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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).
![[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2](https://cdn.targetmol.com/group3/M00/3F/1D/CgoaEGbZkLWETe0AAAAAAOvKxC8707.png)
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $239 | Inquiry | Inquiry |
| 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 |
| Relative Density. | 1.43 g/cm3 (Predicted) |
| Storage | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | H2O: 0.7 mg/mL (0.51 mM), Sonication is recommended. |
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