[Phe1Ψ (CH2-NH) Gly2]Nociceptin (1-13) NH2
This compound is a potent and selective nociceptin (ORL1) receptor agonist, as confirmed in both in vitro and in vivo studies. It also acts as a competitive antagonist in specific bioassays, such as the guinea pig ileum and mouse vas deferens. This dual activity makes it a valuable research tool for studying pain, addiction, and anxiety pathways.
Product Specifications
Field of Research
Metabolism Research, Neuroscience, Pharmacology & Drug Discovery
Molecular Weight
1367.6
Storage Conditions
-20°C
Notes
For research use only.
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