CAS NO: | 623152-17-0 |
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 |
Molecular Weight (MW) | 406.48 |
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Formula | C22H26N6O2 |
CAS No. | 912806-16-7 (HCl); 623152-17-0 (free base); |
Storage | -20℃ for 3 years in powder form |
-80℃ for 2 years in solvent | |
Solubility (In vitro) | DMSO: 81 mg/mL (199.3 mM) |
Water: <1 mg/mL | |
Ethanol: <1 mg/mL | |
SMILES | O=C(C1=CN2N=CN=C(NC3=CC(C(NC4CC4)=O)=CC=C3C)C2=C1C)NCCC |
Synonyms | PS540446; BMS-582949; BMS 582949; PS-540446; PS 540446; BMS582949; BMS582949 free base; Chemical Name: 4-((5-(cyclopropylcarbamoyl)-2-methylphenyl)amino)-5-methyl-N-propylpyrrolo[2,1-f][1,2,4]triazine-6-carboxamide Exact Mass: 406.2117 |
In Vitro | In vitro activity: BMS-582949 is found to inhibit p38 activation in cells, as measured by phosphorylation of p38. BMS-582949 treatment of cells in which p38 has been activated by LPS rapidly reversed p38 activation as shown by loss of phosphorylation of p38. BMS-582949 is therefore a dual action p38 kinase inhibitor, inhibiting both p38 kinase activity and p38 activation in cells. BMS-582949 binding to p38a results in a conformational change of the activation loop which is phosphorylated by upstream kinases, therefore it inhibits phosphorylation of p38 by upstream MKK by inducing a less accessible conformation of the activation loop. Kinase Assay: BMS-582949 was found to be 450-fold selective over Jnk2, a MAP kinase involved in inflammation, and 190-fold selective against Raf. Moreover, the binding mode of BMS-582949 with p38R was further demonstrated by X-ray crystallographic analyses. Cell Assay: BMS-582949 inhibits both p38 kinase activity and activation of p38. BMS-582949 is found to inhibit p38 activation in cells, as measured by phosphorylation of p38. BMS-582949 treatment of cells in which p38 has been activated by LPS rapidly reversed p38 activation as shown by loss of phosphorylation of p38. |
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In Vivo | The mouse clearance rate for BMS-582949 is 4.4 mL/min/kg. And at an oral dose of 10 mg/kg, the mouse AUC0-8 h for BMS-582949 is 75.5 μMoh. BMS-582949 exhibited oral bioavailability values of 90% and 60% in mice and rats, respectively. |
Animal model | Mouse |
Formulation & Dosage | Oral dose of 10 mg/kg |
References | J Med Chem. 2010 Sep 23;53(18):6629-39; Arthritis Rheum. 2010, 62 Suppl 10:1513. |