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- 详细信息
- 技术资料
- 保存条件:
4°C, sealed storage, away from moisture
- 英文名:
MK-870 hydrochloride dihydrate
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
17440-83-4
- 规格:
10 mM * 1 mL/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥660.0 |
|---|---|---|---|
| 规格: | 100 mg | 产品价格: | ¥600.0 |
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Amiloride hydrochloride dihydrate
CAS No. : 17440-83-4
MCE 国际站:Amiloride hydrochloride dihydrate
产品活性:Amiloride hydrochloride dihydrate (MK-870 hydrochloride dihydrate) 是上皮钠通道 (ENaC) 和尿激酶型纤溶酶原激活物受体 (uTPA) 的抑制剂。Amiloride hydrochloride dihydrate 是 polycystin-2 (PC2; TRPP2) 通道阻断剂。
研究领域:Membrane Transporter/Ion Channel | Apoptosis | Neuronal Signaling
作用靶点:Sodium Channel | Apoptosis | TRP Channel
In Vivo: Amiloride hydrochloride dihydrate is a potent epithelial sodium channels (ENaCs) blocker. Amiloride is highly concentrated in the plasma 15 to 30 minutes following the injections. 2 mg/kg dose of Amiloride hydrochloride dihydrate has no effect on blood pressure, heart rate, mesenteric vascular resistance, or hindquarters vascular resistance as compare to the baseline measurements (n=7). Over a 2 hour period, Amiloride hydrochloride dihydrate elicits negligible responses in arterial pressure (-1±1 mmHg) and heart rate (-10±6 bpm/min) as compare to baseline levels. Results show an Amiloride hydrochloride dihydrate dose-related response pattern for the c-Fos activation in the area postrema (AP). Even at the lowest dose of Amiloride hydrochloride dihydrate (0.1 mg/kg), the number of c-Fos labeled neurons in the AP is statistically different from the control rats at a p<0.01 level.
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