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Journal Abstract Search

128 related items for PubMed ID: 1478783

  • 1. Novel approach to the design of synthetic radioiodinated linear V1A receptor antagonists of vasopressin.
    Manning M, Bankowski K, Barberis C, Jard S, Elands J, Chan WY.
    Int J Pept Protein Res; 1992; 40(3-4):261-7. PubMed ID: 1478783
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  • 2. Design of potent and selective linear antagonists of vasopressor (V1-receptor) responses to vasopressin.
    Manning M, Stoev S, Kolodziejczyk A, Klis WA, Kruszynski M, Misicka A, Olma A, Wo NC, Sawyer WH.
    J Med Chem; 1990 Nov; 33(11):3079-86. PubMed ID: 2231609
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  • 6. Design and synthesis of highly selective in vitro and in vivo uterine receptor antagonists of oxytocin: comparisons with Atosiban.
    Manning M, Miteva K, Pancheva S, Stoev S, Wo NC, Chan WY.
    Int J Pept Protein Res; 1995 Nov; 46(3-4):244-52. PubMed ID: 8537178
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  • 7. Design of oxytocin antagonists, which are more selective than atosiban.
    Manning M, Stoev S, Cheng LL, Wo NC, Chan WY.
    J Pept Sci; 2001 Sep; 7(9):449-65. PubMed ID: 11587184
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  • 9. Design of peptide oxytocin antagonists with strikingly higher affinities and selectivities for the human oxytocin receptor than atosiban.
    Manning M, Cheng LL, Stoev S, Wo NC, Chan WY, Szeto HH, Durroux T, Mouillac B, Barberis C.
    J Pept Sci; 2005 Oct; 11(10):593-608. PubMed ID: 15880385
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  • 10. Solid-phase synthesis of 16 potent (selective and nonselective) in vivo antagonists of oxytocin.
    Manning M, Kruszynski M, Bankowski K, Olma A, Lammek B, Cheng LL, Klis WA, Seto J, Haldar J, Sawyer WH.
    J Med Chem; 1989 Feb; 32(2):382-91. PubMed ID: 2913298
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  • 12. An investigation of position 3 in arginine vasopressin with aliphatic, aromatic, conformationally-restricted, polar and charged amino acids.
    Stoev S, Cheng LL, Olma A, Klis WA, Manning M, Sawyer WH, Wo NC, Chan WY.
    J Pept Sci; 1999 Mar; 5(3):141-53. PubMed ID: 10323558
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  • 13. Synthesis and structure-activity investigation of novel vasopressin hypotensive peptide agonists.
    Manning M, Stoev S, Cheng LL, Wo NC, Chan WY.
    J Pept Sci; 1999 Nov; 5(11):472-90. PubMed ID: 10587312
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  • 14. Synthesis and some pharmacological properties of potent and selective antagonists of the vasopressor (V1-receptor) response to arginine-vasopressin.
    Manning M, Stoev S, Bankowski K, Misicka A, Lammek B, Wo NC, Sawyer WH.
    J Med Chem; 1992 Jan 24; 35(2):382-8. PubMed ID: 1531076
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  • 16. Probing the V1a vasopressin receptor binding site with pyroglutamate-substituted linear antagonists.
    Howl J, Yarwood NJ, Stock D, Wheatley M.
    Neuropeptides; 1996 Feb 24; 30(1):73-9. PubMed ID: 8868303
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  • 17. A new series of photoactivatable and iodinatable linear vasopressin antagonists.
    Carnazzi E, Aumelas A, Barberis C, Guillon G, Seyer R.
    J Med Chem; 1994 Jun 10; 37(12):1841-9. PubMed ID: 8021923
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  • 18. Discovery and design of novel and selective vasopressin and oxytocin agonists and antagonists: the role of bioassays.
    Chan WY, Wo NC, Stoev ST, Cheng LL, Manning M.
    Exp Physiol; 2000 Mar 10; 85 Spec No():7S-18S. PubMed ID: 10795902
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  • 19. A radioiodinated linear vasopressin antagonist: a ligand with high affinity and specificity for V1a receptors.
    Schmidt A, Audigier S, Barberis C, Jard S, Manning M, Kolodziejczyk AS, Sawyer WH.
    FEBS Lett; 1991 Apr 22; 282(1):77-81. PubMed ID: 1827414
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  • 20. Isosteric substitution of Asn5 in antagonists of oxytocin and vasopressin leads to highly selective and potent oxytocin and V1a receptor antagonists: new approaches for the design of potential tocolytics for preterm labor.
    Chan WY, Wo NC, Cheng LL, Manning M.
    J Pharmacol Exp Ther; 1996 May 22; 277(2):999-1003. PubMed ID: 8627583
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