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 |
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25MG | ¥664 | 有现货 |
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50MG | ¥1239 | 有现货 |
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100MG | ¥1790 | 有现货 |
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200MG | ¥2746 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Fenoldopam mesylate
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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
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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。
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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).
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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.
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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.
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同义词Fenoldopam, Corlopam, SK and F-82526J
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通路Others
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靶点Other Targets
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受体dopamine-1 receptor
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研究领域Cardiovascular Disease
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适应症——
化学信息
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CAS Number67227-57-0
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分子量401.86
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分子式C16H16ClNO3·CH4O3S
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 36 mg/mL 89.58 mM; H2O : 10 mg/mL24.88 mM
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SMILESCS(O)(=O)=O.OC1=CC=C(C=C1)C1CNCCC2=C(Cl)C(O)=C(O)C=C12
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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
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
产品手册
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