CAS NO: | 836620-48-5 |
规格: | ≥98% |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
250mg | 电议 |
500mg | 电议 |
1g | 电议 |
Molecular Weight (MW) | 347.39 |
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Formula | C18H22FN3O3 |
CAS No. | 836620-48-5 |
Storage | -20℃ for 3 years in powder form |
-80℃ for 2 years in solvent | |
Solubility (In vitro) | DMSO: ≥ 5 mg/mL |
Water: N/A | |
Ethanol: N/A | |
Chemical Name | 5-amino-7-(cyclohexylamino)-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid |
Synonyms | AS1842856; AS-1842856; AS 1842856 |
In Vitro | In vitro activity: AS1842856 potently inhibits human Foxo1 transactivation and reduces glucose production through the inhibition of glucose-6 phosphatase and phosphoenolpyruvate carboxykinase mRNA levels in a rat hepatic cell line Kinase Assay: AS1842856 is a potent and cell-permeable Foxo1 inhibitor with an IC50 of 30 nM. Cell Assay: Rat hepatoma Fao cells are cultured in DMEM with 5.5 mM glucose and 10% FBS. Glucose production rate is measured using glucose CII-test reagent. In brief, after 18 h of treatment with either insulin or AS1842856 at the indicated concentrations, the cells are ished three times with PBS. The cells are then incubated for 3 h at 37°C in 5% CO2 in a glucose production buffer (glucose-free DMEM, pH 7.4, containing 20 mM sodium pyruvate, without phenol red). |
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In Vivo | Oral administration of AS1842856 to diabetic db/db mice leads to a drastic decrease in fasting plasma glucose level via the inhibition of hepatic gluconeogenic genes, whereas administration to normal mice has no effect on the fasting plasma glucose level. Treatment with AS1842856 also suppresses an increase in plasma glucose level caused by pyruvate injection in both normal and db/db mice. |
Animal model | Diabetic db/db mice |
Formulation & Dosage | AS1842856 is dissolved in 6% cyclodextrin for oral administration. |
References | Mol Pharmacol. 2010 Nov;78(5):961-70. |