SW044248
目录号: PL12358 纯度: ≥99%
CAS No. :522650-83-5
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中文名称
SW044248
中文别名
2-[(5-乙基-5H-1,2,4-三嗪并[5,6-B]吲哚-3-基)硫基]-N-(2-甲氧基苯基)丁酰胺;SW044248
英文名称
SW044248
英文别名
SW-044248;2-(5-ethyl-5H-[1,2,4]triazino[5,6-b]indol-3-ylthio)-N-(2-methoxyphenyl)butanamide;SW044248;2-((5-Ethyl-5H-[1,2,4]triazino[5,6-b]indol-3-yl)thio)-N-(2-methoxyphenyl)butanamide;2-[(5-ethyl-5H-[1,2,4]triazino[5,6-b]indol-3-yl)sulfanyl]-N-(2-methoxyphenyl)butanamide;Oprea1_566576;HMS1615G08;BCP16844;s6747;STK119518;ST094301;SW 044248;SW044248, >=98% (HPLC);2-(5-ethyl(1,2,4-triazino[5,6-b]indol-3-ylthio))-N-(2-m
Cas No.
522650-83-5
分子式
C22H23N5O2S
分子量
421.52
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
SW044248 是一种非典型的拓扑异构酶 I (topoisomerase I) 抑制剂,可以选择性地对某些非小细胞肺癌细胞产生毒性。
生物活性
SW044248 is a non-canonical topoisomerase I inhibitor, and selectively toxic for certain non-small cell lung cancer (NSCLC) cell lines.
性状
Solid
IC50 & Target[1][2]
Topoisomerase I
体外研究(In Vitro)
SW044248 is a non-canonical Top1 inhibitor, and is selectively toxic for certain NSCLC cell lines. SW044248 shows no effect on Top2. SW044248 (2, 5, 10 μM) rapidly inhibits transcription, translation and DNA synthesis in sensitive cells (HCC4017 and H292 cells) but not insensitive cells (HBEC30KT cells and HCC44 cells). SW044248 (10 μM) rapidly activates the integrated stress response through kinases GCN2 and PKR. The inhibition of Top1 in HCC4017 cells is helpful to the toxicity of SW044248. SW044248 (5, 10 μM) shows no effect on HBEC30KT and HCC44 cell lines due to the up-regulation of p21. SW044248 is selectively toxic in 18/74 NSCLC lines. 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]. Zubovych IO, et al. A Novel Inhibitor of Topoisomerase I Is Selectively Toxic for a Subset of Non-Small Cell Lung Cancer Cell Lines. Mol Cancer Ther. 2016 Jan;15(1):23-36.
[2]. Kim HS, et al. Systematic identification of molecular subtype-selective vulnerabilities in non-small-cell lung cancer. Cell. 2013 Oct 24;155(3):552-66.
溶解度数据
In Vitro: DMSO : 12.5 mg/mL (29.65 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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