目錄:MedChemExpress LLC>>生化試劑>> Budesonide | MCE
參考價(jià) | ¥ 465 |
參考價(jià) | ¥ 465 |
更新時(shí)間:2023-06-15 09:27:10瀏覽次數(shù):168評(píng)價(jià)
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CAS | 51333-22-3 | 純度 | 99.94% |
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分子量 | 430.53 | 分子式 | C??H??O? |
供貨周期 | 現(xiàn)貨 | 規(guī)格 | 100 mg |
貨號(hào) | HY-13580 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 51333-22-3
產(chǎn)品活性:Budesonide, an inhaled glucocortical steroid, is an orally active glucocorticoid receptor agonist. Budesonide decreases the size of lung tumors, reverses DNA hypomethylation and modulates mRNA expression of genes. Budesonide is an anti-inflammatory agent used for asthma.
研究領(lǐng)域:Immunology/Inflammation | Vitamin D Related/Nuclear Receptor
作用靶點(diǎn):Glucocorticoid Receptor
In Vitro: Budesonide is selective for human glucocorticoid receptor (hGR; EC50=45.7 pM) over mineralocorticoid receptors (EC50=7,620 pM) in CV-1 cells.
Budesonide (30?min prior to LPS) suppresses the activation of the NLRP3 inflammasome by LPS (100?ng/mL) plus ATP (5?mM) in macrophages (RAW 264.7 cells).
In Vivo: Budesonide (2.0 mg/kg; orally via their diet; at 2, 7 and 21 days prior to killing) decreases the size of lung tumors.
Budesonide (0.5?mg/kg; intranasal administration 1?h before LPS injection (5?mg/kg)) pretreatment dramatically attenuates pathological injury and reduces pathological scores in mice with ALI in adult male C57BL/6 mice.
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