Chemical Structure : NS3861
货号: PC-60819Not For Human Use, Lab Use Only.
A potent, subtype-selective α3β4 nAChR partial agonist with Ki of 0.62 nM.
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A potent, subtype-selective α3β4 nAChR partial agonist with Ki of 0.62 nM; selectively activates receptors containing β4- but not β2-subunits, shows no efficacy at α4β2 receptors and only marginal efficacy at α4β4 receptors expressed in oocytes; enhances fecal pellet expulsion in a dose-dependent manner in mice that received long-term, but not short-term, morphine treatment.
分子量 | 400.29 | |
分子式 | C12H14BrNS.C4H4O4 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Harpsøe K, et al. J Biol Chem. 2013 Jan 25;288(4):2559-70.
2. Gade AR, et al. J Pharmacol Exp Ther. 2016 Jun;357(3):520-8.
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