Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Selective FTO inhibitor (IC50 = 0.81 μM). Exhibits <30-fold selectivity for FTO over ALKBH2, 3 and 5 and <100-fold selectivity over PHD2 and JMJD2A. Increases levels of modified N6-methyladenosine (m6A) in HeLa cells in a concentration-dependent manner.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
10 mg | 35 days | $ 545.00 |
Description | Selective FTO inhibitor (IC50 = 0.81 μM). Exhibits >30-fold selectivity for FTO over ALKBH2, 3 and 5 and >100-fold selectivity over PHD2 and JMJD2A. Increases levels of modified N6-methyladenosine (m6A) in HeLa cells in a concentration-dependent manner. |
Molecular Weight | 353.37 |
Formula | C19H19N3O4 |
CAS No. | 1808089-27-1 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Ethanol: 7.07 mg/mL(20 mM)
DMSO: 35.34 mg/mL(100 mM)
You can also refer to dose conversion for different animals. More
bottom
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
Ethyl LipotF 1808089-27-1 inhibitor inhibit