Chemical Structure : NGD94-1
货号: PC-27156Not For Human Use, Lab Use Only.
NGD94-1 (NGD 94-1) is a potent and selective dopamine D4 receptor (D4R) antagonist with Ki of 3.6 nM for cloned human D4.2 receptor.
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NGD94-1 (NGD 94-1) is a potent and selective dopamine D4 receptor (D4R) antagonist with Ki of 3.6 nM for cloned human D4.2 receptor.
NGD94-1 (NGD 94-1) displays >600-fold selectivity for D4.2 receptor subtype compared with a wide variety of monoamine or other neurotransmitter receptor or modulatory sites except for 5-HT1A and 5-HT3 receptors.
NGD94-1 (NGD 94-1) is also an agonist in human embryonic kidney 293 cells expressing human recombinant dopamine D4.4 receptors.
NGD 94-1 completely reversed the decrease in forskolin-stimulated cAMP levels produced by the dopamine receptor full agonist quinpirole.
NGD94-1 (NGD 94-1) reverses subchronic phencyclidine-induced object retrieval/detour deficits in vivo.
| 分子量 | 320.40 | |
| 分子式 | C18H20N6 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
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1. J D Jentsch, et al. Psychopharmacology (Berl). 1999 Feb;142(1):78-84.
2. Gazi L, et al. Eur J Pharmacol. 1999 May 21;372(3):R9-10.
3. Tallman JF, et al. J Pharmacol Exp Ther. 1997 Aug;282(2):1011-9.
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