| 溶解性 | DMSO 85 mg/mL Water 10 mg/mL Ethanol 6 mg/mL |
| 存贮条件 | 储存温度-20°C |
| 备注 | Vatalanib (PTK787) is an inhibitor of VEGFR2/KDR with IC50 of 37 nM, less potent against VEGFR1/Flt-1, 18-fold against VEGFR3/Flt-4. Phase 1/2. |
| 生化机理 | Vatalanib (PTK787) is a novel VEGFR and c-Kit tyrosine kinases and angiogenesis inhibitor with IC50 of 0.037, 0.077, 0.27 and 0.73 μM for KDR, Flt-1, Flk and c-Kit, respectively. |
| 别名 | N-(4-chlorophenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine dihydrochloride;N-(4-chlorophenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine dihydrochloride |
瓦他拉尼 (PTK787)二盐酸盐
Vatalanib (PTK787) 2HCl （订货以英文为准）
编号：V125857
CAS号：212141-51-0
分子式：C20H17CL3N4
分子量：419.73
| 产品名称 | Vatalanib (PTK787) 2HCl |
| 中文名称 | 瓦他拉尼 (PTK787)二盐酸盐 |
| CAS号 | 212141-51-0 |
| 分子式（M.F.） | C20H17CL3N4 |
| 分子量（M.W.） | 419.73 |
| 储存条件 | -20°C储存 |
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