| 货号:14932-10 mg | 规格:10 mg | 目录价:¥2251 |
| 货号:14932-25 mg | 规格:25 mg | 目录价:¥4677 |
| 货号:14932-5 mg | 规格:5 mg | 目录价:¥1206 |
| 货号:14932-50 mg | 规格:50 mg | 目录价:¥8750 |
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:
BX-795
产品描述:
A multi-kinase inhibitor; an ATP-competitive inhibitor of PDK1 and TBK1 (IC50s = 6 and 11 nM, respectively); an inhibitor of NUAK1 (IC50 = 5 nM), and MARK1, MARK2, MARK3, and MARK4 (IC50s = 55, 53, 81, and 19 nM, respectively), as well as MLK1, MLK2, and MLK3 (IC50s = 50, 46, and 42 nM, respectively); is selective for these kinases over five additional kinases (IC50s = >1,100 nM) but does inhibit VEGFR, as well as IΚΚε and Aurora B kinase (IC50s = 41 and 31 nM, respectively); inhibits phosphorylation of Akt at Thr308 and p70S6K1 at Thr389 in PC3 prostate cancer cells (IC50 = 300 nM); inhibits secretion of IFN-β induced by LPS or poly(I:C) in RAW 264.7 macrophages at 1 µM; inhibits the proliferation of PC3 and MDA-MB-468 cancer cells (IC50s = 250 and 720 nM, respectively); inhibits the proliferation of PDK1-/- murine embryonic stem cells expressing either wild-type PDK1 or PDK1 with an L159G mutation at 5 µM
保存温度:
-20
运输温度:
-20
预期分子量:
591.5
产品形式:
A crystalline solid
纯度:
≥98%
CAS号:
702675-74-9
分子式:
C23H26IN7O2S
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