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S89175

PF-3644022

源叶(MedMol) 98%
  • 英文名:
  • PF 3644022
  • 别名:
  • PF-3644022; PF 3644022; PF3644022
  • CAS号:
  • 1276121-88-0
  • 分子式:
  • C21H18N4OS
  • 分子量:
  • 374.46
  • 核磁/质谱:
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源叶(MedMol) S89175-5mg 98% ¥510.00元 5 - - - EA 加入购物车
源叶(MedMol) S89175-10mg 98% ¥950.00元 6 - - - EA 加入购物车
源叶(MedMol) S89175-25mg 98% ¥1640.00元 6 - - - EA 加入购物车
源叶(MedMol) S89175-100mg 98% ¥3600.00元 预计交期:2-3天 - - - EA 加入购物车
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  • 产品描述: PF-3644022 is a potent, selective, orally active and ATP-competitive MAPKAPK2 (MK2) inhibitor with an IC50 of 5.2 nM and a Ki of 3 nM. PF-3644022 also inhibits MK3 and p38 regulated/activated kinase (PRAK) with IC50s of 53 nM and 5.0 nM, respectively. PF-3644022 potently inhibits TNFα production and has anti-inflammatory effect
  • 靶点: IC50: 5.2 nM (MK2), 5.0 nM (PRAK) and 53 nM (MK3).Ki: 3 nM (MK2);p38MAPK; SerineProtease; MAPK
  • 体外研究:
    The inhibitory activity of PF-3644022 against other MAPKAP kinase family members is evaluated. Other than MNK2 with an IC50 of 148 nM, other family members are largely not inhibited, showing at least several hundred-fold selectivity versus MK2.
    In the human U937 monocytic cell line or peripheral blood mononuclear cells, PF-3644022 potently inhibits TNFα production with similar activity (IC50 of 160 nM). PF-3644022 blocks TNFα and IL-6 production in LPS-stimulated human whole blood with IC50 values of 1.6 and 10.3 μM, respectively. Inhibition of TNFα in U937 cells and blood correlates closely with inhibition of phospho-heat shock protein 27, a target biomarker of MK2 activity.
  • 体内研究:
    PF-3644022 (3-100 mg/kg; oral gavage; twice a day; for 12 days; Lewis rats) treatment shows dose-dependent inhibition of chronic paw swelling measured on day 21 after 12 days of oral dosing, with ED50 value of 20 mg/kg. Animal Model: Female Lewis rats (125-140 g) injected with streptococcal cell wall Dosage: 3 mg/kg, 10 mg/kg, 30 mg/kg, 50 mg/kg, 100 mg/kg Administration: Oral gavage; twice a day; for 12 days Result: Showed dose-dependent inhibition of chronic paw swelling measured on day 21 after 12 days of oral dosing.
  • 参考文献:
    1. Mourey RJ, et al. A benzothiophene inhibitor of mitogen-activated protein kinase-activated protein kinase 2 inhibits tumor necrosis factor alpha production and has oral anti-inflammatory efficacy in acute and chronic models of inflammation. J Pharmacol Exp Ther. 2010 Jun;333(3):797-807.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.671 ml 13.353 ml 26.705 ml
    5 mM 0.534 ml 2.671 ml 5.341 ml
    10 mM 0.267 ml 1.335 ml 2.671 ml
    50 mM 0.053 ml 0.267 ml 0.534 ml
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