United States (Change Country)R406 Chemical Structure
R406 is an orally available spleen tyrosine kinase inhibitor with an IC50 of 41 nM. R406 blocked Syk-dependent FcR-mediated activation of monocytes/macrophages and neutrophils and BCR-mediated activation of B lymphocytes. R406 has shown efficacy in a number of animal models of immune disorders. R406 inhibited airway hyperresponsiveness (AHR) and airway inflammation in mice, at least in part through alteration of mast cell and dendritic cell functions. Similarly, R406 treatment ameliorated joint inflammation in a number of rodent models of rheumatoid arthritis and also blocked JNK-mediated gene expression in human synoviocytes, suggesting a possible role in the treatment of rheumatoid arthritis. [1][2]
[1] Toxicology and Applied Pharmacology 2007;221:268–277
[2] Xenobiotica. 2010 Jun;40(6):415-23.
| Molecular Weight (WM): | 628.63 |
|---|---|
| Formula: | C22H23FN6O5.C6H6O3S |
| Solubility(R.T.:25°C): | DMSO 126mg/mL |
| Water <1mg/mL | |
| Ethanol 8mg/mL |
A collection of 715 inhibitors
A collection of 271 kinase inhibitors
A collection of 785 FDA approved drugs
A collection of 144 natural products
A collection of 84 chemotherapeutic agents
A collection of 1463 bioactive compounds
A collection of 117 tyrosine kinase inhibitors
;Clin Cancer Res, 2013, 19(3), 586-597 R406 purchased from Selleck
Keywords:buy R406 | R406 supplier | purchase R406 | R406 cost | R406 manufacturer | order R406 | R406 distributor