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折扣/货期| 货号：21386-1 mg | 规格：1 mg | 目录价：￥563 |
| 货号：21386-10 mg | 规格：10 mg | 目录价：￥4315 |
| 货号：21386-25 mg | 规格：25 mg | 目录价：￥8750 |
| 货号：21386-5 mg | 规格：5 mg | 目录价：￥2452 |
产品详情
* 以下信息仅供参考，详情请以原厂网站为准
产品名称:
BFH772
产品描述:
An inhibitor of VEGFR2 (IC50 = 0.0027 μM for the human receptor); selective for human VEGFR2 over mouse VEGFR2 and human VEGFR1 and VEGFR3 (IC50s = 1.5, 1.7, and 1.1 μM, respectively), as well as 40-fold selective over B-RAF, RET, and Tie2; inhibits VEGF-induced proliferation of HUVECs (IC50 = <0.01 nM); inhibits VEGF-induced increases in tissue weight and Tie2 levels in an angiogenesis chamber implant model in mice at 1 and 3 mg/kg per day; inhibits primary tumor and metastasis growth in a B16 melanoma mouse model at 3 mg/kg per day
保存温度:
-20
运输温度:
-20
预期分子量:
439.4
产品形式:
A crystalline solid
纯度:
≥95%
CAS号:
890128-81-1
分子式:
C23H16F3N3O3
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