[Phe1Ψ (CH2-NH) Gly2]Nociceptin (1-13) NH2
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) .
Product Specifications
Stability
≥ 2 years
Purity
>98% (HPLC)
Weight
1367.6
Molecular Formula
C61H102N22O14
Notes
Research use only, not for human use.
Receptor
——
CAS Number
213130-17-7
Available Sizes
Curated Selection
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