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GSNOR-IN-1 是 GSNOR-IN-2 的前体药物,是一种能够穿透血脑屏障的 S-亚硝基谷胱甘肽还原酶 (GSNOR) 抑制剂。其对氧糖剥夺/复氧 (OGD/R) 诱导的损伤有着显著的保护效果。GSNOR-IN-1 通过调节 Clstn1 的 S-亚硝化,来影响钙信号传导和突触功能,并抑制神经元凋亡 (apoptosis)。在缺血性中风大鼠模型中,GSNOR-IN-1 能显著减少梗死体积,并改善神经功能缺损,展现了其在神经保护和缺血性中风研究中的潜力。
GSNOR-IN-1 是 GSNOR-IN-2 的前体药物,是一种能够穿透血脑屏障的 S-亚硝基谷胱甘肽还原酶 (GSNOR) 抑制剂。其对氧糖剥夺/复氧 (OGD/R) 诱导的损伤有着显著的保护效果。GSNOR-IN-1 通过调节 Clstn1 的 S-亚硝化,来影响钙信号传导和突触功能,并抑制神经元凋亡 (apoptosis)。在缺血性中风大鼠模型中,GSNOR-IN-1 能显著减少梗死体积,并改善神经功能缺损,展现了其在神经保护和缺血性中风研究中的潜力。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
GSNOR-IN-1 相关产品
| 产品描述 | GSNOR-IN-1 is a prodrug of GSNOR-IN-2 and functions as an S-nitrosoglutathione reductase (GSNOR) inhibitor capable of crossing the blood-brain barrier. GSNOR-IN-1 offers significant protective effects against damage induced by oxygen-glucose deprivation/reoxygenation (OGD/R). It regulates calcium signaling and synaptic function through Clstn1 S-nitrosylation and inhibits neuronal apoptosis. Additionally, GSNOR-IN-1 markedly reduces infarct volume in rat models of ischemic stroke while enhancing neurological function. With its neuroprotective properties, GSNOR-IN-1 holds potential for ischemic stroke research. |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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