• 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

DEL-22379

CAS No. 181223-80-3

DEL-22379 ( DEL22379 | DEL 22379 )

产品货号. M12782 CAS No. 181223-80-3

一种 ERK 二聚化小分子抑制剂,IC50 为 0.5 uM,不影响 ERK 磷酸化。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥348 有现货
5MG ¥551 有现货
10MG ¥1021 有现货
25MG ¥1863 有现货
50MG ¥2989 有现货
100MG ¥4447 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
    DEL-22379
  • 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
    一种 ERK 二聚化小分子抑制剂,IC50 为 0.5 uM,不影响 ERK 磷酸化。
  • 产品描述
    A small molecule inhibitor of ERK dimerization with IC50 of 0.5 uM, without affecting ERK phosphorylation; prevents tumorigenesis by RAS-ERK pathway oncogenes.
  • 体外实验
    DEL-22379 is an ERK dimerization inhibitor. DEL-22379 abolishes EGF-induced co-immunoprecipitation of ectopic ERK2 molecules tagged with hemagglutinin (HA) or FLAG epitopes, with an estimated half-maximal inhibitory concentration (IC50) of ~0.5 μM. DEL-22379 inhibits growth of tumor cells harboring RAS-ERK pathway oncogenes. The biological effects of DEL-22379 are investigated on tumor cells in culture. The cytostatic effects of DEL-22379 are compared to those of the MEK inhibitor PD-0325901 and the ERK kinase inhibitor SCH-772984, as reflected by their half-maximal growth inhibitory concentrations (GI50). Cell lines harboring mutant BRAF are the most sensitive to the three compounds. In comparison, wild-type (WT) cell lines for BRAF and RAS are the most resistant, and RAS mutant cells exhibit a range of sensitivities. In cells showing different oncogenic genotypes, distinct sensitivity to DEL-22379 can not be attributed to variations on its effects on dimerization, because DEL-22379 displays similar dimerization- and cytoplasmic signaling-inhibitory dose responses (IC50 of 150-400 nM) regardless of the genotype.
  • 体内实验
    To test DEL-22379 antitumor effects, some of the aforementioned cell lines are xenografted into nude mice, and tumor growth is monitored after intra-peritoneal administration of DEL-22379 at 15 mg/kg. At such a dose, inhibition of ERK dimerization is evident in liver extracts and in xenografted tumors. DEL-22379 markedly inhibits tumor progression for A375 cells (BRAF mutant).
  • 同义词
    DEL22379 | DEL 22379
  • 通路
    MAPK/ERK Signaling
  • 靶点
    ERK
  • 受体
    ERK
  • 研究领域
    Cancer
  • 适应症
    ——

化学信息

  • CAS Number
    181223-80-3
  • 分子量
    444.5255
  • 分子式
    C26H28N4O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: ≥ 30 mg/mL
  • SMILES
    O=C(NC1=CC2=C(NC(/C2=C/C3=CNC4=C3C=C(OC)C=C4)=O)C=C1)CCN5CCCCC5
  • 化学全称
    1-Piperidinepropanamide, N-[2,3-dihydro-3-[(5-methoxy-1H-indol-3-yl)methylene]-2-oxo-1H-indol-5-yl]-

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. Herrero A, et al. Cancer Cell. 2015 Aug 10;28(2):170-82.
产品手册
关联产品
  • AX-15836

    一种有效的、高选择性的 ERK5 抑制剂,IC50 为 8 nM;对 BRD4 的亲和力很小(Kd=3.6 uM)。

  • ERK-IN-4

    ERK-IN-4 是一种 ERK 抑制剂,优先结合 ERK2,Kd 为 5 μM。ERK-IN-4 特异性抑制 ERK Rsk-1 和 Elk-1 磷酸化。ERK-IN-4 对其上游激活剂 MEK1/2 的 ERK 蛋白磷酸化几乎没有影响。

  • 1-Butanol

    1-丁醇具有抗氧化作用,可降低高血糖。 1-丁醇通过抑制肥大细胞脱颗粒和炎症细胞因子的表达而具有抗过敏炎症作用。