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Journal Abstract Search

481 related items for PubMed ID: 15787962

  • 1. Structure-activity relationships of arodyn, a novel acetylated kappa opioid receptor antagonist.
    Bennett MA, Murray TF, Aldrich JV.
    J Pept Res; 2005 Mar; 65(3):322-32. PubMed ID: 15787962
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  • 2. Synthesis and opioid activity of side-chain-to-side-chain cyclic dynorphin A-(1-11) amide analogues cyclized between positions 2 and 5. 1. Substitutions in position 3.
    Vig BS, Murray TF, Aldrich JV.
    J Med Chem; 2004 Jan 15; 47(2):446-55. PubMed ID: 14711314
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  • 3. Effects of the substitution of Phe4 in the opioid peptide [D-Ala8]dynorphin A-(1-11)NH2.
    Vig BS, Zheng MQ, Murray TF, Aldrich JV.
    J Med Chem; 2003 Sep 11; 46(19):4002-8. PubMed ID: 12954053
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  • 5. [Nalpha-benzylTyr1,cyclo(D-Asp5,Dap8)]- dynorphin A-(1-11)NH2 cyclized in the "address" domain is a novel kappa-opioid receptor antagonist.
    Patkar KA, Yan X, Murray TF, Aldrich JV.
    J Med Chem; 2005 Jul 14; 48(14):4500-3. PubMed ID: 15999987
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  • 7. Identification of arodyn, a novel acetylated dynorphin A-(1-11) analogue, as a kappa opioid receptor antagonist.
    Bennett MA, Murray TF, Aldrich JV.
    J Med Chem; 2002 Dec 19; 45(26):5617-9. PubMed ID: 12477343
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  • 8. Design, synthesis, and opioid activity of arodyn analogs cyclized by ring-closing metathesis involving Tyr(allyl).
    Fang WJ, Murray TF, Aldrich JV.
    Bioorg Med Chem; 2018 Mar 15; 26(6):1157-1161. PubMed ID: 29273415
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  • 10. Novel diastereomeric opioid tetrapeptides exhibit differing pharmacological activity profiles.
    Ioja E, Tourwé D, Kertész I, Tóth G, Borsodi A, Benyhe S.
    Brain Res Bull; 2007 Sep 14; 74(1-3):119-29. PubMed ID: 17683797
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  • 13. Development of highly potent and selective dynorphin A analogues as new medicines.
    Lung FD, Chen CH, Liu JH.
    J Pept Res; 2005 Nov 14; 66(5):263-76. PubMed ID: 16218994
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  • 17. Design, synthesis, and biological activities of cyclic lactam peptide analogues of dynorphine A(1-11)-NH2.
    Lung FD, Collins N, Stropova D, Davis P, Yamamura HI, Porreca F, Hruby VJ.
    J Med Chem; 1996 Mar 01; 39(5):1136-41. PubMed ID: 8676350
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  • 18. Design of potent and selective agonists for the human vasopressin V1b receptor based on modifications of [deamino-cys1]arginine vasopressin at position 4.
    Cheng LL, Stoev S, Manning M, Derick S, Pena A, Mimoun MB, Guillon G.
    J Med Chem; 2004 Apr 22; 47(9):2375-88. PubMed ID: 15084136
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  • 19. Structure-activity relationships of dynorphin analogs substituted in positions 2 and 3.
    Schlechtingen G, DeHaven RN, Daubert JD, Cassel J, Goodman M.
    Biopolymers; 2003 Apr 22; 71(1):71-6. PubMed ID: 12712501
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  • 20. Direct influence of C-terminally substituted amino acids in the Dmt-Tic pharmacophore on delta-opioid receptor selectivity and antagonism.
    Balboni G, Salvadori S, Guerrini R, Negri L, Giannini E, Bryant SD, Jinsmaa Y, Lazarus LH.
    J Med Chem; 2004 Jul 29; 47(16):4066-71. PubMed ID: 15267245
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