产品描述
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).
Cas No.
213130-17-7
分子式
C61H102N22O14
分子量
1367.6
别名
[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2
储存和溶解度
H2O:0.70 mg/mL
Powder: -20°C for 3 years
In solvent: -80°C for 2 years