PD184352 (CI-1040)
Catalog No. A10212
PD184352 (CI-1040)是一种ATP非竞争性MEK1/2抑制剂,在基于细胞的测定中,IC50为17 nM,对MEK1/2的选择性是对MEK5的100倍。
- Sachio Suzuki, .et al. A chemogenetic platform for controlling plasma membrane signaling and synthetic signal oscillation, Cell Chem Biol, 2022, Sep 15;29(9):1446-1464 PMID: 35835118
- Masaru Yoshikawa, .et al. Synthetic Protein Condensates That Inducibly Recruit and Release Protein Activity in Living Cells, J Am Chem Soc, 2021, May 5;143(17):6434-6446 PMID: 33890764
Catalog Num | A10212 |
---|---|
M. Wt | 478.7 |
Formula | C17H14ClF2IN2O2 |
Purity | >98% |
Storage | at -20°C 3 years Powder |
CAS No. | 212631-79-3 |
Synonyms | CI-1040 |
SMILES | C1CC1CONC(=O)C2=C(C(=C(C=C2)F)F)NC3=C(C=C(C=C3)I)Cl |
PD184352 (CI-1040)是一种ATP非竞争性MEK1/2抑制剂,在基于细胞的测定中,IC50为17 nM,对MEK1/2的选择性是对MEK5的100倍。
Targets
MEK1 (Cell-free assay) | MEK2 (Cell-free assay) | |||
17 nM | 17 nM |
In vitro (25°C) | DMSO | 92 mg/mL (192.19 mM) | |
Water | Insoluble | ||
Ethanol | 13 mg/mL (27.15 mM) | ||
In vivo | 30% PEG400+0.5% Tween80+5% propylene glycol, pH 9 | 9 mg/mL | |
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 20.89 mL | 104.45 mL | 208.9 mL |
0.5 mM | 4.18 mL | 20.89 mL | 41.78 mL |
1 mM | 2.09 mL | 10.44 mL | 20.89 mL |
5 mM | 0.42 mL | 2.09 mL | 4.18 mL |
*The above data is based on the productmolecular weight 478.7 . 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.