[Nphe1]Nociceptin(1-13)NH2
Biological Activity
[Nphe1]Nociceptin(1-13)NH2 is a selective and competitive nociceptin receptor antagonist, devoid of any agonist activity. Binds selectively to recombinant nociceptin receptors (pKi = 8.4), and competitively antagonizes the actions of nociceptin in vitro and in vivo.Technical Data
(Modifications: Gly-1 = N-Bn-Gly, 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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Antagonistic effects of [Nphe1]nociceptin(1-13)NH2 on nociceptin receptor mediated inhibition of cAMP formation in Chinese hamster ovary cells stably expressing the recombinant human nociceptin receptor.
Hashimoto et al.
Neurosci.Lett., 2000;278:109 -
Characterization of [Nphe1]nociceptin(1-13)NH2, a new selective nociceptin receptor antagonist.
Calo et al.
Br.J.Pharmacol., 2000;129:1183 -
[Nphe1]nociceptin-(1-13)NH2 selectively antagonizes nociceptin effects in the rabbit isolated ileum.
Pheng et al.
Eur.J.Pharmacol., 2000;397:383
Product Datasheets
Citations for [Nphe1]Nociceptin(1-13)NH2
The citations listed below are publications that use Tocris products. Selected citations for [Nphe1]Nociceptin(1-13)NH2 include:
3 Citations: Showing 1 - 3
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ORL1 activation mediates a novel ORL1 receptor agonist SCH221510 analgesia in neuropathic pain in rats.
Authors: Wu & Liu
J Mol Neurosci 2018;66:10
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Bias Factor and Therapeutic Window Correlate to Predict Safer Opioid Analgesics.
Authors: Schmid Et al.
Cell 2017;171:1165
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Nociceptin/orphanin FQ decreases glutamate transmission and blocks ethanol-induced effects in the central amygdala of naive and ethanol-dependent rats.
Authors: Kallupi Et al.
Neuropsychopharmacology 2014;39:1081
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