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莫索尼定 /Moxonidine {[allProObj[0].p_purity_real_show]}

货号:A482917 同义名: 莫索尼啶 / BDF5895;LY326869

Moxonidine是一种选择性的咪唑啉 I1 受体激动剂和 α-2 受体激动剂,主要用于抗高血压治疗。

Moxonidine 化学结构 CAS号:75438-57-2
Moxonidine 化学结构
CAS号:75438-57-2
Moxonidine 3D分子结构
CAS号:75438-57-2
Moxonidine 化学结构 CAS号:75438-57-2
Moxonidine 3D分子结构 CAS号:75438-57-2
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Moxonidine 纯度/质量文件 产品仅供科研

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Moxonidine 生物活性

描述 Moxonidine is a selective agonist at the imidazoline receptor subtype 1 with very weak binding affinity for α2-adrenoceptors, used as antihypertensive agent[3]. Hypotensive and bradycardic actions of moxonidine but not clonidine are mediated through imidazoline receptors and are dependent on intact noradrenergic pathways within the RVLM(rostral ventrolateral medulla)[4]. Moxonidine binds with an affinity for the imidazoline I1 receptor that is 33 times more effective than is alpha2-receptor binding. There is a regression of left-ventricular hypertrophy after moxonidine was given for 6 months. Following oral administration the half-life (Tmax) is about 1 h. Moxonidine is highly bioavailable, approaching 90%[5]. Moreover, moxonidine (10 μmol·L-1) significantly inhibited the frequency of spontaneous EPSCs in both inspiratory-activated and inspiratory-inhibited AVPNs (airway vagal preganglionic neurons). Thus moxonidine inhibits the excitatory inputs to AVPNs via activation of both α2-adrenoceptors and imidazoline I1 receptors, and suggest that physiologically both of these two types of receptors are involved in the central regulation of airway vagal activity at preganglionic level[6].

Moxonidine 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT02614794 HER2 Positive Breast Cancer Phase 2 Recruiting July 2021 -
NCT03622905 Alzheimer Disease Not Applicable Not yet recruiting October 1, 2024 -
NCT02574455 Breast Cancer Phase 3 Recruiting June 2020 -

Moxonidine 参考文献

[1]Alves TB, Totola LT, et al. GABA mechanisms of the nucleus of the solitary tract regulates the cardiovascular and sympathetic effects of moxonidine. Auton Neurosci. 2016 Jan;194:1-7.

[2]Gasparini S, Menani JV, et al. Moxonidine into the lateral parabrachial nucleus modifies postingestive signals involved in sodium intake control. Neuroscience. 2015 Jan 22;284:768-74.

[3]Schäfer U, Burgdorf C, Engelhardt A, Kurz T, Richardt G. Presynaptic effects of moxonidine in isolated buffer perfused rat hearts: role of imidazoline-1 receptors and alpha2-adrenoceptors. J Pharmacol Exp Ther. 2002 Dec;303(3):1163-70

[4]Chan CK, Burke SL, Zhu H, Piletz JE, Head GA. Imidazoline receptors associated with noradrenergic terminals in the rostral ventrolateral medulla mediate the hypotensive responses of moxonidine but not clonidine. Neuroscience. 2005;132(4):991-1007

[5]Prichard BN, Graham BR, Owens CW. Moxonidine: a new antiadrenergic antihypertensive agent. J Hypertens Suppl. 1999 Aug;17(3):S41-54

[6]Zhou X, He D, Yan X, Chen X, Li R, Zhang G, Wang J. Moxonidine inhibits excitatory inputs to airway vagal preganglionic neurons via activation of both α2-adrenoceptors and imidazoline I1 receptors. Brain Res. 2020 Apr 1;1732:146695

Moxonidine 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.14mL

0.83mL

0.41mL

20.69mL

4.14mL

2.07mL

41.38mL

8.28mL

4.14mL

Moxonidine 技术信息

CAS号75438-57-2
分子式C9H12ClN5O
分子量 241.678
别名 莫索尼啶 ;BDF5895;LY326869
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Keep in dark place,Inert atmosphere,2-8°C

溶解方案

DMSO: 18 mg/mL(74.48 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案一
方案二
动物实验配方
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