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首页-小分子抑制剂&激动剂-GPCR-Histamine Receptor-GSK189254
GSK189254

Chemical Structure : GSK189254

CAS No.: 945493-87-8

GSK189254 (GSK189254A hydrochloride)

货号: PC-27477Not For Human Use, Lab Use Only.

GSK189254 (GSK189254A hydrochloride) is a potent, selective histamine H3 receptor (H3R) antagonist with pKi of 9.59 -9.90 and 8.51-9.17 for human and rat H3R respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

GSK189254 (GSK189254A hydrochloride) is a potent, selective histamine H3 receptor (H3R) antagonist with pKi of 9.59 -9.90 and 8.51-9.17 for human and rat H3R respectively.
GSK189254 exhibits potent functional antagonism (pA(2) = 9.06 versus agonist-induced changes in cAMP) and inverse agonism [pIC(50) = 8.20 versus basal guanosine 5'-O-(3-[(35)S]thio)triphosphate binding] at the human recombinant H(3) receptor.
GSK189254 inhibits cortical ex vivo R-(-)-alpha-methyl[imidazole-2,5(n)-(3)H]histamine dihydrochloride ([(3)H]R-alpha-methylhistamine) binding (ED(50) = 0.17 mg/kg) and increases c-Fos immunoreactivity in prefrontal and somatosensory cortex (3 mg/kg).
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 (1 and 3 mg/kg p.o.), water maze (1 and 3 mg/kg p.o.), object recognition (0.3 and 1 mg/kg p.o.), and attentional set shift (1 mg/kg p.o.).

物理化学性质&存储条件

分子量 387.91
分子式 C21H26ClN3O2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

6-[(3-Cyclobutyl-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl)oxy]-N-methyl-3-pyridinecarboxamide hydrochloride

参考文献

1. Giannoni P, et al. J Pharmacol Exp Ther. 2010 Jan;332(1):164-72.

2. Guo RX, et al. Br J Pharmacol. 2009 May;157(1):104-17.

3. Medhurst AD, et al. J Pharmacol Exp Ther. 2007 Jun;321(3):1032-45.

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