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Diciofenac

CAS No. 15307-86-5

Diciofenac ( —— )

产品货号. M12147 CAS No. 15307-86-5

双氯芬酸是一种非甾体类抗炎药 (NSAID),用于减轻炎症并在某些情况下作为镇痛药减轻疼痛。它以多种商品名作为药物提供或包含在药物中。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
500MG ¥340 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Diciofenac
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    双氯芬酸是一种非甾体类抗炎药 (NSAID),用于减轻炎症并在某些情况下作为镇痛药减轻疼痛。它以多种商品名作为药物提供或包含在药物中。
  • 产品描述
    Diclofenac is a nonsteroidal anti-inflammatory drug (NSAID) taken or applied to reduce inflammation and as an analgesic reducing pain in certain conditions. It is supplied as or contained in medications under a variety of trade names.(In Vitro):Diclofenac effectively blocks COX-1 mediated prostanoid production from U937 cell microsomes, with an IC50 of 7±3 nM.Diclofenac (1-60 μM; 1 day) induces neural stem cells (NSCs)death in a concentration-dependent manner.Diclofenac (10-60 μM; 6 hours) increases the expression of cleaved (activated) caspase-3.(In Vivo):Diclofenac (3 mg/kg, b.i.d., for 5 days) significantly increases faecal 51Cr excretion in rats, and such effect is also observed in squirrel monkeys after administrated of 1 mg/kg twice daily for 4 days.Diclofenac (10 mg/kg; administered via oral route just prior to induction of inflammation) shows in vivo anti-inflammatory activity in Wistar rats.
  • 体外实验
    Cell Viability Assay Cell Line:Neural stem cells (NSCs)Concentration:1, 3, 10, 30, 60 μM Incubation Time:1 day Result:Induction of cell death was concentration-dependent and the effect was not saturated at a concentration of up to 60 μM.Western Blot Analysis Cell Line:Neural stem cells (NSCs)Concentration:10, 30 or 60 μM Incubation Time:6 hours Result:The activation of caspase-3 was increased in a concentration-dependent manner.
  • 体内实验
    Animal Model:Male Sprague-Dawley rats (150±200 g)Dosage:3 mg/kg Administration:Oral administration, b.i.d., for 5 days Result:Resulted in a significant increase in faecal 51Cr excretion.Animal Model:Wistar rats (150-175 g) bearing Formalin-induced rat foot paw edema model Dosage:10 mg/kg Administration:Administered via oral route just prior to induction of inflammation Result:Showed in vivo anti-inflammatory activity (% edema inhibition=29.2, 1 h; 22.2, 3 h; 20, 6 h).
  • 同义词
    ——
  • 通路
    Chromatin/Epigenetic
  • 靶点
    COX
  • 受体
    COX
  • 研究领域
    Inflammation/Immunology
  • 适应症
    ——

化学信息

  • CAS Number
    15307-86-5
  • 分子量
    296.15
  • 分子式
    C14H11Cl2NO2
  • 纯度
    >98% (HPLC)
  • 溶解度
    Water: 2.37 mg/L
  • SMILES
    C1=CC=C(C(=C1)CC(=O)O)NC2=C(C=CC=C2Cl)Cl
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Prokkola JM, et al. Aquat Toxicol. 2015 Jan;158:116-24.
产品手册
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