Chemical Name: 5,7-Dibromo-6-fluoro-3,4-dihydro-2-methyl-1(2H)-quinolinecarboxaldehyde
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Uncompetitive Epac1 inhibitor. Blocks Epac-induced Rap activation and prevents isoprenaline-induced autophagy flux in cardiomyocytes. Has no effect on PKA activity in the presence of cAMP.
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Technical Data
M. Wt
351.01
Formula
C11H10Br2FNO
Storage
Store at -20°C
Purity
≥98% (HPLC)
CAS Number
143703-25-7
PubChem ID
21781066
InChI Key
ZZLQPWXVZCPUGC-UHFFFAOYSA-N
Smiles
BrC1=C(F)C(Br)=C(CCC(C)N2C=O)C2=C1
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
DMSO
35.1
100
ethanol
17.55
50
Preparing Stock Solutions
The following data is based on the product molecular weight 351.01. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
2.85 mL
14.24 mL
28.49 mL
5 mM
0.57 mL
2.85 mL
5.7 mL
10 mM
0.28 mL
1.42 mL
2.85 mL
50 mM
0.06 mL
0.28 mL
0.57 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Laurentet al (2015) Exchange protein directly activated by cAMP 1 promotes autophagy during cardiomyocyte hypertrophy. Cardiovasc.Res. 105 55 PMID: 25411381
Courilleauet al (2012) Identification of a tetrahydroquinoline analog as a pharmacological inhibitor of the cAMP-binding protein Epac. J.Biol.Chem. 287 44192 PMID: 23139415