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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:
2226521-65-7
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1540.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥560.0 |
| 规格: | 5 mg | 产品价格: | ¥1400.0 |
| 规格: | 10 mg | 产品价格: | ¥2000.0 |
| 规格: | 25 mg | 产品价格: | ¥4100.0 |
| 规格: | 50 mg | 产品价格: | ¥6100.0 |
| 规格: | 100 mg | 产品价格: | ¥9500.0 |
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FM-381
CAS No. : 2226521-65-7
MCE 国际站:FM-381
产品活性:FM-381 是有效,共价,可逆的 JAK3 抑制剂,靶向 Cys909 位点。FM-381 对 JAK3 的 IC50 值为127 pM,选择性分别比 JAK1,JAK2 和 TYK2 高 410,2700 和 3600 倍。
研究领域:Epigenetics | Protein Tyrosine Kinase/RTK | JAK/STAT Signaling | Stem Cell/Wnt
作用靶点:JAK
In Vitro: FM-381 is screened against a panel of 410 kinases at concentrations of 100 nM and 500 nM. FM-381 has no relevant effect on the activity of any tested kinases except JAK3 at a concentration of 100 nM. At 500 nM, FM-381 moderately inhibits 11 other kinases besides JAK3 with residual activities below 50%. FM-381 is found to be inactive in a selectivity panel of frequently hit BRDs (BRD4, BRPF, CECR, FALZ, TAF1, BRD9). FM-381 selectively inhibits JAK3 signaling in human CD4+ T Cells. FM-381 shows an apparent EC50 of 100 nM in a dose dependent BRET assay and blocks IL2 stimulated (JAK3/JAK1 dependent) STAT5 phosphorylation at 100 nM, but not JAK3 independent IL6 (JAK1/2/TYK dependent) stimulated STAT3 signalling in human CD4+ T cells up to 1 µM.
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