BU 224 hydrochloride

Discontinued Product

0725 has been discontinued.

View all I<sub>2</sub> Receptors products.
说明: Potent, selective I2 ligand. Putative antagonist
化学名: 2-(4,5-Dihydroimidazol-2-yl)quinoline hydrochloride
说明书
引用文献 (2)
评论

生物活性 for BU 224 hydrochloride

BU 224 hydrochloride is a high affinity ligand for the imidazoline I2 binding site (Ki = 2.1 nM). Putative I2 antagonist; antagonizes the effects of imidazoline ligands on morphine antinociception. Produces ipsiversive rotational behavior in rats with a full 6-OHDA lesion of the nigrostriatal tract.

技术数据 for BU 224 hydrochloride

分子量 233.7
公式 C12H11N3.HCl
储存 Desiccate at RT
CAS Number 205437-64-5
PubChem ID 11957470
InChI Key DDFHQXAQWZWRSQ-UHFFFAOYSA-N
Smiles Cl.C1CN=C(N1)C1=NC2=CC=CC=C2C=C1

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 BU 224 hydrochloride

分析证书/产品说明书
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参考文献 for BU 224 hydrochloride

参考文献是支持产品生物活性的出版物。

Hudson et al (1999) Novel selective compounds for the investigation of imidazoline receptors. Ann.N.Y.Acad.Sci. 881 81 PMID: 10415900

MacInnes and Dut (2004) Locomotor effects of imidazoline I2-site-specific ligands and monoamine oxidase inhibitors in rats with a unilateral 6-hydroxyDA lesion of the nigrostriatal pathway. Br.J.Pharmacol. 143 952 PMID: 15545290

Sanchez-Blasquez et al (2000) Activation of I2-imidazoline receptors enhances supraspinal mor. analgesia in mice: a model to detect agonist and antagonist activities at these receptors. Br.J.Pharmacol. 130 146 PMID: 10781010

Hudson et al (1994) Affinity and selectivity of BU224 and BU239 for rabbit brain non-adrenoceptor idazoxan binding sites (I2) sites). Br.J.Pharmacol. 112 320P

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关键词: BU 224 hydrochloride, BU 224 hydrochloride supplier, Potent, selective, I2, ligand, Putative, antagonists, Imidazoline, Receptors, BU224, hydrochloride, 0725, Tocris Bioscience

2 篇 BU 224 hydrochloride 的引用文献

引用文献是使用了 Tocris 产品的出版物。 BU 224 hydrochloride 的部分引用包括:

Gründemann et al (2002) Activation of the extraneuronal monoamine transporter (EMT) from rat expressed in 293 cells. Br J Pharmacol 137 910 PMID: 12411423

Sánchez-Blázquez et al (2000) Activation of I(2)-imidazoline receptors enhances supraspinal mor. analgesia in mice: a model to detect agonist and antagonist activities at these receptors. Br J Pharmacol 130 146 PMID: 10781010


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