GF 109203X hydrochloride (ab120844)

概述

  • 产品名称GF 109203X hydrochloride
  • 描述
    Potent, cell-permeable, ATP-competitive PKC inhibitor
  • 生物学描述Potent, cell-permeable, ATP-competitive PKC inhibitor (IC50 values for PKC subtypes are 50 (α), 17 (βI), 16 (βII) and 20 nM (γ)). Inhibits PKC over other kinases (IC50 values are 50 nM (MAPKAP), 100 nM (p70 S6 kinase), 2 μM (cAMP-dependent protein kinase) and 0.7 μM (phosphorylase kinase)). Crosses the blood-brain barrier.
  • 纯度> 99%

性能

  • 化学名称3-[1-(Dimethylaminopropyl)indol-3-yl]-4-(indol-3-yl)maleimide hydrochloride
  • 分子量448.95
  • 化学结构Chemical Structure
  • 分子式C25H24N4O2.HCl
  • CAS编号176504-36-2
  • PubChem识别号6419775
  • 存放说明Store at +4°C. Store under Desiccating conditions. The product can be stored for up to 12 months.
  • 溶解度概述Soluble in DMSO to 100 mM
  • 处理

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILESCN(C)CCCN1C=C(C2=CC=CC=C21)C3=C(C(=O)NC3=O)C4=CNC5=CC=CC=C54.Cl
  • 来源

    Synthetic

  • 研究领域

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    GF 109203X hydrochloride (ab120844)参考文献

    This product has been referenced in:
    • Cheung HH  et al. Inhibition of protein kinase C reduces ischemia-induced tyrosine phosphorylation of the N-methyl-d-aspartate receptor. J Neurochem 86:1441-9 (2003). Read more (PubMed: 12950452) »
    • Alessi DR The protein kinase C inhibitors Ro 318220 and GF 109203X are equally potent inhibitors of MAPKAP kinase-1beta (Rsk-2) and p70 S6 kinase. FEBS Lett 402:121-3 (1997). Read more (PubMed: 9037179) »
    • Toullec D  et al. The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C. J Biol Chem 266:15771-81 (1991). Read more (PubMed: 1874734) »

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