货号 | 0840/1G |
别名 | 4-(4-Chlorophenyl)-4-hydroxy-N,N-di |
是否允许进口 | 否 |
是否危险品 | 是 |
供应商 | Tocris |
生物活性 | High affinity μ-opioid receptor agonist with peripheral selectivity (Ki values are 2, 48 and 1156 nM for μ-,δ- and κ-opioid receptors respectively). Antidiarrhoeal and antihyperalgesic agent. Also a Ca2+ channel blocker; at low micromolar concentrations it blocks broad spectrum neuronal HVA Ca2+ channels and at higher concentrations it reduces Ca2+ flux through NMDA receptor operated channels. |
运输条件 | Blue Ice |
存放说明 | Ambient |
纯度 | >99 % |
计算分子量 | 513.51 |
分子式 | C29H33ClN2O2 |
可溶性/溶解性 | Soluble to 20 mM in ethanol and to 20 mM in DMSO |
参考文献 | Dehaven-Hudkinset al (1999) Loperamide (ADL 2-1294), an opioid antihyperalgesic agent with peripheral selectivity. J.Pharmacol.Exp.Ther. 289 494. PMID: 10087042. Dalyet al (1995) Maitotoxin-elicited calcium influx in cultured cells - effect of calcium channel block. Biochem.Pharmacol. 50 1187. PMID: 7488233. Churchet al (1994) Loperamide blocks high-voltage activated calcium channels and N-Methyl-D-aspartate -evoked responses in rat and mouse cultured hippocampal pyramidal neurons. Mol.Pharmacol. 45 747. PMID: 8183255. Awouterset al (1983) Pharmacology of antidiarrheal drugs. Annu.Rev.Pharmacol.Toxicol. 23 279. PMID: 6307123. |