| 规格: | 98% |
| 分子量: | 506.5 |
| 包装 | 价格(元) |
| 1mg | 电议 |
| 5mg | 电议 |
| 10mg | 电议 |
| 25mg | 电议 |
Background:
BAN ORL 24 is an antagonist of the nociceptin (NOP) receptor (Ki= 0.24 nM in a radioligand binding assay using CHO cell membranes expressing the human receptor).1It is selective for NOP receptors over μ-, δ-, and κ-opioid receptors (Kis = 0.19, 0.34, and >1 µM, respectively). BAN ORL 24 reduces NOP-induced GTPγS binding (pA2= 9.98) and calcium mobilization (KB= 0.93 nM) in CHO cells. It inhibits electrically induced twitches in isolated mouse and rat vas deferens, as well as isolated guinea pig ileum, when used at a concentration of 100 nM. BAN ORL 24 (10 mg/kg) reverses thermal and mechanical antinociceptive activities induced by the dual agonist of µ-opioid and NOP receptors BPR1M97 in mice.2
1.Fischetti, C., Camarda, V., Rizzi, A., et al.Pharmacological characterization of the nociceptin/orphanin FQ receptor non peptide antagonist Compound 24Eur. J. Pharmacol.614(1-3)50-57(2009) 2.Chao, P.-K., Chang, H.-F., Chang, W.-T., et al.BPR1M97, a dual mu opioid receptor/nociceptin-orphanin FQ peptide receptor agonist, produces potent antinociceptive effects with safer properties than morphineNeuropharmacology166107678(2020)
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