
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)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥503 | 有现货 |
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5MG | ¥723 | 有现货 |
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10MG | ¥1085 | 有现货 |
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25MG | ¥2161 | 有现货 |
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50MG | ¥3255 | 有现货 |
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100MG | 获取报价 | 有现货 |
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200MG | 获取报价 | 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Fenoterol
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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。
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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.
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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.
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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.
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同义词——
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通路Angiogenesis
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靶点Adrenergic Receptor
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受体β2-adrenergic receptor
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研究领域Cardiovascular Disease
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适应症Congestive Heart Failure
化学信息
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CAS Number13392-18-2
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分子量303.35
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分子式C17H21NO4
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纯度>98% (HPLC)
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溶解度DMSO:61 mg/mL (201.08 mM)
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SMILESCC(Cc1ccc(O)cc1)NCC(O)c1cc(O)cc(O)c1
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化学全称5-[1-hydroxy-2-[1-(4-hydroxyphenyl)propan-2-ylamino]ethyl]benzene-13-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
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
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。