ULS 欢迎您!
ULS 欢迎您!
> 产品中心 > 抑制剂 & 激动剂 > TGF-beta/Smad > PKC

SB-218078

Cat. No.:YN310080

  • CAS No. :135897-06-2

    • 产品资料
    • 生物活性
    • 参考文献
    • 产品名称: SB-218078
      CAS No.: 135897-06-2
      Chemical Name: 9,10,11,12-tetrahydro-9,12-epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-1,3(2H)-dione
      Synonyms:SB 218078,SB-218078
      分子量:393.39
      分子式:C₂₄H₁₅N₃O₃
      SMILES:O=C1NC(C(C2=C3N(C4CCC5O4)C6=CC=CC=C62)=C1C7=C3N5C8=CC=CC=C78)=O
      存储:Please store the product under the recommended conditions in theCertificate of Analysis.
      运输:Room temperature in continental US; may vary elsewhere.
      Select Batch:
      Purity: 98%
    • 产品描述: SB-218078 是一种有效的,选择性,ATP 竞争性且细胞可渗透的检查点激酶 1 (Chk1) 抑制剂,可抑制 cdc25C 的Chk1磷酸化,IC50为 15 nM。SB-218078 对Cdc2(IC50为 250 nM) 和PKC(IC50为 1000 nM) 的抑制作用较弱。SB-218078 通过 DNA 损伤和细胞周期停滞诱导细胞凋亡。
      IC50和靶点: [{name:"Chk1:15 nM (IC50)"},{name: "Cdc2:250 nM (IC50)"},{name: "PKC:1000 nM (IC50)'}, 'Apoptosis']
      In Vitro:
      In Vivo:
      Clinical Trial:
      Solvent & Solubility:
    • Jackson, J.R., Gilmartin, A., Imburgia, G., et al.An indolocarbazole inhibitor of human checkpoint kinase (Chk1) abrogates cell cycle arrest caused by DNA damageCancer Res.60(3),566-572(2000)

      Tandon, M., Johnson, J., Li, Z., et al.New pyrazolopyrimidine inhibitors of protein kinase d as potent anticancer agents for prostate cancer cellsPLoS One8(9),e75601(2013)

      Kawabe, T.G2 checkpoint abrogators as anticancer drugsMol. Cancer Ther.3(4),513-519(2004)

    • 摩尔计算器
    • 稀释计算器
    摩尔浓度计算器方程 :
    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    计算

    质量 浓度 体积 分子量
    稀释计算器 :
    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
    • C1
      V1
      C2
      V2
    • 您最近查看的产品:
    相关产品


    ULS 的所有产品和服务仅用于科学研究,我们不为任何其他用途提供产品和服务(也不为任何个人提供产品和服务)Copyright © 2020-2021 ULS. All Rights Reserved. 备案号:粤ICP备2021013238号-1
    0.451601s