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Minisite
血管生成
Fostamatinib (R788)
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
阿拉丁 | 生产商 | 上海 | 现货 |
产品参数
货号 | CAS号 | 操作 |
---|---|---|
F129915-10mg | 901119-35-5 | 询价 |
F129915-50mg | 901119-35-5 | 询价 |
F129915-5mg | 901119-35-5 | 询价 |
产品介绍
- 分子式 C23H26FN6O9P
- 分子量580.46
属性
溶解性 |
|
存贮条件 | 储存温度-20°C |
描述
应用 | An inhibitor to spleenic kinase-mediated IgG Fc receptor signaling |
产品介绍 | Fostamatinib (R788)是活性代谢产物R406的前体药物,是一种Syk抑制剂,IC50为41 nM,强效抑制Syk但不抑制Lyn,对Flt3作用效果低5倍。Phase 3。 |
备注 | Fostamatinib (R788), a prodrug of the active metabolite R406, is a Syk inhibitor with IC50 of 41 nM, strongly inhibits Syk but not Lyn, 5-fold less potent to Flt3. Phase 2. |
生化机理 | R788 (Fostamatinib) is an important spleen tyrosine kinase (Syk) inhibitor, showing efficacy against kinase-mediated IgG Fc gamma receptor signaling. R788 inhibits the activation of mast cells, macrophages, and B-cells and related inflammatory responses and tissue damage. In one study, inhibition of BCR signaling with R788 affected the growth of certain leukemia cell lines. These leukemia cells express stereotyped BCRs that react with auto-antigens exposed on the surface of senescent or apoptotic cells, suggesting that they are antigen driven. |
别名 | 6-[[5-氟-2-[(3,4,5-三甲氧基苯基)氨基]-4-嘧啶基]氨基]-2,2-二甲基-4-[(磷酰氧基)甲基]-2H-吡啶并[3,2-b]-1,4-恶嗪-3(4H)-酮;R788;(6-(5-fluoro-2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-ylamino)-2,2-dimethyl-3-oxo-2,3-dihydropyrido[3,2-b][1,4]oxazin-4-yl)methyl dihydrogen phosphate;R 788; R-788 |
Fostamatinib (R788)信息由上海阿拉丁生化科技股份有限公司为您提供,如您想了解更多关于Fostamatinib (R788)报价、型号、参数等信息,欢迎来电或留言咨询。
注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途