• 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

KRCA-0008

CAS No. 1472795-20-2

KRCA-0008 ( KRCA 0008;KRCA0008 )

产品货号. M12023 CAS No. 1472795-20-2

KRCA-0008 is a potent, selective ALK inhibitor with IC50 of 12 nM (wt ALK).

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥316 有现货
10MG ¥551 有现货
25MG ¥1045 有现货
50MG ¥2066 有现货
100MG ¥3491 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
    KRCA-0008
  • 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
    KRCA-0008 is a potent, selective ALK inhibitor with IC50 of 12 nM (wt ALK).
  • 产品描述
    KRCA-0008 is a potent, selective ALK inhibitor with IC50 of 12 nM (wt ALK), also is potent against various ALK mutants, including L1196M, F1174L, R1275Q, and C1156Y (IC50=5-75 nM); weakly inhibits IR (IC50=210 nM), inhibits H3122 and BaF3 EML4-ALK L1196M cell proliferation with IC50 of 80 and 68 nM, respectively; demonstrates in vivo efficacy comparable to Crizotinib in xenograft mice model, has drug-like properties without hERG concerns.
  • 同义词
    KRCA 0008;KRCA0008
  • 通路
    Angiogenesis
  • 靶点
    ALK
  • 受体
    ACK;ALK
  • 研究领域
    Cancer
  • 适应症
    ——

化学信息

  • CAS Number
    1472795-20-2
  • 分子量
    609.12
  • 分子式
    C30H37ClN8O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    10 mM in DMSO
  • SMILES
    ClC1=CN=C(NC2=CC=C(N3CCN(C(C)=O)CC3)C=C2OC)N=C1NC4=CC=C(N5CCN(C(C)=O)CC5)C=C4OC
  • 化学全称
    Ethanone, 1,1'-[(5-chloro-2,4-pyrimidinediyl)bis[imino(3-methoxy-4,1-phenylene)-4,1-piperazinediyl]]bis-

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. Park CH, et al. Bioorg Med Chem Lett. 2013 Nov 15;23(22):6192-6.
2. Kang CH, et al. Biochem Biophys Res Commun. 2015 Aug 28;464(3):762-7.
3. Lee HJ, et al. Arch Pharm Res. 2014;37(9):1130-8.
产品手册
关联产品
  • ASP3026

    ASP3026 is a potent small molecule ALK inhibitor with IC50 of 3.5, 10, 5.4 and 6.8 nM for wt ALK, ALK F1174L, ALK R1275Q and NPM1-ALK, respectively.

  • LDN193189 hydrochlor...

    LDN193189 is a potent, selective BMP type I receptor that inhibits BMP4-induced phosphorylation of SMAD1/5/8 with IC50 of 5 nM.

  • 5-phenylthieno[2,3-d...

    5-phenylthieno[2,3-d]pyrimidin-4-amine is a chemical compound.