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SD 0006

An inhibitor of p38α MAPK

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SD 0006的二维码
  • 库存: 现货
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  • 1mg
    ¥425.00
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  • 5mg
    ¥1212.00
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  • 10mg
    ¥1937.00
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  • 25mg
    ¥3412.00
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  • 50mg
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  • 货号: ajci22892
  • CAS: 271576-80-8
  • 别名: 3-[N-(2-羟基乙酰基)-4-哌啶基]-4-(4-嘧啶基)-5-(4-氯苯基)吡唑,SD-06
  • 分子式: C20H20ClN5O2
  • 分子量: 397.86
  • 纯度: >98%
  • 溶解度: DMSO : ≥ 29 mg/mL (72.89 mM)
  • 储存: Store at -20°C
  • 库存: 现货

Background

SD 0006 (SD-06) is an orally active, selective, ATP-competitive and potent diaryl pyrazole inhibitor of p38α MAP kinase, with an IC50 of 110 nM for p38α[1][2].


SD 0006 clearly inhibits p38α as shown by the dose-dependent inhibition of phosphorylation of its endogenous Hsp27 substrate[1].


SD 0006 (0-30 mg/kg) may be an effective alternative to steroids and biologics for RA therapy[1].SD0006 (3.75, 7.5 and 15 mg/kg; p.o.; b.i.d.) is highly effective in attenuating SCW-induced inflammation as shown by the dose-dependent inhibition of paw swelling[1].


参考文献:
[1]. Burnette BL, et al. SD0006: a potent, selective and orally available inhibitor of p38 kinase. Pharmacology. 2009;84(1):42-60.
[2]. Walker JK, et al. Identification of SD-0006, a potent diaryl pyrazole inhibitor of p38 MAP kinase. Bioorg Med Chem Lett. 2010 Apr 15;20(8):2634-8.

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