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Mirodenafil dihydrochloride

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  • ¥500 - 3840
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-14930A
  • 2025年07月13日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      4°C, stored under nitrogen

    • 英文名

      SK-3530 dihydrochloride

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • 规格

      10 mM * 1 mL/5 mg/10 mg/50 mg/100 mg

    规格:10 mM * 1 mL产品价格:¥665.0
    规格:5 mg产品价格:¥500.0
    规格:10 mg产品价格:¥800.0
    规格:50 mg产品价格:¥2400.0
    规格:100 mg产品价格:¥3840.0

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    Mirodenafil dihydrochloride

    CAS No. : 862189-96-6

    MCE 国际站:Mirodenafil dihydrochloride

    产品活性:Mirodenafil (SK3530) dihydrochloride 是一种口服有效、可逆的、选择性的磷酸二酯酶 5 (PDE5) 的抑制剂。Mirodenafil dihydrochloride 是一种糖皮质激素受体 (GR) 的调节剂。Mirodenafil dihydrochloride 通过下调 Dkk1 的表达,激活 Wnt/β-catenin 信号通路。Mirodenafil dihydrochloride 可用于研究勃起功能障碍 (ED)、阿尔茨海默病 (AD) 和系统性硬化症 (SSc)。

    研究领域:Metabolic Enzyme/Protease  |  Vitamin D Related/Nuclear Receptor  |  Immunology/Inflammation  |  Stem Cell/Wnt  |  Apoptosis

    作用靶点:Phosphodiesterase (PDE)  |  Glucocorticoid Receptor  |  Wnt  |  β-catenin  |  Apoptosis

    In Vitro: Mirodenafil dihydrochloride (0-40 μM, 24 h) exerts neuroprotective functions via activating the cGMP/PKG/CREB signaling pathway.
    Mirodenafil dihydrochloride (0-40 μM, 24 h) enhances neuronal survival by protecting the mitochondrial membrane potential and inhibiting apoptosis.
    Mirodenafil dihydrochloride (0-40 μM) inhibits GSK-3β signaling, resulting in reduced tau phosphorylation, decreased Aβ production by inhibiting amyloidogenesis and activating the autophagosomal pathway.
    Mirodenafil dihydrochloride inhibits the transcriptional activity of the glucocorticoid receptor (GR), and inhibits homodimerization of GR in HT-22 cells.
    Mirodenafil dihydrochloride (0-100 μM, 24 h) inhibits TGF-β-induced phosphorylation of Smad2/3 and mRNA expression of the fibrosis marker in fibroblasts.

    In Vivo: Mirodenafil dihydrochloride (4 mg/kg, IP, daily for 4 weeks) enhances the cognitive-behavioral performance in transgenic AD mice.
    Mirodenafil dihydrochloride (0-10 mg/kg, Orally, daily for 3 weeks) ameliorates dermal fibrosis in a BLM-induced SSc mouse model by inhibiting the TGF-β signaling pathway, thereby suppressing the expression of collagen and profibrotic genes.

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    图标文献和实验
    相关实验
    • 疟原虫 Malaria Parasites(Plasmodium)

      can be used:Quinine dihydrochloride 20 mg salt/kg base given I.V. in 5% w/v dextrose or normal saline as a once-only 4 hour infusion followed, 4 hours later, by quinine dihydrochloride 10 mg salt/kg base 4-hour infusions 8 hourly.Where a syringe pump

    • Measuring Antioxidant Capacity Using the ORAC and TOSC Assays

      by antioxidants, and the second is the total oxyradical scavenging capacity (TOSC) assay, which measures the decrease in ethylene gas production caused by the inhibition of the thermal hydrolysis of ABAP (2,2′-Azobis(2-methyl-(propionamidine) dihydrochloride

    • 用DAPI进行细胞染色

      for each d12 mm coverslip, 25 µl for square coverslip and 50µl for full size coverslip• Seal the coverslip with nail polish• Store in 4 C up to 2 weeksDAPI stock• 4’, 6-Diamidino-2-phenylindole dihydrochloride hydrate (DAPI) from Sigma (Cat# D-9542), 1 mg 1mg

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