168425-64-7
基本信息
2-嗎啉-4H-嘧啶并[2,1-A]異喹啉-4-酮
2-嗎啉基-4H-嘧啶并[2,1-A]異喹啉-4-酮
2-(嗎啉-4-基)嘧啶并[2,1-A]異喹啉-4-酮
2-嗎啉基-4H-嘧啶并[2,1-A]異喹啉-4-酮
2-MORPHOLINO-4H-PYRIMIDO[2,1-A]ISOQUINOLIN-4-ONE 2-嗎啉基-4H-嘧啶并[2,1-A]異喹啉-4-酮
Morpholino a
Compound 401, >=98%
COMPOUND401
COMPOUND-401
2-Morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one
2-(Morpholin-4-yl)pyrimido[2,1-a]isoquinolin-4-one
2-Morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one>
2-(4-Morpholinyl)-4H-pyrimido[2,1-a]isoquinolin-4-one
4H-PyriMido[2,1-a]isoquinolin-4-one, 2-(4-Morpholinyl)-
2-Morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one
物理化學(xué)性質(zhì)
報(bào)價(jià)日期 | 產(chǎn)品編號(hào) | 產(chǎn)品名稱 | CAS號(hào) | 包裝 | 價(jià)格 |
2024/11/08 | M2537 | 2-嗎啉基-4H-嘧啶并[2,1-a]異喹啉-4-酮 2-Morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one | 168425-64-7 | 10mg | 250元 |
2024/11/08 | M2537 | 2-嗎啉基-4H-嘧啶并[2,1-a]異喹啉-4-酮 2-Morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one | 168425-64-7 | 50mg | 955元 |
2024/11/08 | S6506 | COMPOUND 401 Compound 401 | 168425-64-7 | 5mg | 958.97元 |
常見(jiàn)問(wèn)題列表
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.