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Fenoldopam mesylate

CAS No. 67227-57-0

Fenoldopam mesylate ( Fenoldopam, Corlopam, SK and F-82526J )

产品货号. M18977 CAS No. 67227-57-0

Fenoldopam 是一种选择性多巴胺 1 受体 (DA1) 激动剂,具有利尿钠/利尿特性。它通过小动脉血管舒张来降低血压。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
10MG ¥348 有现货
25MG ¥664 有现货
50MG ¥1239 有现货
100MG ¥1790 有现货
200MG ¥2746 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Fenoldopam mesylate
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Fenoldopam 是一种选择性多巴胺 1 受体 (DA1) 激动剂,具有利尿钠/利尿特性。它通过小动脉血管舒张来降低血压。
  • 产品描述
    Fenoldopam mesylate is a synthetic benzazepine derivative which acts as a selective D1 receptor partial agonist. Fenoldopam is used as an antihypertensive agent. It was approved by the Food and Drug Administration (FDA) in September 1997. Since fenoldopam is the only intravenous agent that improves renal perfusion, in theory it could be beneficial in hypertensive patients with concomitant renal insufficiency.(In Vitro):Fenoldopam is a partial agonist with low efficacy at DA1 receptors linked to cAMP generation in the LLC-PK1 cells.Fenoldopam (0-300 μM; 48 or 72 h) displays significant antiproliferative activity against RCC cell lines.Fenoldopam (5 μM and 10 μM; 72 h) induces cell apoptosis in a dose-dependent manner.(In Vivo):Fenoldopam mesylate (subcutaneous injection; 100 mg/kg; once daily; 2 d) can induce arteritis in rats detected by magnetic resonance imaging (MRI).
  • 体外实验
    Fenoldopam is a partial agonist with low efficacy at DA1 receptors linked to cAMP generation in the LLC-PK1 cells.Fenoldopam (0-300 μM; 48 or 72 h) displays significant antiproliferative activity against RCC cell lines. Fenoldopam (5 μM and 10 μM; 72 h) induces cell apoptosis in a dose-dependent manner. Cell Proliferation Assay Cell Line:786-O, ACHN, and HK-2 cells Concentration:0-300 μM Incubation Time:48 or 72 hours Result:Inhibited the growth of ACHN cells (IC50=16.55 μM, 48 h; IC50=10.34 μM, 72 h), 786-O cells (IC50=57.89 μM, 48 h; IC50=47.52 μM, 72 h), and HK2 cells (IC50>300 μM, 48h and 72 h).Apoptosis AnalysisCell Line:ACHN cells Concentration:5 μM and 10 μM Incubation Time:72 hours Result:Increased apoptotic cells from at 2.2% (control) to 47.7% (5 μM, fenoldopam) and 60.8% (10 μM, fenoldopam), respectively.
  • 体内实验
    Fenoldopam mesylate (subcutaneous injection; 100 mg/kg; once daily; 2 d) can induce arteritis in rats detected by magnetic resonance imaging (MRI). Animal Model:Female Sprague-Dawley rats Dosage:100 mg/kg Administration:Subcutaneous injection; 100 mg/kg; once daily; 2 days Result:Showed low-intensity areas and a high signal intensity region around the artery, and these findings were considered to be erythrocytes infiltrating the arterial wall and perivascular edema, respectively.Observed perivascular edema histopathologically.
  • 同义词
    Fenoldopam, Corlopam, SK and F-82526J
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    dopamine-1 receptor
  • 研究领域
    Cardiovascular Disease
  • 适应症
    ——

化学信息

  • CAS Number
    67227-57-0
  • 分子量
    401.86
  • 分子式
    C16H16ClNO3·CH4O3S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : ≥ 36 mg/mL 89.58 mM; H2O : 10 mg/mL24.88 mM
  • SMILES
    CS(O)(=O)=O.OC1=CC=C(C=C1)C1CNCCC2=C(Cl)C(O)=C(O)C=C12
  • 化学全称
    9-chloro-5-(4-hydroxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

产品手册
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