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Cinaciguat 99%+

货号:A108170 同义名: BAY 58-2667 产品仅供科研

Cinaciguat is the first of a class of soluble guanylate cyclase (sGC) activators in clinical development for acute decompensated heart failure.

Cinaciguat 化学结构 CAS号:329773-35-5
Cinaciguat 化学结构
CAS号:329773-35-5
Cinaciguat 3D分子结构
CAS号:329773-35-5
Cinaciguat 化学结构 CAS号:329773-35-5
Cinaciguat 3D分子结构 CAS号:329773-35-5
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Cinaciguat 纯度/质量文件

货号:A108170 标准纯度:99%+
批次查询: 批次纯度:

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Cinaciguat 生物活性

描述 Cinaciguat at 10 μM substantially boosts the production of intracellular cGMP, yet shows no dose-dependent impacts on cell contraction or calcium transient changes[2].

Cinaciguat 动物研究

Animal study Administering Cinaciguat at a dose of 10 mg/kg/day orally to diabetic rats does not alter blood glucose levels, however, it reduces water consumption. Cinaciguat treatment also mitigates oxidative stress related to diabetes mellitus, protects against alterations in the NO-sGC-cGMP-PKG pathway, and reduces myocardial hypertrophy and apoptosis associated with diabetes mellitus[1]. Cinaciguat at concentrations of 1, 10, and 100 nM elicits concentration-dependent relaxations in gastrointestinal smooth muscle strips from both WT and apo-sGC mice, although it does not affect phasic activity caused by PGF2α in these muscle strips[3].

Cinaciguat 参考文献

[1]Mátyás C, et al. The soluble guanylate cyclase activator cinaciguat prevents cardiac dysfunction in a rat model of type-1 diabetes mellitus. Cardiovasc Diabetol. 2015 Oct 31;14:145.

[2]Reinke Y, et al. The soluble guanylate cyclase stimulator riociguat and the soluble guanylate cyclase activator cinaciguat exert no direct effects on contractility and relaxation of cardiac myocytes from normal rats. Format: AbstractSend to Eur J Pharmaco

[3]Cosyns SM, et al. Influence of cinaciguat on gastrointestinal motility in apo-sGC mice. Neurogastroenterol Motil. 2014 Nov;26(11):1573-85.

Cinaciguat 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.77mL

0.35mL

0.18mL

8.84mL

1.77mL

0.88mL

17.68mL

3.54mL

1.77mL

Cinaciguat 技术信息

CAS号329773-35-5
分子式C36H39NO5
分子量565.699
别名 BAY 58-2667
运输蓝冰
存储条件

粉末 Inert atmosphere,Store in freezer, under -20°C

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 50 mg/mL(88.39 mM),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

动物实验配方
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