| CAS: | 956906-93-7 | ||
| 分子式: | C20H20N8O4S | ||
| 分子量: | 468.49 | ||
| 英文名称: |
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| 用途: | PF-04217903 methanesulfonate是ATP竞争性c-Met抑制剂,IC50为4.8 nM,对Y1230C突变型无活性。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||||||||||||
| P876145 | MACKLIN | PF-04217903 methanesulfonate | ≥99% | 254元/10mg; 760元/50mg; | 咨询 | ||||||||||||||||||||||||||||||||||||||||
储存:2-8℃ | |||||||||||||||||||||||||||||||||||||||||||||
| SML0263 | Sigma-Aldrich | PF-04217903 | ≥98% (HPLC) | 1480.38元/5 MG; 5967.79元/25 MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||||
产品说明 应用 PF-04217903 has been used as tyrosine-protein kinase Met (C-Met) selective inhibitor in Madin-Darby Canine kidney (MDCK) cells and NT2D1 non-seminoma cells. 包装 5, 25 mg in glass bottle 生化/生理作用 PF-04217903 is a highly selective, potent inhibitor of the hepatocyte growth factor receptor c-Met. PF-04217903 inhibits endogenous, wild type c-Met in A549 human lung carcinoma cells with an IC50 of 4.8 nM. The compund displays 1000-fold selectivity against a panel of 208 other kinases. 特点和优势 This compound is featured on the Met page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here. 基本信息
产品性质
安全信息
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