COMPOUND 401
COMPOUND 401 性质
熔点 | 184-186℃ (ethanol ) |
---|---|
沸点 | 456.9±55.0 °C(Predicted) |
密度 | 1.36±0.1 g/cm3 (20 ºC 760 Torr) |
储存条件 | Store at RT |
溶解度 | DMSO:6 mg/mL(21.33 mM;需要超声波和加热) |
酸度系数(pKa) | 1.01±0.20(Predicted) |
形态 | 粉末晶体 |
颜色 | 白色至浅黄色至浅橙色 |
CAS 数据库 | 168425-64-7 |
COMPOUND 401 用途与合成方法
Target | Value |
DNA-PK
(Cell-free assay) | 0.28 μM |
mTOR
(Cell-free assay) | 5.3 μM |
Compound 401 is a potent inhibitor of DNA-PK (IC 50 =0.28 μM). Compound 401 is reported to be a poor inhibitor of PI3K, ATM, and ATR in vitro, but it is active against mTOR. Compound 401 shows activity against mTOR (IC 50 =5.3 μM) but not p110α/p85α PI3K (IC 50 >100 μM). Treatment of cells with Compound 401 blocks the phosphorylation of sites modified by mTOR-Raptor and mTOR-Rictor complexes (ribosomal protein S6 kinase 1 Thr 389 and Akt Ser 473 , respectively). By contrast, there is no direct inhibition of Akt Thr 308 phosphorylation, which is dependent on PI3K. Similar effects are also observed in cells that lack DNA-PK. Compound 401 inhibits immunoprecipitated epitope-tagged mTOR or endogenous mTOR in Raptor immunoprecipitates. In both cases, inhibition of 67% or 78% is obtained at 5 μM or 10 μM Compound 401, respectively. By contrast, dose response curves show that the p110α/p85α or p110β/p85α PI3K complexes are poorly inhibited by Compound 401 at these concentrations. The proliferation of TSC1 -/- fibroblasts is inhibited in the presence of Compound 401, but TSC1 +/+ cells are resistant.
COMPOUND 401 价格(试剂级)
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
---|---|---|---|---|---|
2024-11-08 | M2537 | 2-吗啉基-4H-嘧啶并[2,1-a]异喹啉-4-酮 | 168425-64-7 | 10mg | 250 |
2024-11-08 | M2537 | 2-吗啉基-4H-嘧啶并[2,1-a]异喹啉-4-酮 | 168425-64-7 | 50mg | 955 |