| 货号:22205-1 mg | 规格:1 mg | 目录价:¥563 |
| 货号:22205-10 mg | 规格:10 mg | 目录价:¥3511 |
| 货号:22205-25 mg | 规格:25 mg | 目录价:¥8067 |
| 货号:22205-5 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:
FRAX597
产品描述:
A PAK inhibitor selective for group I PAKs (IC50s = 7.7, 12.8, and 19.3 nM for PAK 1, 2, and 3, respectively) over group II PAKs (IC50 > 10 µM for PAK4 and 50 = 70 nM); reduces proliferation and survival of transformed Schwann cells, ovarian, and pancreatic cells; works synergistically with gemcitabine in pancreatic cancer models in vitro and in vivo
保存温度:
-20
运输温度:
-20
预期分子量:
558.1
产品形式:
A crystalline solid
纯度:
≥98%
CAS号:
1286739-19-2
分子式:
C29H28ClN7OS
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