1. Academic Validation
  2. GR159897, a potent non-peptide antagonist at tachykinin NK2 receptors

GR159897, a potent non-peptide antagonist at tachykinin NK2 receptors

  • Eur J Pharmacol. 1995 Jan 16;272(2-3):241-8. doi: 10.1016/0014-2999(94)00655-q.
I J Beresford 1 R L Sheldrick D I Ball M P Turpin D M Walsh A B Hawcock R A Coleman R M Hagan M B Tyers
Affiliations

Affiliation

  • 1 Department of Pharmacology, Glaxo Research and Development Ltd, Ware, Herts., UK.
Abstract

GR159897 ((R)-1-[2-(5-fluoro-1H-indol-3-yl)ethyl]-4-methoxy-4- [(phenylsulfinyl)methyl]piperidine) is a novel, highly potent and selective non-peptide antagonist at tachykinin NK2 receptors. GR159897 inhibited binding of the NK2 receptor antagonist radioligand [3H]cyclohexylcarbonyl-Gly-Ala-(D)Trp-Phe-NMe2 ([3H]GR100679) to human ileum NK2 receptors transfected into Chinese hamster ovary cells (pKi 9.5) and to rat colon membranes (pKi 10.0). GR159897 was a competitive antagonist of contractions induced by the NK2 receptor agonist [Lys3,Gly8-R-gamma-lactam-Leu9]neurokinin A-(3-10) (GR64349) in guinea-pig trachea (pA2 8.7), and had negligible activity at human NK1 receptors transfected into Chinese hamster ovary cells (pKi 5.3), NK1 receptors in guinea-pig trachea (pKB < 5) or NK3 receptors in guinea-pig cerebral cortex (pKi < 5). In vivo, in the anaesthetised guinea-pig, GR159897 (0.12 mg.kg-1 i.v.) potently antagonised bronchoconstriction induced by GR64349 (dose-ratio = 28), with a long duration of action (3 h). GR159897 should be a useful tool for studying the physiological and pathophysiological role of tachykinin NK2 receptor activation.

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