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S87917

BN82002 HYDROCHLORIDE SALT

源叶(MedMol) 98%
  • 英文名:
  • BN82002 HYDROCHLORIDE SALT
  • 别名:
  • CAS号:
  • 396073-89-5
  • 分子式:
  • C19H25N3O4.ClH
  • 分子量:
  • 395.884
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源叶(MedMol) S87917-1mg 98% ¥380.00元 预计交期:2-3天 - - - EA 加入购物车
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  • 产品描述: BN82002 hydrochloride is a potent, selective and irreversible inhibitor of CDC25 phosphatase family. BN82002 hydrochloride inhibits CDC25A, CDC25B2, CDC25B3, CDC25C CDC25A, and 25C-cat with IC50 values of 2.4, 3.9, 6.3, 5.4, and 4.6 µM, respectively. BN82002 hydrochloride displays ~20-fold greater selectivity over CD45 tyrosine phosphatase
  • 靶点: IC50: 2.4 μM (CDC25A), 3.9 μM (CDC25B2), 6.3 μM (CDC25B3), 5.4 μM (CDC25C), 4.6 μM (CDC25C-cat);Phosphatase
  • 体外研究:
    The effect of BN82002 on cell proliferation is evaluated in vitro on several human tumor cell lines. Menadione, which has been reported to inhibit cell proliferation, is used as a control. All of the examined cell lines are sensitive to BN82002 and Menadione in a concentration-dependent manner in the low micromolar range. The most sensitive is the pancreatic cancer cell line MIA PaCa-2 with an IC50 of 7.2 μM, and the less sensitive cell line is the colon cancer HT-29 with an IC50 of 32.6 μM. The range of activity is very similar to the one observed with menadione (5-15 μM). It is also showed that 50 μM BN82002 is a concentration that fully inhibits cell proliferation, the cell cycle distribution is only modestly affected with a slight decrease in S phase and an increase in cells containing both a G1 and a G2 DNA content, suggesting that the cells treated with BN82002 are arrested at various stages of the cell cycle
  • 参考文献:
    1. Brezak MC, et al. A novel synthetic inhibitor of CDC25 phosphatases: BN82002. Cancer Res. 2004 May 1;64(9):3320-5.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: 2-8°C
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.526 ml 12.63 ml 25.26 ml
    5 mM 0.505 ml 2.526 ml 5.052 ml
    10 mM 0.253 ml 1.263 ml 2.526 ml
    50 mM 0.051 ml 0.253 ml 0.505 ml
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