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5(S),6(R)-7-trihydroxymethyl Heptanoate

产品信息
  • 规格: 1mg 产品价格: ¥585.0
    规格: 5mg 产品价格: ¥2639.0
    规格: 10mg 产品价格: ¥4680.0

    产品说明YZ白三烯B4(LTB4)诱导的多形核嗜中性粒细胞(PMN)趋化性
    该产品包含在以下化合物库中:
      质量控制
      • 纯度 = 98.00%
      化学性质
      CAS号 78606-80-1    
      别名 BML-111
      分子式 C8H16O5 分子量 192.2
      溶解性 Soluble in DMSO 储存条件 Store at -20°
       实验操作
      细胞实验[2]:

      细胞系

      溶解方法

      反应时间

      应用

      动物实验[3]:

      动物模型

      剂量

      注意事项

      References:

      产品描述

      5(S), 6(R)-7-trihydroxymethyl Heptanoate is a C-7 truncated analog of lipoxin A4 (LXA4). 5(S), 6(R)-7-trihydroxymethyl Heptanoate shows an inhibitory effect on leukotriene B4 (LTB4)-induced polymorphonuclear neutrophils (PMN) chemotaxis [1].

      Lipoxins (LXs) are trihydroxy tetraene metabolites endogenously produced anti-inflammatory eicosanoids [2]. Lipoxins were derived from arachidonic acid through an interaction between different lipoxygenases with carbon-15 and carbon-5 to form LXA 4 and LXB 4 [1]. LXs functioned as endogenous “braking signals” in inflammation [2]. LXs showed diverse bioactions on individual leukocytes, stimulating the activation of monocytes and macrophages, inhibiting the activation of PMNs, eosinophils, and lymphocytes [2].

      5(S),6(R)-7-trihydroxymethyl Heptanoate inhibited leukotriene B4 (LTB4)-induced polymorphonuclear neutrophils (PMN) chemotaxis with an IC50 value of 5 nM, which was equiactive as LXA4 [1].

      References:
      [1] Lee T H, Lympany P, Crea A E G, et al.  Inhibition of leukotriene B 4-induced neutrophil migration by lipoxin A 4: structure-function relationships[J]. Biochemical and biophysical research communications, 1991, 180(3): 1416-1421.
      [2] McMahon B, Godson C.  Lipoxins: endogenous regulators of inflammation[J]. American Journal of Physiology-Renal Physiology, 2004, 286(2): F189-F201.

      温馨提示:不可用于临床ZL。
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