Overview
| MDL | MFCD30502665 |
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| Molecular Weight | 483.39 |
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| Molecular Formula | C22H18F5N3O4 |
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| SMILES | O=C(C1C=CC([C@H](C)NC(=O)C2C(C(F)F)=NN(C)C=2OC2C=C(C(F)(F)F)C=CC=2)=CC=1)O |
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For research use only.
Storage
3 years,-20°C,powder
1 years,-80°C,in solvent
Shipping
Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)
Preparing Stock Solutions
| 1 mg | 5 mg | 10 mg |
| 1 mM | 2.0687 mL | 10.3436 mL | 20.6872 mL |
| 5 mM | 0.4137 mL | 2.0687 mL | 4.1374 mL |
| 10 mM | 0.2069 mL | 1.0344 mL | 2.0687 mL |
| 50 mM | 0.0414 mL | 0.2069 mL | 0.4137 mL |
Description
E7046 (ER-886406, Palupiprant, AN0025) is a selective inhibitor of the with IC50 of 13.5 nM and Ki of 23.14 nM.
Targets
EP4 [1] (Cell-free assay) | EP4 [1] (Cell-free assay) |
| 13.5nM | 23.14 nM(Ki) |
In vitro
E7046 has specific and potent inhibitory activity on PGE-mediated pro-tumor myeloid cell differentiation and activation.