| Description | F1063-0967 is a Dual-specificity phosphatase 26 (DUSP26) inhibitor with an IC50 of 11.62 μM. |
| In vitro | 在浓度超过0.1μM时，F1063-0967显著诱导IMR32细胞发生凋亡。F1063-0967对IMR-32细胞线的凋亡诱导作用，其半抑制浓度（IC50）值为4.13μM。F1063-0967对HL7702细胞线无影响，并且对SH-SY5Y细胞线的抑制作用较小。 |
| Cell experiments | The IMR-32 cells are plated in 96-well plates with 1×103 cells per well. After the cells are allowed to settle for 24 h, F1063-0967 (0, 10, 1, and 0.1 μM) is added. An MTTassay is performed. For cell lines HL7702 and SH-SY5Y, the cells are allowed to settle for 24 h, F1063-0967 (10 μM) is added, then MTT assays are carried out after 72 h. |
| Target activity | DUSP26:11.62 μM |
| molecular weight | 484.59 |
| Molecular formula | C24H24N2O5S2 |
| CAS | 613225-56-2 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year |
| Solubility | DMSO: 60 mg/mL (123.82 mM) |
| References | 1. Ren JX, et al. Identification of novel dual-specificity phosphatase 26 inhibitors by a hybrid virtual screening approach based on pharmacophore and molecular docking. Biomed Pharmacother. 2017 May;89:376-385. |