| CAS NO: | 912806-16-7 |
| 包装 | 价格(元) |
| 1mg | 电议 |
| 5mg | 电议 |
| 25mg | 电议 |
| Cas No. | 912806-16-7 |
| 化学名 | 4-((5-(cyclopropylcarbamoyl)-2-methylphenyl)amino)-5-methyl-N-propylpyrrolo[2,1-f][1,2,4]triazine-6-carboxamide hydrochloride |
| Canonical SMILES | O=C(C1=CN2N=CN=C(NC3=CC(C(NC4CC4)=O)=CC=C3C)C2=C1C)NCCC.Cl |
| 分子式 | C22H27ClN6O2 |
| 分子量 | 442.94 |
| 溶解度 | ≥ 44.3mg/mL in DMSO with gentle warming |
| 储存条件 | Store at -20°C |
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
| Shipping Condition | Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request |
| 产品描述 | BMS-582949 hydrochloride is a novel, potent and highly selective p38α mitogen-activated protein kinase (p38α MAPK) inhibitor [1]. The p38α MAP kinase plays a critical role in regulating the production of many inflammatory cytokines, including TNF-α and IL-1β. Excessive production of TNF-α and IL-1β has been implicated in many inflammatory diseases [1]. BMS-582949 hydrochloride potently inhibited the activity of p38α MAPK with the IC50 value of 13 nM [1]. BMS-582949 showed no significant effects on cytochrome P450 isozymes 1A2, 2C9, 2C19, and 2D6 with the IC50 values of >40 μM. BMS-582949 weakly inhibited the activity of CYP3A4, with the IC50 value of 18-40 μM. BMS-582949 displayed >2000-fold selectivity for p38α over a diverse panel of 57 kinases, include serine kinases, receptor tyrosine kinases, nonreceptor tyrosine kinases, and the p38γ and δ isoforms. BMS-582949 showed 450-fold selectivity over Jnk2, a MAP kinase involved in inflammation, and 190-fold selective over Raf [1]. In mice, after oral administration of BMS-582949 (10 mg/kg), the clearance rate for BMS-582949 is 4.4 mL/min/kg. BMS-582949 exhibited oral bioavailability values of 90% and 60% in mice and rats, respectively [1]. BMS-582949 is currently under Phase II clinical trials for the treatment of inflammatory diseases. In stable atherosclerosis, treatment with BMS-582949 for 12 weeks did not reduce arterial inflammation or hs-CRP compared to placebo whereas intensification of statin therapy significantly decreased arterial inflammation [2]. References: |
m.cnreagent.com