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Fenoterol

CAS No. 13392-18-2

Fenoterol ( —— )

产品货号. M21615 CAS No. 13392-18-2

Fenoterol是β2-肾上腺素能受体的激动剂,被归类为拟交感神经β激动剂和哮喘化合物。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥503 有现货
5MG ¥723 有现货
10MG ¥1085 有现货
25MG ¥2161 有现货
50MG ¥3255 有现货
100MG 获取报价 有现货
200MG 获取报价 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
    Fenoterol
  • 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
    Fenoterol是β2-肾上腺素能受体的激动剂,被归类为拟交感神经β激动剂和哮喘化合物。
  • 产品描述
    Fenoterol is an ?agonist of ?β2-adrenergic receptor?It is classed as sympathomimetic beta agonist and asthma medication.(In Vitro):Fenoterol (1 μM; pre-incubated 30 minutes) treatment reduces AICAR-induced AMPK activation, NF-κB activation and TNF-α release, and also significantly downregulates the elevated phosphorylation levels of AMPK.Fenoterol inhibits lipopolysaccharide (LPS)-induced AMPK activation and inflammatory cytokine production in THP-1 cells.Fenoterol is also a potent exosome biogenesis and/or secretion activator in PC cells.(In Vivo):Fenoterol (0.7 mg/kg; intraperitoneal injection; twice a day; for 3 weeks) treatment suppresses mechanical allodynia during chronic treatment.
  • 体外实验
    Fenoterol (1 μM; pre-incubated 30 minutes) treatment reduces AICAR-induced AMPK activation, NF-κB activation and TNF-α release, and also significantly downregulates the elevated phosphorylation levels of AMPK.Fenoterol inhibits lipopolysaccharide (LPS)-induced AMPK activation and inflammatory cytokine production in THP-1 cells.Fenoterol is also a potent exosome biogenesis and/or secretion activator in PC cells. Western Blot Analysis Cell Line:THP-1 cells stimulated with AICAR Concentration:1 μM Incubation Time:Pre-incubated 30 minutes Result:Significantly downregulated the elevated phosphorylation levels of AMPK.
  • 体内实验
    Fenoterol (0.7 mg/kg; intraperitoneal injection; twice a day; for 3 weeks) treatment suppresses mechanical allodynia during chronic treatment. Animal Model:Male C57BL/6J mice (6 weeks old) with neuropathy Dosage:0.7 mg/kg Administration:Intraperitoneal injection; twice a day; for 3 weeks Result:Alleviated neuropathic allodynia during chronic treatment.
  • 同义词
    ——
  • 通路
    Angiogenesis
  • 靶点
    Adrenergic Receptor
  • 受体
    β2-adrenergic receptor
  • 研究领域
    Cardiovascular Disease
  • 适应症
    Congestive Heart Failure

化学信息

  • CAS Number
    13392-18-2
  • 分子量
    303.35
  • 分子式
    C17H21NO4
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:61 mg/mL (201.08 mM)
  • SMILES
    CC(Cc1ccc(O)cc1)NCC(O)c1cc(O)cc(O)c1
  • 化学全称
    5-[1-hydroxy-2-[1-(4-hydroxyphenyl)propan-2-ylamino]ethyl]benzene-13-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

1.R C Heelet al. Fenoterol: A Review of its Pharmacological Properties and Therapeutic Efficacy in Asthma[J]. Drugs 1978.
产品手册
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    Fenoterol是β2-肾上腺素能受体的激动剂,被归类为拟交感神经β激动剂和哮喘化合物。