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Etalocib

CAS No. 161172-51-6

Etalocib ( LY293111 | VML295 )

产品货号. M23713 CAS No. 161172-51-6

Etalocib 是一种新型二芳基醚羧酸衍生物,通过拮抗白三烯 B4 (LTB4) 受体或直接通过 5'-脂氧合酶,成为脂氧合酶途径的选择性且有效的抑制剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥2811 有现货
10MG ¥4560 有现货
25MG ¥7209 有现货
50MG ¥9963 有现货
100MG ¥13527 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Etalocib
  • 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
    Etalocib 是一种新型二芳基醚羧酸衍生物,通过拮抗白三烯 B4 (LTB4) 受体或直接通过 5'-脂氧合酶,成为脂氧合酶途径的选择性且有效的抑制剂。
  • 产品描述
    Etalocib is a novel diaryl ether carboxylic acid derivative, is a selective and potent inhibitor of the lipoxygenase pathway either via antagonism of the leukotriene B4 (LTB4) receptor or directly through 5'-lipoxygenase. It has antineoplastic activities.(In Vitro):Etalocib (LY293111) elicits a concentration-dependent inhibition of LTB4 induced CD11b up-regulation.Etalocib (LY293111) is an extremely potent and selective antagonist of human neutrophil function in vitro.Etalocib (LY293111, 250 and 500 nM, 24-72 h) induces apoptosis and inhibits proliferation in human pancreatic cancer cells.(In Vivo):Etalocib (LY293111) produces a dose-related inhibition of acute leukotriene B4-induced airway obstruction when administered i.v. (ED50=14 μg/kg) or p.o. (ED50=0.4 mg/kg).Etalocib (LY293111, 10 mg/kg) inhibits A23187-induced lung inflammatory changes at 1 h.Etalocib (LY293111, 250 mg/kg/day, orally) inhibits growth of human pancreatic cancer xenografts in athymic mice.
  • 体外实验
    Etalocib (LY293111) elicits a concentration-dependent inhibition of LTB4 induced CD11b up-regulation.Etalocib (LY293111) is an extremely potent and selective antagonist of human neutrophil function in vitro.Etalocib (LY293111, 250 and 500 nM, 24-72 h) induces apoptosis and inhibits proliferation in human pancreatic cancer cells. Cell Proliferation Assay Cell Line:MiaPaCa-2 and AsPC-1 human pancreatic cancer cells. Concentration:500 nM.Incubation Time:24, 48, and 72 h.Result:Caused both a concentration-dependent and time-dependent inhibition of thymidine incorporation in both MiaPaCa-2 and AsPC-1 human pancreatic cancer cells.Apoptosis Analysis Cell Line:MiaPaCa-2 and AsPC-1 human pancreatic cancer cells.Concentration:250 and 500 nM.Incubation Time:24 h.Result:Induced apoptosis in human pancreatic cancer cells.
  • 体内实验
    Etalocib (LY293111) produces a dose-related inhibition of acute leukotriene B4-induced airway obstruction when administered i.v. (ED50=14 μg/kg) or p.o. (ED50=0.4 mg/kg).Etalocib (LY293111, 10 mg/kg) inhibits A23187-induced lung inflammatory changes at 1 h.Etalocib (LY293111, 250 mg/kg/day, orally) inhibits growth of human pancreatic cancer xenografts in athymic mice. Animal Model:Guinea pigs.Dosage:1-10 mg/kg.Administration:Orally once.Result:A single 1 mg/kg oral dose inhibited excised lung gas volume increases by 76.7±7.1% (n=4, P<0.002) when given 8 h prior to leukotriene B4 challenge, and 28.6±20.3% (n=4, NS) when given 24 h before challenge.Had no effect (10 mg/kg) on pulmonary gas trapping at 1 h or 2 h after A23187 challenge. However, at 4 h, the pulmonary gas trapping response was significantly less than that of vehicle-treated controls and not different from sham values. The 10 mg/kg dose inhibited A23187-induced lung inflammatory changes at 1 h, but was without effect at 2 h or 4 h after challenge.
  • 同义词
    LY293111 | VML295
  • 通路
    Apoptosis
  • 靶点
    Apoptosis
  • 受体
    Apoptosis|LTB4
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    161172-51-6
  • 分子量
    544.6
  • 分子式
    C33H33FO6
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:100 mg/mL (183.62 mM; Need ultrasonic)
  • SMILES
    O=C(O)C1=CC=CC=C1OC2=CC=CC(OCCCOC3=C(CC)C=C(C4=CC=C(F)C=C4)C(O)=C3)=C2CCC
  • 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.P Marder, et al. Blockade of Human Neutrophil Activation by 2-[2-propyl-3-[3-[2-ethyl-4-(4-fluorophenyl)-5- Hydroxyphenoxy]propoxy]phenoxy]benzoic Acid (LY293111), a Novel Leukotriene B4 Receptor Antagonist. Biochem Pharmacol. 1995 May 26;49(11):1683-90.
产品手册
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