Wang R - Search Results

1

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

2

Study in vitro and in vivo of nociceptin/orphanin FQ(1-13)NH2 analogues substituting N-Me-Gly for Gly2 or Gly3.

Chen LX, Fang Q, Chen Q, Guo J, Wang ZZ, Chen Y, Wang R. Chen LX, et al. Among authors: wang zz, wang r. Peptides. 2004 Aug;25(8):1349-54. doi: 10.1016/j.peptides.2004.05.012. Peptides. 2004. PMID: 15350703

3

Cardiovascular effects of endomorphins in alloxan-induced diabetic rats.

Liu J, Yu Y, Fan YZ, Chang H, Liu HM, Cui Y, Chen Q, Wang R. Liu J, et al. Among authors: wang r. Peptides. 2005 Apr;26(4):607-14. doi: 10.1016/j.peptides.2004.11.017. Epub 2004 Dec 30. Peptides. 2005. PMID: 15752575

4

Structure-activity relationship of the novel bivalent and C-terminal modified analogues of endomorphin-2.

Gao Y, Liu X, Wei J, Zhu B, Chen Q, Wang R. Gao Y, et al. Among authors: wang r. Bioorg Med Chem Lett. 2005 Apr 1;15(7):1847-50. doi: 10.1016/j.bmcl.2005.02.021. Bioorg Med Chem Lett. 2005. PMID: 15780619

5

Neuropeptide FF receptors exert contractile activity via inhibition of nitric oxide release in the mouse distal colon.

Fang Q, Guo J, Chang M, Chen LX, Chen Q, Wang R. Fang Q, et al. Among authors: wang r. Peptides. 2005 May;26(5):791-7. doi: 10.1016/j.peptides.2004.12.009. Epub 2005 Jan 18. Peptides. 2005. PMID: 15808909

6

Melatonin enhances antinociceptive effects of delta-, but not mu-opioid agonist in mice.

Li SR, Wang T, Wang R, Dai X, Chen Q, Li RD. Li SR, et al. Among authors: wang t, wang r. Brain Res. 2005 May 10;1043(1-2):132-8. doi: 10.1016/j.brainres.2005.02.067. Brain Res. 2005. PMID: 15862526

7

Endomorphin 1[psi] and endomorphin 2[psi], endomorphins analogues containing a reduced (CH2NH) amide bond between Tyr1 and Pro2, display partial agonist potency but significant antinociception.

Zhao QY, Chen Q, Yang DJ, Feng Y, Long Y, Wang P, Wang R. Zhao QY, et al. Among authors: wang p, wang r. Life Sci. 2005 Jul 22;77(10):1155-65. doi: 10.1016/j.lfs.2005.03.005. Life Sci. 2005. PMID: 15878600

8

Structure-activity studies on different modifications of nociceptin/orphanin FQ: identification of highly potent agonists and antagonists of its receptor.

Chang M, Peng YL, Dong SL, Han RW, Li W, Yang DJ, Chen Q, Wang R. Chang M, et al. Among authors: wang r. Regul Pept. 2005 Sep 15;130(3):116-22. doi: 10.1016/j.regpep.2005.04.005. Regul Pept. 2005. PMID: 15935490

9

Structure-activity relationships of novel endomorphin-2 analogues with N-O turns induced by alpha-aminoxy acids.

Wei J, Shao X, Gong M, Zhu B, Cui Y, Gao Y, Wang R. Wei J, et al. Among authors: wang r. Bioorg Med Chem Lett. 2005 Jun 15;15(12):2986-9. doi: 10.1016/j.bmcl.2005.04.050. Bioorg Med Chem Lett. 2005. PMID: 15984054

10

C-terminal amide to alcohol conversion changes the cardiovascular effects of endomorphins in anesthetized rats.

Yu Y, Wang CL, Cui Y, Fan YZ, Liu J, Shao X, Liu HM, Wang R. Yu Y, et al. Among authors: wang r, wang cl. Peptides. 2006 Jan;27(1):136-43. doi: 10.1016/j.peptides.2005.07.006. Epub 2005 Sep 1. Peptides. 2006. PMID: 16139930

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