GF 109203X
Tocris Bioscience | Catalog # 0741
Key Product Details
Description
Alternative Names
Product Description
GF 109203X is a very potent and selective inhibitor of protein kinase C, selective for the α and β1 isoforms (IC50 values are 0.0084, 0.0180, 0.210, 0.132, and 5.8 μM for α, β1, δ, ε and ζ isoforms respectively). Selective over MLCK, PKG and PKA (IC50 values are 0.6, 4.6, and 33 μM respectively). Potent antagonist at the 5-HT3 receptor (Ki = 29.5 nM). Anti-inflammatory in vivo.
Product Specifications for GF 109203X
Molecular Weight
Formula
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Purity
Chemical Name
CAS Number
PubChem ID
InChI Key
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The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 10.31 | 25 |
Preparing Stock Solutions for GF 109203X
The following data is based on the product molecular weight 412.49.
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.25 mM | 9.70 mL | 48.49 mL | 96.97 mL |
| 1.25 mM | 1.94 mL | 9.70 mL | 19.39 mL |
| 2.5 mM | 0.97 mL | 4.85 mL | 9.70 mL |
| 12.5 mM | 0.19 mL | 0.97 mL | 1.94 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 317 publications citing the usage of this product.
- Jiang Heat shock protein 90-mediated inactivation of nuclear factor-κB switches autophagy to apoptosis through becn1 transcriptional inhibition in selenite-induced NB4 cells. Mol.Biol.Cell. 2011 PMID: 21346199
- Toullec The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C. J.Biol.Chem. 1991 PMID: 1874734
- Jacobson Anti-inflammatory properties of Go 6850: a selective inhibitor of protein kinase C. J.Pharmacol.Exp.Ther. 1995 PMID: 7473193
- Martiny-Baron Selective inhibition of protein kinase C isozymes by the indolocarbazole Go 6976. J.Biol.Chem. 1993 PMID: 8486620
- Coultrap Competitive antagonism of the mouse 5-hydroxytryptamine3 receptor by bisindolylmaleimide I, a "selective" protein kinase C inhibitor. J.Pharmacol.Exp.Ther. 1999 PMID: 10381762
Product Documents for GF 109203X
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for GF 109203X
For research use only
Related Research Areas
Citations for GF 109203X
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Species: RatAssay Type: In VitroCell Line/Tissue: HippocampusVerified Customer | Posted 07/21/2019GF 109203X (GF-109) was used to clarify an impact of PKC on average open time of GABA-A receptor channel. Experiment on outside-out membrane patches (OOP) and nucleated patches (NP) excised from hippocampal granule cells displayed a significant effect of GF-109 in NPs only. This confirms modulation of GABA-A receptor opening by PKA and ensures absence of GF-109 side effects on GABA-A receptors (since no effect was observed in OOPs).
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