Impentamine dihydrobromide

Discontinued Product

1858 has been discontinued.

View all Histamine H<sub>3</sub> Receptors products.
说明: Selective H3 antagonist
别名: VUF 4702
化学名: 4-(5-Aminopentyl)imidazole dihydrobromide
说明书
引用文献
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文献 (2)

生物活性 for Impentamine dihydrobromide

Impentamine dihydrobromide is a potent and highly selective histamine H3 receptor antagonist (pA2 = 8.4); displays > 30000-fold selectivity over H1 and H2 receptors. Can act as a partial agonist in SK-N-MC cells expressing human H3 receptors. Produces antinociception, possibly via a non-H1, -H2 or -H3 receptor-mediated mechanism, following central administration in vivo.

技术数据 for Impentamine dihydrobromide

分子量 315.05
公式 C8H15N3.2HBr
储存 Desiccate at RT
CAS Number 149629-70-9
PubChem ID 53439849
InChI Key QSDXAAWBBPWGEL-UHFFFAOYSA-N
Smiles Br.Br.NCCCCCC1=CN=CN1

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

产品说明书 for Impentamine dihydrobromide

参考文献 for Impentamine dihydrobromide

参考文献是支持产品生物活性的出版物。

Hough et al (1999) Antinociceptive activity of impentamine, a histamine congener, after CNS administration. Life Sci. 64 PL79 PMID: 10072195

Vollinga et al (1995) Homologs of histamine as histamine H3 receptor antagonists: a new potent and selective H3 antagonist, 4(5)-(5-aminopentyl)-1H-imidazole. J.Med.Chem. 38 266 PMID: 7830269

Wieland et al (2001) Constitutive activity of histamine H3 receptors stably expressed in SK-N-MC cells: display of agonism and inverse agonism by H3 antagonists. J.Pharmacol.Exp.Ther. 299 908 PMID: 11714875

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关键词: Impentamine dihydrobromide, Impentamine dihydrobromide supplier, Selective, H3, antagonists, Receptors, Histamine, histaminergic, VUF4702, VUF, 4702, 1858, Tocris Bioscience

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