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    齊留通,≥98%(HPLC)
    產(chǎn)品基本信息
    產(chǎn)品編號:128028
    產(chǎn)品名稱:齊留通,≥98%(HPLC)
    產(chǎn)品CAS:111406-87-2
    規(guī)格含量:20MG
    產(chǎn)品價格:2000
    聯(lián)系我們:
    產(chǎn)品詳細(xì)介紹

      齊留通,≥98%(HPLC)

      Product Name: Zileuton
      別名:ZYFLO;1-(1-(benzo[b]thiophen-2-yl)ethyl)-1-hydroxyurea
      CAS號:111406-87-2
      分子量:236.29
      介紹: Zileuton
      貯存: 儲存溫度-20°C
      可溶性:
      DMSO 47 mg/mL
      Water <1 mg/mL
      Ethanol 47 mg/mL
      生化和生理學(xué)機(jī)理:
      Description:
      IC50 Value: N/A
      zileuton(N-1(1-benzo[b]thien-2-ylethyl)-N-hydroxyurea, VIP(LA)64077) is a selective and potent 5-LO inhibitor, and thus inhibits leukotrienes (LTB4, LTC4, LTD4, and LTE4) formation.
      in vitro: Zileuton inhibited 5-hydroxyeicosatetraenoic acid synthesis by rat basophilic leukemia cell 20,000 x g supernatant and rat polymorphonuclear leukocytes (PMNL) (IC50 = 0.5 and 0.3 microM) respectively. It also inhibited leukotriene (LT)B4 biosynthesis by rat PMNL (IC50 = 0.4 microM), human PMNL (IC50 = 0.4 microM) and human whole blood (IC50 = 0.9 microM) [1]. Zileuton inhibited antigen-induced contractions of guinea-pig tracheal strips (GPTS) from actively sensitized animals with an IC50of 6 microM [1].
      in vivo: Additionally, while total tau levels were unchanged for both groups, zileuton-treated mice had a significant reduction in its phosphorylation state and insoluble forms, secondary to a decreased activation of the cdk5 kinase [2].&


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