中文名称: | 非诺特罗 | ||||
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英文名称: | Fenoterol | ||||
别名: | 非诺特罗 Th-1165; Phenoterol | ||||
CAS No: | 13392-18-2 | 分子式: | C17H21NO4 | 分子量: | 303.35 |
CAS No: | 13392-18-2 | ||||
分子式: | C17H21NO4 | ||||
分子量: | 303.35 |
基本信息
产品编号: |
F10341 |
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产品名称: |
Fenoterol |
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CAS: |
13392-18-2 |
储存条件 |
粉末 |
-20℃ |
四年 |
分子式: |
溶于液体 |
-80℃ |
二年 |
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分子量: |
303.35 |
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化学名: |
1-(3,5-Dihydroxyphenyl)-1-hydroxy-2-((4-hydroxyphenyl)isopropylamino)ethane |
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Solubility (25°C): |
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体外:
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DMSO |
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Ethanol |
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Water |
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体内(现配现用): |
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<1mg/ml表示微溶或不溶。 |
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普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。 |
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;⼀旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |
生物活性
产品描述 |
一种选择性的,具有口服活性 β2-肾上腺素受体 (β2-adrenoceptor) 激动剂。Fenoterol 是一种有效的支气管扩张剂,可用于与哮喘,支气管炎和其他阻塞性气道疾病相关的支气管痉挛的研究。 |
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靶点 |
Adrenergic Receptor |
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体外研究 |
Fenoterol (1μM;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 |
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Cell Line: |
THP-1 cells stimulated with AICAR |
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Concentration: |
1μM |
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Incubation Time: |
Pre-incubated 30 minutes |
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Result: |
Significantly downregulated the elevated phosphorylation levels of AMPK. |
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体内研究 |
Fenoterol (0.7mg/kg;intraperitoneal injection;twice a day;for 3 weeks) treatment suppresses mechanical allodynia during chronic treatment. |
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Animal Model: |
Male C57BL/6J mice (6 weeks old) with neuropathy |
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Dosage: |
0.7mg/kg |
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Administration: |
Intraperitoneal injection;twice a day;for 3 weeks |
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Result: |
Alleviated neuropathic allodynia during chronic treatment. |
本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系,公式为:
质量 (g) = 浓度 (mol/L) x 体积 (L) x 分子量 (g/mol)
摩尔浓度计算公式
用本工具协助配置特定浓度的溶液,使用的计算公式为:
开始浓度 x 开始体积 = 最终浓度 x 最终体积
稀释公式
稀释公式一般简略地表示为:C1V1 = C2V2 ( 输入 输出 )