您的购物车当前为空
ZM323881是一种有效的选择性VEGFR2抑制剂,IC50值小于2 nM。

ZM323881是一种有效的选择性VEGFR2抑制剂,IC50值小于2 nM。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 25 mg | ¥ 10,600 | 1-2周 | |
| 50 mg | ¥ 13,800 | 1-2周 | |
| 100 mg | ¥ 17,500 | 1-2周 |
| 产品描述 | ZM323881 is a potent and selective inhibitor of VEGFR2 with an IC 50 of less than 2 nM. |
| 靶点活性 | VEGFR2:2 nM |
| 体外活性 | ZM323881 is an anilinoquinazoline that potently inhibits VEGFR2 (KDR) tyrosine kinase activity and demonstrates excellent selectivity compared with other receptor tyrosine kinases, including PDGFRβ, FGFR1, EGFR and erbB2 (IC 50 >50 μM). ZM323881 inhibits VEGF-A-induced endothelial cell proliferation(IC 50 =8 nM) and VEGFR2 tyrosine phosphorylation [1]. ZM323881 inhibits activation of VEGFR-2, but not of VEGFR-1, epidermal growth factor receptor (EGFR), platelet-derived growth factor receptor (PDGFR), or hepatocyte growth factor (HGF) receptor. In HAECs, ZM323881 completely inhibits VEGF-induced ERK phosphorylation at 1 μM [2]. |
| 分子量 | 375.4 |
| 分子式 | C22H18FN3O2 |
| CAS No. | 193001-14-8 |
| Smiles | N(C=1C2=C(C=C(OCC3=CC=CC=C3)C=C2)N=CN1)C4=C(F)C=C(C)C(O)=C4 |
| 密度 | 1.342 g/cm3 (Predicted) |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
对于不同动物的给药剂量换算,您也可以参考 更多