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AZD2906, a selective glucocorticoid receptor (GR) agonist, demonstrates inhibitory concentrations (IC50s) of 2.2 nM in human GR, 0.3 nM in rat peripheral blood mononuclear cells (PBMC), 41.6 nM in human whole blood, and 7.5 nM in rat whole blood, respectively[1]. Additionally, it induces an increase in micronucleated immature erythrocytes within rat bone marrow.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
5 mg | $427 | 6-8 weeks | |
25 mg | $1,400 | 6-8 weeks | |
50 mg | $1,820 | 6-8 weeks | |
100 mg | $2,500 | 6-8 weeks |
Description | AZD2906, a selective glucocorticoid receptor (GR) agonist, demonstrates inhibitory concentrations (IC50s) of 2.2 nM in human GR, 0.3 nM in rat peripheral blood mononuclear cells (PBMC), 41.6 nM in human whole blood, and 7.5 nM in rat whole blood, respectively[1]. Additionally, it induces an increase in micronucleated immature erythrocytes within rat bone marrow. |
Targets&IC50 | GR (rat PBMC):0.3 nM, GR (human whole blood):41.6 nM, GR (human PBMC):2.2 nM, GR (rat whole blood):7.5 nM |
In vitro | AZD2906 is a selective glucocorticoid receptor (GR) with IC50 values of 2.2 nM and 0.3 nM in human and rat PBMC, and 41.6 nM and 7.5 nM in human and rat whole blood, respectively[1]. |
In vivo | AZD2906 (5, 25, 50 mg/kg, p.o.) increases micronucleated immature erythrocytes (MIE) in the bone marrow of rats after 2 days of treatment and induces glycogen accumulation in the liver at 5 and 25 mg/kg, p.o., while causing moderate to marked cortical lymphocytic atrophy in the thymus of rats[1]. |
Molecular Weight | 460.5 |
Formula | C26H25FN4O3 |
Cas No. | 1034148-15-6 |
Relative Density. | 1.33 g/cm3 (Predicted) |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
Solubility Information | DMSO: 125 mg/mL (271.44 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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