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  • Pirfenidone-d5
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Pirfenidone-d5

An internal standard for the quantification of pirfenidone

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Pirfenidone-d5的二维码
  • 库存: 现货
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  • 包装
    价格
    促销价
    数量
  • 500ug
    ¥2587.00
    2070.00
    - +
  • 1mg
    ¥4100.00
    3280.00
    - +
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  • 货号: ajci64636
  • CAS: 1020719-62-3
  • 别名: 5-甲基-1-(苯基-2,3,4,5,6-D5)-2(1H)-吡啶酮,AMR69-d5
  • 分子式: C12H6D5NO
  • 分子量: 190.3
  • 纯度: >98%
  • 溶解度: Chloroform: soluble,Methanol: soluble
  • 储存: Store at -20°C
  • 库存: 现货

Background

Pirfenidone-d5 is intended for use as an internal standard for the quantification of pirfenidone by GC- or LC-MS. Pirfenidone is an orally bioavailable pyridone derivative with antifibrotic, anti-inflammatory, and antioxidant activities. It inhibits TGF-β1-stimulated increases in collagen type I, fibronectin, and Hsp47 expression in A549 lung cancer cells in a concentration-dependent manner. Pirfenidone (300 mg/kg per day) inhibits fibrosis and inhibits increases in collagen content, fibrocyte pool size, and the levels of chemokines CCL2 and CCL12 in lung in a mouse model of pulmonary fibrosis induced by bleomycin . In a mouse model of non-alcoholic steatohepatitis (NASH), pirfenidone inhibits fibrosis and increases in hepatocyte apoptosis, lobular inflammation, and hepatic expression of the fibrosis-related genes Col1a1, Timp1, Tgfb1, Pdgfb, and Fgf2 when administered at a dose of 280 mg/kg but has no effect on steatosis. Pirfenidone also inhibits NADPH-dependent lipid peroxidation in sheep liver microsomes and scavenges hydroxyl radicals (IC50s = ~6 and ~2.5 mM, respectively). Formulations containing pirfenidone have been used in the treatment of idiopathic pulmonary fibrosis.

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