L67 (Synonyms: DNA Ligase Inhibitor)
目录号: PL04469 纯度: ≥98%
CAS No. :325970-71-6
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中文名称
L67
中文别名
N-(3,5-二溴-4-甲基苯基)甘氨酸 [(2-羟基-5-硝基苯基)亚甲基]酰肼;Glycine, N-(3,5-dibroMo-4-Methylphenyl)-, 2-[(2-hydroxy-5-nitrophenyl)Methylene]hydrazide
英文名称
L67
英文别名
L67;DNA Ligase Inhibitor;L-67;N-(3,5-Dibromo-4-methylphenyl)-glycine 2-[(2-hydroxy-5-nitrophenyl)methylene]hydrazide;III inhibitor L67;LigI;LigI/III inhibitor L67
Cas No.
325970-71-6
分子式
C16H14N4O4Br2
分子量
486.12
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
L67 (DNA Ligase Inhibitor) 是一种竞争性的 DNA 连接酶抑制剂,能有效抑制 DNA 连接酶 I 和 III (IC50 都为 10 μM)。L67 (DNA Ligase Inhibitor) 可通过降低癌细胞线粒体 DNA 水平,增加线粒体活性氧水平,造成核 DNA 损伤。L67 (DNA Ligase Inhibitor) 还能激活癌细胞中依赖 Caspase 1 的凋亡通路,可用于癌症的研究。
生物活性
L67 (DNA Ligase Inhibitor) is a competitive DNA ligase inhibitor that effectively inhibits DNA ligases I/III (both IC 50 are 10 μM). L67 (DNA Ligase Inhibitor) can cause nuclear DNA damage by reducing levels of mitochondrial DNA and increasing levels of mitochondrially-generated ROS. L67 (DNA Ligase Inhibitor) also activates the Caspase 1-dependent apoptosis pathway in cancer cells, can be used in cancer research.
性状
Solid
体外研究(In Vitro)
L67 (10, 15 μM; 24 h) promotes nuclear DNA damage and (0-50 μM) increases level of mSOX by inhibiting mitochondrial LigIIIα in HeLa cells.
L67 (10 μM; 24 h) induces changes in mitochondrial function that causes a reduction in OCR and mitochondrial DNA, and abnormal mitochondrial morphology in HeLa.
L67 (10, 100 μM; 24 h) induces apoptosis in cancer cells.
L67 (0-30 μM; 24 h) selectively induces cell death in cancer cells by activating a caspase 1-dependent apoptotic pathway. has not independently confirmed the accuracy of these methods. They are for reference only.
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
参考文献
[1]. Sallmyr A, et al. Inhibiting Mitochondrial DNA Ligase IIIα Activates Caspase 1-Dependent Apoptosis in Cancer Cells. Cancer Res. 2016 Sep 15;76(18):5431-41.
[2]. Chen X, et al. Rational design of human DNA ligase inhibitors that target cellular DNA replication and repair. Cancer Res. 2008 May 1;68(9):3169-77.
溶解度数据
In Vitro: DMSO : ≥ 33 mg/mL (67.89 mM)H2O : 1 mg/mL (2.06 mM; Need ultrasonic)
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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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