Flunisolide (Synonyms: 氟尼缩松)
目录号: PL05466 纯度: ≥99%
CAS No. :3385-03-3
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中文名称
Flunisolide
中文别名
氟尼缩松;6-氟-11,16Α,17,21-四羟基孕-1,4-二烯-3,20-二酮-16,17-安奈德
英文名称
Flunisolide
英文别名
Flunisolide;(6a,11b,16a)-6-Fluoro-11,21-dihydroxy-16,17-[(1-methylethylidene)bis(oxy)]-pregna-1,4-diene-3,20-dione
Cas No.
3385-03-3
分子式
C24H31O6F
分子量
434.50
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Flunisolide 是一种皮质类固醇,是具有口服活性的糖皮质激素受体 ( Glucocorticoid receptor ) 激活剂,具有抗炎活性。Flunisolide 可诱导嗜酸性粒细胞凋亡 (apoptosis),可用于哮喘或鼻炎、炎症的相关研究。
生物活性
Flunisolide is a corticosteroid, which is an orally active glucocorticoid receptor activator with anti-inflammatory activity. Flunisolide can induce eosinophil apoptosis, and is used for the research of asthma or rhinitis, and inflammation.
性状
Solid
体外研究(In Vitro)
Flunisolide (0.1-10 μM, 1 h) inhibits lung fibroblast (Isolated from lung) activation.
Flunisolide (10 μM, 24 h) reduces MMP-9, TIMP-1, TGF-β and fibronectin release by sputum cells (isolated frommild to moderate asthmatics), and induces sputum eosinophil apoptosis.
Flunisolide (0.1-10 μM μM, 24 h) effectively inhibits ICAM-1 expression and GM-CSF and IL-5 release induced by TNF-alpha in BEAS-2B cells.
Flunisolide (115 μM, 0-3 h) can be transported in a polarized way in the apical (ap) to basolateral (bl) direction in Calu-3 cells and is demonstrated to be ATP-dependent. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Flunisolide (Intranasal administration, 0.3–10 μg/mouse, daily, from days 21-27) inhibits lung inflammation, fibrosis, and airway hyper-reactivity, also improves clearance of silica particles from the lungs in silicotic mice.
Flunisolide (Intranasal administration, 0.3–10 μg/mouse, daily, from days 21-27) inhibits silica-induced macrophage and myofibroblast accumulation in the lung tissue. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Tatiana Paula Teixeira Ferreira, et al. Intranasal Flunisolide Suppresses Pathological Alterations Caused by Silica Particles in the Lungs of Mice. Front Endocrinol (Lausanne). 2020 Jun 17;11:388.
[2]. M Profita, et al. In vitro effects of flunisolide on MMP-9, TIMP-1, fibronectin, TGF-beta1 release and apoptosis in sputum cells freshly isolated from mild to moderate asthmatics. Allergy. 2004 Sep;59(9):927-32.
溶解度数据
In Vitro: DMSO : 125 mg/mL (287.69 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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