AZD-7648
目录号: PL09824 纯度: ≥99%
CAS No. :2230820-11-6
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中文名称
AZD-7648
英文名称
AZD-7648
英文别名
AZD7648;AZD-7648;97A09L5JCK;7-methyl-2-((7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)amino)-9-(tetrahydro-2H-pyran-4-yl)-7,9-dihydro-8H-purin-8-one;7-Methyl-2-((7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)amino)-9-(tetrahydro-2H-pyran-4-yl)-7H-purin-8(9H)-one;7-methyl-2-[(7-methyl-[1,2,4]triazolo[1,5-a]pyridin-6-yl)amino]-9-(oxan-4-yl)purin-8-one;GTPL10601;US10407446, Example 3;BDBM413450;BCP30676;AZD 7648;AZD7648;N
Cas No.
2230820-11-6
分子式
C18H20N8O2
分子量
380.40
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
AZD-7648 是一种具有选择性的口服有效 DNA-PK 抑制剂,IC50 值为 0.6 nM, AZD-7648 诱导细胞凋亡 (apoptosis),具有抗肿瘤活性。
生物活性
AZD-7648 is a potent, orally active, selective DNA-PK inhibitor with an IC 50 of 0.6 nM. AZD-7648 induces apoptosis and shows antitumor activity.
性状
Solid
IC50 & Target[1][2]
DNA-PKcs 91.3 nM (IC50) PI3Kγ 1.37 μM (IC
体外研究(In Vitro)
AZD7648 (0-30 μM) is a potent radiosensitizer.
AZD7648 (3 μM) increases sensitivity to doxorubicin.
AZD7648 (0.6 μM) enhances the activity of PARP inhibitor olaparib. has not independently confirmed the accuracy of these methods. They are for reference only.Western Blot Analysis
体内研究(In Vivo)
AZD-7648 (100 mg/kg; p.o.; once daily for 5 days) induces tumour growth inhibition and tumour regression. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Nude mice, A549 xenografts an
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Fok JHL, et al. AZD7648 is a potent and selective DNA-PK inhibitor that enhances radiation, chemotherapy and olaparib activity. Nat Commun. 2019 Nov 7;10(1):5065.
溶解度数据
In Vitro: DMSO : 5 mg/mL (13.14 mM; ultrasonic and warming and heat to 80°C)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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