keep away from moisture
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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).
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
1 mg | Inquiry | $ 239.00 |
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). |
Molecular Weight | 1367.6 |
Formula | C61H102N22O14 |
CAS No. | 213130-17-7 |
keep away from moisture
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 0.70 mg/mL
You can also refer to dose conversion for different animals. More
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[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 213130-17-7 [Phe1Ψ(CH2-NH)Gly2]NociceptinNH2 [Phe1Ψ(CH2 NH)Gly2]Nociceptin(1 13)NH2 [Phe1psi(CH2-NH)Gly2]NociceptinNH2 [Phe1Ψ(CH2NH)Gly2]Nociceptin(113)NH2 [Phe-1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 inhibitor inhibit