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SID: 26759486

Inhibitor Libraries

Inhibitor Database

Inhibitor Resource
  SB 218078
Cat. No. 559402  
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Checkpoint Kinase

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

Yellow solid. PROTECT FROM LIGHT. PACKAGED UNDER INERT GAS. An indolocarbazole derivative that acts as a potent and selective inhibitor of checkpoint kinase (Chk1) in vitro. It inhibits Chk1 phosphorylation of cdc25C with an IC50 of 15 nM. However, SB-218078 is a much weaker inhibitor of Cdc2 (IC50 = 250 nM) and PKC (IC50 = 1 µM). Purity: ≥90% by HPLC. CAS 135897-06-2.

Ref.: Zhao, B., et al. 2002. J. Biol. Chem. 277, 46609. Jackson, J.R., et al. 2000. Cancer Res. 60, 566

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SolubilityMolecular FormulaMol. Wt.
DMSO C24H15N3O3 393.4 


Available Separately:
220479: Chk1, His•Tag®, Human, Recombinant, S. frugiperda
CBA020: K-LISA™ Checkpoint Activity Kit

Related Literature:

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Material Safety Data Sheets:
559402: SB 218078 - English
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Related Categories:
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Checkpoint Kinase