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Fenoterol hydrobromide (Th-1165a) 是拟交感神经剂,是一种选择性的,具有口服活性 β2-肾上腺素受体 (β2-adrenoceptor) 激动剂。Fenoterol hydrobromide 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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更新时间:2026/10/7 8:40:44关注度:2464
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CAS No. : 1944-12-3
MCE 国际站:Fenoterol hydrobromide
产品活性:Fenoterol hydrobromide (Th-1165a) 是拟交感神经剂,是一种选择性的,具有口服活性 β2-肾上腺素受体 (β2-adrenoceptor) 激动剂。Fenoterol hydrobromide 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。
研究领域:GPCR/G Protein | Neuronal Signaling
作用靶点:Adrenergic Receptor
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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