MCE 国际站:Fenoterol (hydrobromide)
中文名:非诺特罗氢溴酸盐
CAS:1944-12-3
品牌:MedChemExpress (MCE)
存储条件:4°C, sealed storage, away from moisture
生物活性:Fenoterol hydrobromide (Th-1165a) 是一种拟交感神经药,是一种具有选择性和口服活性的 β2-adrenoceptor 激动剂。氢溴酸非诺特罗是一种有效的支气管扩张剂,可用于哮喘、支气管炎等阻塞性气道疾病相关的支气管痉挛研究[1][2]。
体外:Fenoterol(1 μM;预孵育 30 分钟)处理可降低 AICAR 诱导的 AMPK 活化、NF-κB 活化和 TNF-α 释放,还显着下调 AMPK[2] 升高的磷酸化水平。非诺特罗抑制脂多糖 (LPS) 诱导的 THP-1 细胞中 AMPK 活化和炎性细胞因子的产生[2]。非诺特罗还是一种有效的外泌体生物发生和/或分泌激活剂在 PC 细胞中[4]。
体内:非诺特罗(0.7 mg/kg;腹膜内注射;每天两次;持续 3 周)治疗可抑制慢性治疗期间的机械异常性疼痛[3]。
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研究领域:GPCR/G Protein | Neuronal Signaling
作用靶点:Adrenergic Receptor
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参考文献:[1]. Amrita Datta, et al. High-throughput screening identified selective inhibitors of exosome biogenesis and secretion: A drug repurposing strategy for advanced cancer. Sci Rep. 2018 May 25;8(1):8161.[2]. R C Heel, et al. Fenoterol: a review of its pharmacological properties and therapeutic efficacy in asthma. Drugs. 1978 Jan;15(1):3-32.[3]. Wei Wang, et al. Anti-inflammatory activities of fenoterol through β-arrestin-2 and inhibition of AMPK and NF-κB activation in AICAR-induced THP-1 cells. Biomed Pharmacother. 2016 Dec;84:185-190.[4]. Nada Choucair-Jaafar, et al. Beta2-adrenoceptor agonists alleviate neuropathic allodynia in mice after chronic treatment. Br J Pharmacol. 2009 Dec;158(7):1683-94.
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