| CAS: | 883046-50-2 | ||||
| 分子式: | C17H14FNO4 | ||||
| 分子量: | 315.3 | ||||
| 英文名称: |
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| 用途: | S14161 is a small molecule inhibitor of cyclins D1-D3 expression that inhibits phosphoinositide 3-kinase activity and arrests cells at the G0/G1 phase in a dose-dependent manner |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||||||||||||||
| S911584 | MACKLIN | S14161 | 98% | 771元/1mg; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||
储存:-20°C,密闭,干燥 | |||||||||||||||||||||||||||||||||||||||||||||||
| SML1571 | Sigma-Aldrich | S14161 | ≥98% (HPLC) | 833.87元/1 MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||
产品说明 包装 1, 5 mg in glass bottle 生化/生理作用 S14161 inhibits D-cyclin transactivation by inhibition of phosphoinositide 3-kinase (PI3K) activity. S14161 is a pan-class I PI3K inhibitor. S14161 inhibited the activity of all 4 isoforms of the PI3K class I family, and unlike LY294002, had little effect on class IV enzymes mechanistic target of rapamycin (mTOR) and DNA-PKcs (DNA-dependent protein kinase, catalytic subunit), or on AKT-1, -2, or -3 or PDK1. S14161 inhibited the expression of cyclins D1, D2, and D3, leading to the arrest of cells at the G0/G1 phase, and has exhibited anti-myeloma and anti-leukemia activity with no gross toxicity. 基本信息
产品性质
安全信息
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