives as novel P-glycoprotein inhibitors reversing multidrug resistance.

Qiu Q, Zhou J, Shi W, Kairuki M, Huang W, Qian H. Qiu Q, et al. Among authors: shi w. Bioorg Chem. 2019 May;86:166-175. doi: 10.1016/j.bioorg.2019.01.039. Epub 2019 Jan 22. Bioorg Chem. 2019. PMID: 30710850

10

Design and synthesis of boron-containing diphenylpyrimidines as potent BTK and JAK3 dual inhibitors.

Ren J, Shi W, Zhao D, Wang Q, Chang X, He X, Wang X, Gao Y, Lu P, Zhang X, Xu H, Zhang Y. Ren J, et al. Among authors: shi w. Bioorg Med Chem. 2020 Jan 15;28(2):115236. doi: 10.1016/j.bmc.2019.115236. Epub 2019 Nov 30. Bioorg Med Chem. 2020. PMID: 31843459

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