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Amfenac Sodium Monohydrate

CAS No. 61618-27-7

Amfenac Sodium Monohydrate ( Amfenac sodium H2O )

产品货号. M15326 CAS No. 61618-27-7

Amfenac Sodium Hydrate 是一个 COX-2 抑制剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
10MG ¥103 有现货
25MG ¥166 有现货
50MG ¥240 有现货
100MG ¥340 有现货
500MG ¥821 有现货
1G ¥1197 有现货
1 mL x 10 mM in DMSO ¥116 有现货

生物学信息

  • 产品名称
    Amfenac Sodium Monohydrate
  • 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
    Amfenac Sodium Hydrate 是一个 COX-2 抑制剂。
  • 产品描述
    Amfenac Sodium monohydrate is a non-steroidal analgesic anti-inflammatory drug with acetic acid moiety.(In Vitro):Cells transfected to express COX-2 have a higher proliferation rate than those do not. The addition of Amfenac Sodium Hydrate significantly decreases the proliferation rate of all cell lines. Nitric oxide production by macrophages is inhibited by the addition of melanoma conditioned medium, the addition of Amfenac Sodium Hydrate partially overcomes this inhibition. Results show that Amfenac Sodium Hydrate inhibits the release of B-glucuronidase: 5×10-4 M Amfenac Sodium Hydrate inhibits the release of the enzyme 35.3 and 16.3% in the presence of 10-8, and 10-7 M FMLP, respectively. Addition of 10-4 M Amfenac Sodium Hydrate causes 28.3% inhibition of aggregation of polgmorphonuclear leukocgtes (PMNs) during incubation for 16 min with 10-8 M FMLP.
  • 体外实验
    Cells transfected to express COX-2 have a higher proliferation rate than those do not. The addition of Amfenac Sodium Hydrate significantly decreases the proliferation rate of all cell lines. Nitric oxide production by macrophages is inhibited by the addition of melanoma conditioned medium, the addition of Amfenac Sodium Hydrate partially overcomes this inhibition. Results show that Amfenac Sodium Hydrate inhibits the release of B-glucuronidase: 5×10-4 M Amfenac Sodium Hydrate inhibits the release of the enzyme 35.3 and 16.3% in the presence of 10-8, and 10-7 M FMLP, respectively. Addition of 10-4 M Amfenac Sodium Hydrate causes 28.3% inhibition of aggregation of polgmorphonuclear leukocgtes (PMNs) during incubation for 16 min with 10-8 M FMLP.
  • 体内实验
    ——
  • 同义词
    Amfenac sodium H2O
  • 通路
    Chromatin/Epigenetic
  • 靶点
    COX
  • 受体
    COX-1| COX-2
  • 研究领域
    Other Indications
  • 适应症
    ——

化学信息

  • CAS Number
    61618-27-7
  • 分子量
    295.27
  • 分子式
    C15H12NO3·H2O·Na
  • 纯度
    >98% (HPLC)
  • 溶解度
    Ethanol: 4 mg/mL (13.54 mM); Water: 59 mg/mL (199.81 mM); DMSO: 59 mg/mL (199.81 mM)
  • SMILES
    O=C([O-])CC1=CC=CC(C(C2=CC=CC=C2)=O)=C1N.[H]O[H].[Na+]
  • 化学全称
    Benzeneacetic acid, 2-amino-3-benzoyl-, sodium salt, monohydrate

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. Gamache DA, et al. Inflammation, 2000, 24(4), 357-370.
产品手册
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