• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Aceclofenac

CAS No. 89796-99-6

Aceclofenac ( Aceclofenac | YT-919 | YT 919 | YT919 | Airtal | Beofenac )

产品货号. M16460 CAS No. 89796-99-6

醋氯芬酸是双氯芬酸的非甾体抗炎药 (NSAID) 类似物。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
200MG ¥115 有现货
500MG ¥180 有现货
1G ¥226 有现货
1 mL x 10 mM in DMSO ¥238 有现货

生物学信息

  • 产品名称
    Aceclofenac
  • 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
    醋氯芬酸是双氯芬酸的非甾体抗炎药 (NSAID) 类似物。
  • 产品描述
    Aceclofenac is a non-steroidal anti-inflammatory drug (NSAID) analog of Diclofenac. It is used for the relief of pain and inflammation in rheumatoid arthritis, osteoarthritis and ankylosing spondylitis. (In Vitro):Aceclofenac (1-30 μM; 72 hours) significantly decreases interleukin-6 production and fully blocks prostaglandin E2 synthesis by IL-1β- or LPS-stimulated human chondrocytes.Aceclofenac inhibits COX-1 with IC50 values superior to 100 μM, but decreases by 50% COX-2 activity at the concentration of 0.77 μM in the whole blood test.Aceclofenac increases the synthesis of interleukin 1 receptor antagonist and decreases the production of nitric oxide in human articular chondrocytes.(In Vivo):Aceclofenac exhibits Cmax (4.59 μg/mL) following oral administration (rat 20 mg/kg).Aceclofenac exhibits terminal elimination half-life (rat 3.24 h) due to high plasma clearance (rat 1.10 L/h/kg) following intravenous injection (rat 10 mg/kg).
  • 体外实验
    Aceclofenac (1-30 μM; 72 hours) significantly decreases interleukin-6 production and fully blocks prostaglandin E2 synthesis by IL-1β- or LPS-stimulated human chondrocytes.Aceclofenac inhibits COX-1 with IC50 values superior to 100 μM, but decreases by 50% COX-2 activity at the concentration of 0.77 μM in the whole blood test.Aceclofenac increases the synthesis of interleukin 1 receptor antagonist and decreases the production of nitric oxide in human articular chondrocytes.
  • 体内实验
    Aceclofenac exhibits Cmax (4.59 μg/mL) following oral administration (rat 20 mg/kg).Aceclofenac exhibits terminal elimination half-life (rat 3.24 h) due to high plasma clearance (rat 1.10 L/h/kg) following intravenous injection (rat 10 mg/kg). Animal Model:Male Sprague-Dawley rats weighing 32-340 g Dosage:10 mg/kg for i.v., 20 mg/kg for p.o. (Pharmacokinetic Analysis) Administration:Oral administration and intravenous injection Result:T1/2 (3.24 h), Cmax (4.59 μg/mL for p.o.).
  • 同义词
    Aceclofenac | YT-919 | YT 919 | YT919 | Airtal | Beofenac
  • 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
    89796-99-6
  • 分子量
    354.18
  • 分子式
    C16H13Cl2NO4
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: 10 mM
  • SMILES
    O=C(OCC(O)=O)CC1=CC=CC=C1NC2=C(Cl)C=CC=C2Cl
  • 化学全称
    2-(2-(2-((2,6-dichlorophenyl)amino)phenyl)acetoxy)acetic acid

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.Ganesh M, et al. Int J Biol Macromol. 2015 Mar;74:310-7.
产品手册
关联产品
  • FK 3311

    FK 3311 是一种细胞渗透性口服磺酰苯胺,可作为 COX-2 抑制剂和非甾体抗炎药 (NSAID)。

  • Zaltoprofen

    Zaltoprofen 是一种 Cox-1 和 Cox-2 抑制剂,用于治疗关节炎。

  • Suxibuzone

    Suxibuzone 是一种用于治疗关节和肌肉疼痛的化合物。它是非甾体类抗炎药保泰松的前药。