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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.cn/group3/M00/3F/1D/CgoaEGbZkLWETe0AAAAAAOvKxC8707.png)
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).
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 2,310 | 待询 |
| 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). |
| 分子量 | 1367.6 |
| 分子式 | C61H102N22O14 |
| CAS No. | 213130-17-7 |
| 密度 | 1.43 g/cm3 (Predicted) |
| 存储 | 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. |
| 溶解度信息 | H2O: 0.7 mg/mL (0.51 mM), Sonication is recommended. |
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