[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2
Biological Activity
[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 is a potent agonist of the nociceptin (ORL1) receptor, demonstrated both in vitro and in vivo. Selective, competitive antagonism at the nociceptin receptor has also been reported (pA2 = 7.02 and 6.75 in the guinea pig ileum and mouse vas deferens respectively).Technical Data
(Modifications: Phe-1 - Gly-2 peptide bond replace with Psi-(CH2-NH), Lys-13 = C-terminal amide)
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Address and message sequences for the nociceptin receptor: a structure-activity study of nociceptin (1-13)-peptide amide.
Guerrini et al.
J.Med.Chem., 1997;40:1789 -
A new selective antagonist of the nociceptin receptor.
Guerrini et al.
Br.J.Pharmacol., 1998;123:163 -
Comparison of the effects of [Phe1ω(CH2-NH)Gly2-nociceptin-(1-13)NH2 in rat brain, rat vas deferens and CHO cells expressing recombinant human nociceptin receptors.
Okawa et al.
Br.J.Pharmacol., 1999;127:123 -
[Phe1ω(CH2-NH)Gly2-nociceptin-(1-13)NH2, a proposed antagonist of the nociceptin receptor, is a potent and stable agonist in the rat spinal cord.
Xu et al.
Neurosci.Lett., 1998;249:127
Product Datasheets
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Citation for [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2
The citations listed below are publications that use Tocris products. Selected citations for [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 include:
1 Citation: Showing 1 - 1
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Nociceptin inhibits cough in the guinea-pig by activation of ORL(1) receptors.
Authors: McLeod Et al.
J Biol Chem 2001;132:1175
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