CAS NO: | 2288709-96-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 |
AZ32 is an orally bioavailable and blood-brain barrier-penetratingATMinhibitor with anIC50of<6.2 nM forATMenzyme, and anIC50of 0.31 μM forATMin cell. |
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IC50& Target[1] |
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体外研究 (In Vitro) |
AZ32 is a next-generation blood-brain barrier (BBB)-penetrating ATM inhibitor. AZ32 blocks the DNA damage response and radiosensitized GBM cells in vitro[1].
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体内研究 (In Vivo) |
AZ32, with enhanced BBB penetration, is highly efficient in vivo as radiosensitizer in syngeneic and human, orthotopic mouse glioma model compared with AZ31. AZ32 is a specific inhibitor of the ATM kinase that possesses good BBB penetration in mouse. Following a single oral dose of AZ32 (200 mg/kg) in mice, the free-brain concentrations of AZ32 are in excess of the cellular IC50for approximately 22 hours[1].
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分子量 |
328.37 |
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性状 |
Solid |
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Formula |
C20H16N4O |
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CAS 号 |
2288709-96-4 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : ≥ 150 mg/mL(456.80 mM) *"≥" means soluble, but saturation unknown.
配制储备液
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In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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