[³H]UR-MK136: a highly potent and selective radi... [ChemMedChem. 2011] - PubMed

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Guanidine-acylguanidine bioisosteric approach in the design of radioligands: synthesis of a tritium-labeled N(G)-propionylargininamide ([3H]-UR-MK114) as a highly potent and selective neuropeptide Y Y1 receptor antagonist. [J Med Chem. 2008]
Guanidine-acylguanidine bioisosteric approach in the design of radioligands: synthesis of a tritium-labeled N(G)-propionylargininamide ([3H]-UR-MK114) as a highly potent and selective neuropeptide Y Y1 receptor antagonist.
Keller M, Pop N, Hutzler C, Beck-Sickinger AG, Bernhardt G, Buschauer A. J Med Chem. 2008 Dec 25; 51(24):8168-72.
Labeling of neuropeptide Y receptors in SK-N-MC cells using the novel, nonpeptide Y1 receptor-selective antagonist [3H]BIBP3226. [Eur J Pharmacol. 1995]
Labeling of neuropeptide Y receptors in SK-N-MC cells using the novel, nonpeptide Y1 receptor-selective antagonist [3H]BIBP3226.
Entzeroth M, Braunger H, Eberlein W, Engel W, Rudolf K, Wienen W, Wieland HA, Willim KD, Doods HN. Eur J Pharmacol. 1995 May 24; 278(3):239-42.
Red-fluorescent argininamide-type NPY Y1 receptor antagonists as pharmacological tools. [Bioorg Med Chem. 2011]
Red-fluorescent argininamide-type NPY Y1 receptor antagonists as pharmacological tools.
Keller M, Erdmann D, Pop N, Pluym N, Teng S, Bernhardt G, Buschauer A. Bioorg Med Chem. 2011 May 1; 19(9):2859-78. Epub 2011 Apr 12.
Review High-affinity analogues of neuropeptide Y containing conformationally restricted non-proteinogenic amino acids. [Biochem Soc Trans. 1994]
Review High-affinity analogues of neuropeptide Y containing conformationally restricted non-proteinogenic amino acids.
Beck-Sickinger AG, Hoffmann E, Paulini K, Reissig HU, Willim KD, Wieland HA, Jung G. Biochem Soc Trans. 1994 Feb; 22(1):145-9.
Review Apparent affinity and potency of BIBP3226, a non-peptide neuropeptide Y receptor antagonist, on purported neuropeptide Y Y1, Y2 and Y3 receptors. [Eur J Pharmacol. 1995]
Review Apparent affinity and potency of BIBP3226, a non-peptide neuropeptide Y receptor antagonist, on purported neuropeptide Y Y1, Y2 and Y3 receptors.
Jacques D, Cadieux A, Dumont Y, Quirion R. Eur J Pharmacol. 1995 May 4; 278(1):R3-5.

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[³H]UR-MK136: a highly potent and selective radioligand for neuropeptide Y Y₁ re...
[³H]UR-MK136: a highly potent and selective radioligand for neuropeptide Y Y₁ receptors.
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