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JNJ-42041935,HIF-PHDInhibitor M60285-2s|产品详情|进口橙子视频旧款采购网




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    上海橙子视频app安卓下载生物科技公司
    Tel:400-968-7988    021-33779008
    JNJ-42041935,HIF-PHDInhibitor
    品牌:Xcessbio
    货号:M60285-2s
    规格:2 mg solid
    货期:

    JNJ-42041935,HIF-PHDInhibitor

    商品详情 参考文献 相关资料
    Product Information
    Molecular Weight: 346.65
    Formula: C12H6ClF3N4O3
    Purity: ≥98%
    CAS#: 1193383-09-3
    Solubility: DMSO up to 100 mM
    Chemical Name: 1-(5-chloro-6-(trifluoromethoxy)-1H-benzo[d]imidazol-2-yl)-1H-pyrazole-4-carboxylic acid
    Storage: Powder: 4oC 1 year. DMSO: 4oC 3 month; -20oC 1 year.

    Biological Activity:

    JNJ-42041935 is a potent and selective HIF-PHD inhibitor. It is a 2-OG competitive and reversible inhibitor for PHD enzymes (pKis = 7.91, 7.29, and 7.65 for PHD1, 2, and 3, respectively). It is >100-fold selective for PHD compared to the related FIH (factor-inhibiting HIF) and a panel of various other enzymes. In an inflammation-induced anemia model in rats, 100 µM/kg/day JNJ-42041935 significantly increased the number of circulating reticulocytes and red blood cells, increased blood hemoglobin and hematocrit, and restored mean corpuscular volume and mean cell hemoglobin of red bloods cells. JNJ-42041935 is a new pharmacological tool, which can be used to investigate PHD inhibition and demonstrate that PHD inhibitors offer great promise for the treatment of inflammation-induced anemia.

    How to Use:

    In vitro:
    JNJ-42041935 was used at 10 µM final concentration in vitro and in cellular assays.
    In vivo: JNJ-42041935 was dosed to mice orally at 100 µM/kg once per day. 


    Reference:
    • 1. Barrett TD, et al. Pharmacological characterization of 1-(5-chloro-6-(trifluoromethoxy)-1H-benzoimidazol-2-yl)-1H-pyrazole-4-carboxylic acid (JNJ-42041935), a potent and selective hypoxia-inducible factor prolyl hydroxylase inhibitor. (2011) Mol Pharmacol. 79(6):910-20. 


     
         


    Products are for research use only. Not for human use. 

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