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目錄:MedChemExpress LLC>>生化試劑>> KU-60019 | MCE

KU-60019 | MCE
  • KU-60019 | MCE
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更新時(shí)間:2023-06-13 10:10:41瀏覽次數(shù):184評(píng)價(jià)

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CAS 925701-46-8 純度 99.43%
分子量 547.67 分子式 C??H??N?O?S
供貨周期 現(xiàn)貨 規(guī)格 5 mg
貨號(hào) HY-12061 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥
KU-60019 | MCEKU-60019 is an improved <b>ATM</b> kinase-specific inhibitor with <b>IC<sub>50</sub></b> of 6.3 nM.

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KU-60019

CAS No. : 925701-46-8

產(chǎn)品活性:KU-60019 is an improved ATM kinase-specific inhibitor with IC50 of 6.3 nM.

研究領(lǐng)域:Cell Cycle/DNA Damage  |  PI3K/Akt/mTOR

作用靶點(diǎn):ATM/ATR

In Vitro: KU-60019 is an improved analogue of KU-55933. KU-55933 has an IC50 of 13 nM and Ki of 2.2 nM in vitro and is highly specific for the ATM kinase using a panel of 60 protein kinases. KU-60019 is an improved inhibitor of the ATM kinase with an IC50 of 6.3 nM, approximately half that of KU-55933. The IC50 values for DNA-PKcs and ATR are 1.7 and >10 μM, respectively, almost 270-and 1600-fold higher than for ATM. KU-60019 is 10-fold more effective than KU-55933 at blocking radiation-induced phosphorylation of key ATM targets in human glioma cells. In human U87 glioma cells, KU-55933 completely inhibits phosphorylation of p53 (S15) at 10 μM but not at 3 μM, whereas γ-H2AX levels are only partly reduced with 10 μM 1 h after irradiation. By comparison, 3 μM KU-60019 completely inhibits p53 phosphorylation and partial inhibits at 1 μM.

In Vivo: Despite PTEN-deficient control tumors reaching a 4-fold increase in size before PTEN wild-type controls, KU-60019-treated PTEN-deficient tumors display a statistically significant slowing in growth. This growth inhibition is especially evident at the start of the experiment (days 5-12) just after KU-60019 is administered (days 1-5).

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