Wang Y - Search Results

1

Direct inhibition of microglial activation by a μ receptor selective agonist alleviates inflammatory-induced pain hypersensitivity.

Wang J, Ru QM, Yu XH, Wang C, Li K, Han CZ, Li N, Zhao J, Wood JN, Liu X, Wang R, Wang Y. Wang J, et al. Among authors: wang y, wang c, wang r. Eur J Pharmacol. 2023 Dec 15;961:176182. doi: 10.1016/j.ejphar.2023.176182. Epub 2023 Nov 10. Eur J Pharmacol. 2023. PMID: 37951488

2

Highly enantioselective conjugate additions of phosphites to alpha,beta-unsaturated N-acylpyrroles and imines: a practical approach to enantiomerically enriched amino phosphonates.

Zhao D, Wang Y, Mao L, Wang R. Zhao D, et al. Among authors: wang y, wang r. Chemistry. 2009 Oct 19;15(41):10983-7. doi: 10.1002/chem.200901901. Chemistry. 2009. PMID: 19739227

3

Catalytic asymmetric hydrophosphinylation of alpha,beta-unsaturated N-acylpyrroles: application of dialkyl phosphine oxides in enantioselective synthesis of chiral phosphine oxides or phosphines.

Zhao D, Mao L, Wang Y, Yang D, Zhang Q, Wang R. Zhao D, et al. Among authors: wang y, wang r. Org Lett. 2010 Apr 16;12(8):1880-2. doi: 10.1021/ol100504h. Org Lett. 2010. PMID: 20337436

4

A new class of highly potent and selective endomorphin-1 analogues containing α-methylene-β-aminopropanoic acids (map).

Wang Y, Xing Y, Liu X, Ji H, Kai M, Chen Z, Yu J, Zhao D, Ren H, Wang R. Wang Y, et al. Among authors: wang r. J Med Chem. 2012 Jul 12;55(13):6224-36. doi: 10.1021/jm300664y. Epub 2012 Jul 2. J Med Chem. 2012. PMID: 22724433

5

Design, synthesis, and pharmacological characterization of novel endomorphin-1 analogues as extremely potent μ-opioid agonists.

Liu X, Wang Y, Xing Y, Yu J, Ji H, Kai M, Wang Z, Wang D, Zhang Y, Zhao D, Wang R. Liu X, et al. Among authors: wang z, wang y, wang d, wang r. J Med Chem. 2013 Apr 11;56(7):3102-14. doi: 10.1021/jm400195y. Epub 2013 Mar 28. J Med Chem. 2013. PMID: 23477419

6

Characterization of opioid activities of endomorphin analogs with C-terminal amide to hydrazide conversion.

Wang CL, Ren YK, Xiang Q, Wang Y, Gu N, Lu C, Wang R. Wang CL, et al. Among authors: wang y, wang r. Neuropeptides. 2013 Oct;47(5):297-304. doi: 10.1016/j.npep.2013.09.001. Epub 2013 Sep 19. Neuropeptides. 2013. PMID: 24084335

7

Endomorphin-1 analogues (MELs) penetrate the blood-brain barrier and exhibit good analgesic effects with minimal side effects.

Wang Y, Liu X, Wang D, Yang J, Zhao L, Yu J, Wang R. Wang Y, et al. Among authors: wang d, wang r. Neuropharmacology. 2015 Oct;97:312-21. doi: 10.1016/j.neuropharm.2015.06.010. Epub 2015 Jun 24. Neuropharmacology. 2015. PMID: 26116761

8

Design, synthesis, and evaluation of new endomorphin analogs with enhanced central antinociception after peripheral administration.

Liu X, Zhao L, Wang Y, Mou L, Yang J, Zhang Y, Wang D, Wang R. Liu X, et al. Among authors: wang y, wang d, wang r. Bioorg Med Chem Lett. 2015 Nov 15;25(22):5393-7. doi: 10.1016/j.bmcl.2015.09.025. Epub 2015 Sep 11. Bioorg Med Chem Lett. 2015. PMID: 26403932

9

Endomorphin-1 attenuates Aβ42 induced impairment of novel object and object location recognition tasks in mice.

Zhang RS, Xu HJ, Jiang JH, Han RW, Chang M, Peng YL, Wang Y, Wang R. Zhang RS, et al. Among authors: wang y, wang r. Brain Res. 2015 Dec 10;1629:210-20. doi: 10.1016/j.brainres.2015.10.028. Epub 2015 Oct 23. Brain Res. 2015. PMID: 26505914

10

Structure-constrained endomorphin analogs display differential antinociceptive mechanisms in mice after spinal administration.

Wang Y, Zhou J, Liu X, Zhao L, Wang Z, Zhang X, Wang K, Wang L, Wang R. Wang Y, et al. Among authors: wang l, wang k, wang z, wang r. Peptides. 2017 May;91:40-48. doi: 10.1016/j.peptides.2017.03.009. Epub 2017 Mar 29. Peptides. 2017. PMID: 28363796

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