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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1207293-36-4
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥920.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥350.0 |
| 规格: | 5 mg | 产品价格: | ¥900.0 |
| 规格: | 10 mg | 产品价格: | ¥1400.0 |
| 规格: | 25 mg | 产品价格: | ¥2800.0 |
| 规格: | 50 mg | 产品价格: | ¥4200.0 |
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BI-847325
CAS No. : 1207293-36-4
MCE 国际站:BI-847325
产品活性:BI-847325是MEK 和极光激酶 (AK)的ATP竞争性双重抑制剂, 对人类MEK2和AK-C的IC50值分别为4和15 nM。
研究领域:MAPK/ERK Pathway | Epigenetics | Cell Cycle/DNA Damage | Apoptosis
作用靶点:MEK | Aurora Kinase | Apoptosis
In Vitro: BI 847325 inhibits the activity of X. laevis AK-B with an IC50 of 3 nM; the IC50 values for human AK-A and AK-C are 25 and 15 nM, respectively. BI 847325 also inhibits human MEK1 and MEK2 with respective IC50 values of 25 and 4 nM. BI 847325 at 1,000 nM inhibits 6 enzymes by more than 50% (LCK, MAP3K8, FGFR1, AMPK, CAMK1D and TBK1) and the IC50 values are below 100 nM only for LCK (5 nM) and MAP3K8 (93 nM). Proliferation is inhibited in A375 and Calu-6 cell lines with GI50 values of 7.5 nM and 60 nM, respectively.
In Vivo: Daily oral administration of BI 847325 at 10 mg/kg shows efficacy in both BRAF- and KRAS-mutant xenograft models. BI 847325 administered once weekly at 70 mg/kg inhibits both MEK and AK in KRAS-mutant tumors.
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