PARP1-IN-8
目录号: PL08879 纯度: ≥99%
CAS No. :836640-15-4
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中文名称
PARP1-IN-8
英文名称
PARP1-IN-8
英文别名
N-(3-chlorophenyl)-3-(1-oxo-4-phenylphthalazin-2(1H)-yl)propanamide;2(1H)-Phthalazinepropanamide, N-(3-chlorophenyl)-1-oxo-4-phenyl-;PARP1-IN-8
Cas No.
836640-15-4
分子式
C23H18ClN3O2
分子量
403.86
包装储存
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
产品详情
PARP1-IN-8 (化合物 11c) 是一种有效的可透过血脑屏障的 PARP1 抑制剂,其 IC50 值为 97 nM。PARP1-IN-8 对人肺腺癌上皮细胞系 A549 具有显著的抗增殖活性。
生物活性
PARP1-IN-8 (compound 11c) is a potent and BBB-penetrated PARP1 inhibitor, with an IC 50 of 97 nM. PARP1-IN-8 shows significantly potent anti-proliferative activity against Human lung adenocarcinoma epithelial cell line A549.
性状
Solid
IC50 & Target[1][2]
PARP-1 97 nM (IC50)
体外研究(In Vitro)
PARP1-IN-8 (compound 11c) (0-10 μM, 24-48 h) shows significantly potent anti-proliferative activity against A549 cells. has not independently confirmed the accuracy of these methods. They are for reference only.Cell Proliferation Assay
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. Almahli H, Hadchity E, Jaballah MY, Daher R, Ghabbour HA, Kabil MM, Al-Shakliah NS, Eldehna WM. Development of novel synthesized phthalazinone-based PARP-1 inhibitors with apoptosis inducing mechanism in lung cancer. Bioorg Chem. 2018 Apr;77:443-456.
溶解度数据
In Vitro: DMSO : 62.5 mg/mL (154.76 mM; Need ultrasonic)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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