Amiloride hydrochloride dihydrate盐酸阿米洛利二水合物,17440-83-4

Amiloride hydrochloride dihydr

ate盐酸阿米洛利二水合物,17440-83-4
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  • ¥600 - 660
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  • 美国
  • HY-B0285B
  • 2025年12月05日
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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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