Evidence that [Phe1 ψ(CH2 -NH)Gly2 ]nociceptin-(1-13)-NH2 , a peripheral ORL-1 receptor antagonist, acts as an agonist in the rat spinal cord
Author:
Publisher
Wiley
Subject
Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1038/sj.bjp.0702188/fullpdf
Reference11 articles.
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2. [Phe1Ψ(CH2-NH)Gly2]nociceptin-(1-13)-NH2 is an agonist of the nociceptin (ORL-1) receptor;Butor;Eur. J. Pharmacol.,1998
3. Opioid receptor subtypes in the rat spinal cord: electrophysiological evidence for a role of mu and delta opioid receptor antagonists in the control of nociception;Dickenson;Brain Res.,1987
4. A new selective antagonist of the nociceptin receptor;Guerrini;Br. J. Pharmacol,1998
5. Biochemical evidence for orphanin FQ/nociceptin receptor heterogeneity in mouse brain;Mathis;Biochem. Biophys. Res. Commun.,1997
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2. Tritium-labelled isovaleryl-RYYRIK-NH2 as potential antagonist probe for ORL1 nociceptin receptor;Bioorganic & Medicinal Chemistry;2014-11
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