| 货号 | 规格 | 价格 | 上海 | 北京 | 武汉 | 南京 | 购买数量 |
|---|---|---|---|---|---|---|---|
| S81465-100mg | 99% | ￥102.00 | 8 | - | - | - |
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| S81465-250mg | 99% | ￥124.00 | 7 | - | - | - |
|
| S81465-1g | 99% | ￥355.00 | 3 | - | - | - |
|
| S81465-5g | 99% | ￥1240.00 | 1 | - | - | - |
|
Diazoxide is a benzothiadiazine derivative that is a peripheral vasodilator used for hypertensive emergencies. It lacks diuretic effect, apparently because it lacks a sulfonamide group.
| 产品描述： | Diazoxide is a benzothiadiazine derivative that is a peripheral vasodilator used for hypertensive emergencies. It lacks diuretic effect, apparently because it lacks a sulfonamide group. | ||||||||||||||||||||
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| 靶点： | ATPase;Autophagy;Potassium Channel;ATPase; PotassiumChannel; Autophagy | ||||||||||||||||||||
| 体内研究： | Diazoxide is beneficial on the improvement in cognitive tasks, reduction of anxiety, decrease in the accumulation of amyloid-beta oligomers and hyperphosphorylation of tau proteins. Diazoxide may also exerts neuroprotective effects independently of K+ channel activation by decreasing neuronal excitability and activation of N-methyl-D-aspartate (NMDA) receptors or by increasing currents trough α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors. Diazoxide-treated animals show a decrease in disease severity a few days after the first clinical signs are observed, corresponding to the acute inflammatory phase of the disease. Daily oral administration of diazoxide in EAE mice during the effector phase of the disease reduces the severity of the clinical signs without any apparent adverse effect. Diazoxide decreases demyelination and axonal loss, reduces tissue damage, inhibits microglial/macrophage and astrocytic activation and preserves neuron integrity. No effects are observed on the number of B and T lymphocytes infiltrating the spinal cord | ||||||||||||||||||||
| 细胞实验： | The phagocytic ability of microglia is determined by the uptake of 2-μm red fluorescent microspheres by BV-2 cells. Cells are treated with diazoxide 100 μM and activated with LPS/IFN-γ and then incubated with microspheres at a concentration of 0.01% for 30 min in the dark at 37°C and 5% CO2. Cells are rinsed twice in PBS solution, pelleted at 1,000 g for 5 min and resuspended in 300 μL PBS. Cells are kept on ice and analyzed by flow cytometry.(Only for Reference) | ||||||||||||||||||||
| 参考文献： | 1.Garlid KD, et al. Circ Res. 1997, 81(6):1072-1082. 2.Virgili N, et al. J Neuroinflammation. 2011, 8:149. | ||||||||||||||||||||
| 溶解性： | H2O:<1 mg/mL DMSO:43 mg/mL (186.4 mM) Ethanol:<1 mg/mL | ||||||||||||||||||||
| 保存条件： | RT | ||||||||||||||||||||
| 配置溶液浓度参考： |
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| 注意： | 部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。 |
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