Shi W - Search Results

1

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

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

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

4

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

5

Discovery of novel pyrrole-based scaffold as potent and orally bioavailable free fatty acid receptor 1 agonists for the treatment of type 2 diabetes.

Li Z, Pan M, Su X, Dai Y, Fu M, Cai X, Shi W, Huang W, Qian H. Li Z, et al. Among authors: shi w. Bioorg Med Chem. 2016 May 1;24(9):1981-7. doi: 10.1016/j.bmc.2016.03.014. Epub 2016 Mar 7. Bioorg Med Chem. 2016. PMID: 27020683

6

Natural products as sources of new fungicides (III): Antifungal activity of 2,4-dihydroxy-5-methylacetophenone derivatives.

Shi W, Dan WJ, Tang JJ, Zhang Y, Nandinsuren T, Zhang AL, Gao JM. Shi W, et al. Bioorg Med Chem Lett. 2016 May 1;26(9):2156-8. doi: 10.1016/j.bmcl.2016.03.073. Epub 2016 Mar 18. Bioorg Med Chem Lett. 2016. PMID: 27025344

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 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

9

Design, synthesis and cytotoxic activities of scopoletin-isoxazole and scopoletin-pyrazole hybrids.

Shi W, Hu J, Bao N, Li D, Chen L, Sun J. Shi W, et al. Bioorg Med Chem Lett. 2017 Jan 15;27(2):147-151. doi: 10.1016/j.bmcl.2016.11.089. Epub 2016 Dec 1. Bioorg Med Chem Lett. 2017. PMID: 27956344

10

A novel mitochondria-targeting fluorescent probe for hydrogen sulfide in living cells.

Shi W, Pan M, Qiang H, Qiu Q, Huang W, Lin H, Qian H, Ge L. Shi W, et al. Chem Biol Drug Des. 2017 Aug;90(2):167-174. doi: 10.1111/cbdd.12948. Epub 2017 Feb 28. Chem Biol Drug Des. 2017. PMID: 28109134

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