成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

返回ChemicalBook首頁(yè)>CAS數(shù)據(jù)庫(kù)列表>168425-64-7

168425-64-7

中文名稱 COMPOUND 401
英文名稱 COMPOUND 401
CAS 168425-64-7
分子式 C16H15N3O2
分子量 281.314
MOL 文件 168425-64-7.mol
更新日期 2023/03/20 15:41:19
168425-64-7 結(jié)構(gòu)式 168425-64-7 結(jié)構(gòu)式

基本信息

中文別名
化合物COMPOUND 401
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
英文別名
CS-315
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)

熔點(diǎn)184-186℃ (ethanol )
沸點(diǎn)456.9±55.0 °C(Predicted)
密度1.36±0.1 g/cm3 (20 ºC 760 Torr)
儲(chǔ)存條件Store at RT
溶解度DMSO : 6 mg/mL (21.33 mM; Need ultrasonic and warming)
酸度系數(shù)(pKa)1.01±0.20(Predicted)
形態(tài)粉末晶體
顏色白色至淺黃色
CAS 數(shù)據(jù)庫(kù)168425-64-7

安全數(shù)據(jù)

海關(guān)編碼2934.99.4400
COMPOUND 401價(jià)格(試劑級(jí))
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
2024/11/08M25372-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
168425-64-710mg250元
2024/11/08M25372-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
168425-64-750mg955元
2024/11/08S6506COMPOUND 401
Compound 401
168425-64-75mg958.97元

常見(jiàn)問(wèn)題列表

生物活性
Compound 401是DNA-PK和mTOR抑制劑(IC50分別為0.28 μM和5.3 μM)。它對(duì)p110α/p85α PI3K沒(méi)有明顯抑制作用,在COS7細(xì)胞中抑制S6激酶在Thr389位的磷酸化和Akt在Ser473位的磷酸化。
靶點(diǎn)
TargetValue
DNA-PK
(Cell-free assay)
0.28 μM
mTOR
(Cell-free assay)
5.3 μM
體外研究

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.

"168425-64-7" 相關(guān)產(chǎn)品信息