[Phe1Ψ (CH2-NH) Gly2]Nociceptin (1-13) NH2

• Description:

  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) .

• 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