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Journal Abstract Search

486 related items for PubMed ID: 8164255

  • 21. Reduced peptide bond cyclic somatostatin based opioid octapeptides. Synthesis, conformational properties and pharmacological characterization.
    Kazmierski WM, Ferguson RD, Knapp RJ, Lui GK, Yamamura HI, Hruby VJ.
    Int J Pept Protein Res; 1992 May; 39(5):401-14. PubMed ID: 1358847
    [Abstract] [Full Text] [Related]

  • 22. Beta-methyl substitution of cyclohexylalanine in Dmt-Tic-Cha-Phe peptides results in highly potent delta opioid antagonists.
    Tóth G, Ioja E, Tömböly C, Ballet S, Tourwé D, Péter A, Martinek T, Chung NN, Schiller PW, Benyhe S, Borsodi A.
    J Med Chem; 2007 Jan 25; 50(2):328-33. PubMed ID: 17228874
    [Abstract] [Full Text] [Related]

  • 23. Synthesis and characterization of potent and selective mu-opioid receptor antagonists, [Dmt(1), D-2-Nal(4)]endomorphin-1 (Antanal-1) and [Dmt(1), D-2-Nal(4)]endomorphin-2 (Antanal-2).
    Fichna J, do-Rego JC, Chung NN, Lemieux C, Schiller PW, Poels J, Broeck JV, Costentin J, Janecka A.
    J Med Chem; 2007 Feb 08; 50(3):512-20. PubMed ID: 17266203
    [Abstract] [Full Text] [Related]

  • 24. A novel cyclic opioid peptide analog showing high preference for mu-receptors.
    Schiller PW, Nguyen TM, Maziak L, Lemieux C.
    Biochem Biophys Res Commun; 1985 Mar 15; 127(2):558-64. PubMed ID: 2983726
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  • 25. The cis-4-amino-L-proline residue as a scaffold for the synthesis of cyclic and linear endomorphin-2 analogues.
    Mollica A, Pinnen F, Stefanucci A, Feliciani F, Campestre C, Mannina L, Sobolev AP, Lucente G, Davis P, Lai J, Ma SW, Porreca F, Hruby VJ.
    J Med Chem; 2012 Apr 12; 55(7):3027-35. PubMed ID: 22394120
    [Abstract] [Full Text] [Related]

  • 26. Pseudopeptide analogues of substance P and leucine enkephalinamide containing the psi (CH2O) modification: synthesis and biological activity.
    Roubini E, Laufer R, Gilon C, Selinger Z, Roques BP, Chorev M.
    J Med Chem; 1991 Aug 12; 34(8):2430-8. PubMed ID: 1714957
    [Abstract] [Full Text] [Related]

  • 27. Cyclic morphiceptin analogs: cyclization studies and opioid activities in vitro.
    Vogel D, Schmidt R, Hartung K, Demuth HU, Chung NN, Schiller PW.
    Int J Pept Protein Res; 1996 Dec 12; 48(6):495-502. PubMed ID: 8985782
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  • 28. Synthesis of stable and potent delta/mu opioid peptides: analogues of H-Tyr-c[D-Cys-Gly-Phe-D-Cys]-OH by ring-closing metathesis.
    Mollica A, Guardiani G, Davis P, Ma SW, Porreca F, Lai J, Mannina L, Sobolev AP, Hruby VJ.
    J Med Chem; 2007 Jun 28; 50(13):3138-42. PubMed ID: 17539621
    [Abstract] [Full Text] [Related]

  • 29. Antinociceptive potencies of beta-casomorphin analogs as compared to their affinities towards mu and delta opiate receptor sites in brain and periphery.
    Brantl V, Pfeiffer A, Herz A, Henschen A, Lottspeich F.
    Peptides; 1982 Jun 28; 3(5):793-7. PubMed ID: 6294635
    [Abstract] [Full Text] [Related]

  • 30. Synthesis, opioid receptor binding, and biological activities of naltrexone-derived pyrido- and pyrimidomorphinans.
    Ananthan S, Kezar HS, Carter RL, Saini SK, Rice KC, Wells JL, Davis P, Xu H, Dersch CM, Bilsky EJ, Porreca F, Rothman RB.
    J Med Chem; 1999 Sep 09; 42(18):3527-38. PubMed ID: 10479286
    [Abstract] [Full Text] [Related]

  • 31. Synthesis of highly mu and delta opioid receptor selective peptides containing a photoaffinity group.
    Landis G, Lui G, Shook JE, Yamamura HI, Burks TF, Hruby VJ.
    J Med Chem; 1989 Mar 09; 32(3):638-43. PubMed ID: 2537426
    [Abstract] [Full Text] [Related]

  • 32. Development of potent bifunctional endomorphin-2 analogues with mixed mu-/delta-opioid agonist and delta-opioid antagonist properties.
    Fujita Y, Tsuda Y, Li T, Motoyama T, Takahashi M, Shimizu Y, Yokoi T, Sasaki Y, Ambo A, Kita A, Jinsmaa Y, Bryant SD, Lazarus LH, Okada Y.
    J Med Chem; 2004 Jul 01; 47(14):3591-9. PubMed ID: 15214786
    [Abstract] [Full Text] [Related]

  • 33. Morphiceptin and beta-casomorphin-5 analogues containing a reduced peptide bond: selective mu-receptor agonists and a novel mu antagonist, H-Tyr-Pro psi (CH2-NH)Phe-Pro-Gly-OH.
    Delaet NG, Verheyden PM, Tourwe D, Van Binst G, Davis P, Burks TF.
    Biopolymers; 1992 Aug 01; 32(8):957-69. PubMed ID: 1330047
    [Abstract] [Full Text] [Related]

  • 34. Novel deltorphin heptapeptide analogs with potent delta agonist, delta antagonist, or mixed mu antagonist/delta agonist properties.
    Sasaki Y, Chiba T.
    J Med Chem; 1995 Sep 29; 38(20):3995-9. PubMed ID: 7562933
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  • 35. The opioid mu agonist/delta antagonist DIPP-NH(2)[Psi] produces a potent analgesic effect, no physical dependence, and less tolerance than morphine in rats.
    Schiller PW, Fundytus ME, Merovitz L, Weltrowska G, Nguyen TM, Lemieux C, Chung NN, Coderre TJ.
    J Med Chem; 1999 Sep 09; 42(18):3520-6. PubMed ID: 10479285
    [Abstract] [Full Text] [Related]

  • 36. Distinct conformational preferences of three cyclic beta-casomorphin-5 analogs determined using NMR spectroscopy and theoretical analysis.
    Carpenter KA, Schiller PW, Schmidt R, Wilkes BC.
    Int J Pept Protein Res; 1996 Jul 09; 48(1):102-11. PubMed ID: 8844269
    [Abstract] [Full Text] [Related]

  • 37. Structure-activity relationships of cyclic opioid peptide analogues containing a phenylalanine residue in the 3-position.
    Schiller PW, Nguyen TM, Maziak LA, Wilkes BC, Lemieux C.
    J Med Chem; 1987 Nov 09; 30(11):2094-9. PubMed ID: 2822930
    [Abstract] [Full Text] [Related]

  • 38. Dicarba analogues of the cyclic enkephalin peptides H-Tyr-c[D-Cys-Gly-Phe-D(or L)-Cys]NH(2) retain high opioid activity.
    Berezowska I, Chung NN, Lemieux C, Wilkes BC, Schiller PW.
    J Med Chem; 2007 Mar 22; 50(6):1414-7. PubMed ID: 17315860
    [Abstract] [Full Text] [Related]

  • 39. Probes for narcotic receptor-mediated phenomena. 25. Synthesis and evaluation of N-alkyl-substituted (alpha-piperazinylbenzyl)benzamides as novel, highly selective delta opioid receptor agonists.
    Katsura Y, Zhang X, Homma K, Rice KC, Calderon SN, Rothman RB, Yamamura HI, Davis P, Flippen-Anderson JL, Xu H, Becketts K, Foltz EJ, Porreca F.
    J Med Chem; 1997 Aug 29; 40(18):2936-47. PubMed ID: 9288176
    [Abstract] [Full Text] [Related]

  • 40. [2',6'-Dimethyltyrosine]dynorphin A(1-11)-NH2 analogues lacking an N-terminal amino group: potent and selective kappa opioid antagonists.
    Lu Y, Nguyen TM, Weltrowska G, Berezowska I, Lemieux C, Chung NN, Schiller PW.
    J Med Chem; 2001 Sep 13; 44(19):3048-53. PubMed ID: 11543672
    [Abstract] [Full Text] [Related]

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