GSK189254A (Synonyms: GSK189254)
目录号: PL14989 纯度: ≥98%
CAS No. :720690-73-3
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中文名称
GSK189254A
中文别名
GSK189254A
英文名称
GSK189254A
英文别名
GSK 189254A;6-[(3-cyclobutyl-1,2,4,5-tetrahydro-3-benzazepin-7-yl)oxy]-N-methylpyridine-3-carboxamide;GSK-189254;GSK-189254A;GSK189254A
Cas No.
720690-73-3
分子式
C21H25N3O2
分子量
351.44
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
GSK189254A (GSK189254)是一个新颖高效有选择性的H3受体拮抗剂,对人类和大鼠H3的pKi值分别为9.59-9.90 and 8.51-9.17。
生物活性
GSK189254A (GSK189254) is a novel, potent and selective histamine H3 receptor antagonist with pK i values of 9.59-9.90 and 8.51-9.17 for human and rat H3, respectively.
性状
Solid
IC50 & Target[1][2]
pKi: 9.59-9.90 (H3, human), 8.51-9.17 (H3, rat)
体外研究(In Vitro)
GSK189254 has high affinity for both recombinant H3 receptors expressed in HEK-293-MSR-II cells and native H3 receptors expressed in the cerebral cortex of several species. GSK189254 generally exhibits higher affinity for human and pig H3 receptors compared with rat,mouse, and dog H3 receptors. [H]GSK189254 binds in rat and human brain areas, including cortex and hippocampus. GSK189254 may have therapeutic potential for the symptomatic treatment of dementia in Alzheimer’s disease and other cognitive disorders . has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
GSK189254 (0.3-3 mg/kg p.o.) increases the release of acetylcholine, noradrenaline, and dopamine in the anterior cingulate cortex and acetylcholine in the dorsal hippocampus. GSK189254 significantly improves performance of rats in diverse cognition paradigms, including passive avoidance, water maze, object recognition, and attentional set shift. In Ox+/+ and Ox?/? mice, acute administration of GSK189254 increases W and decreases slow wave and paradoxical sleep to a similar degree to modafinil, while it reduces narcoleptic episodes in Ox?/? mice. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Medhurst AD, et al. GSK189254, a novel H3 receptor antagonist that binds to histamine H3 receptors in Alzheimers disease brain and improves cognitive performance in preclinical models. J Pharmacol Exp Ther. 2007 Jun;321(3):1032-45.
[2]. Guo RX, et al. Differential effects of acute and repeat dosing with the H3 antagonist GSK189254 on the sleep-wake cycle and narcoleptic episodes in Ox-/- mice.Br J Pharmacol. 2009 May;157(1):104-17.
溶解度数据
In Vitro: DMSO : 25 mg/mL (71.14 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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