化合物 T14569
中文名称 | 化合物 T14569 |
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中文同义词 | 化合物 T14569;N-[3-(氨甲基)苄基]-8-(4-苄基-1-哌嗪基)嘧啶并[5,4-D]嘧啶-4-胺 |
英文名称 | BI8626 |
英文同义词 | BI8626 (BI-8626;BI8626;1,3-Benzenedimethanamine, N1-[8-[4-(phenylmethyl)-1-piperazinyl]pyrimido[5,4-d]pyrimidin-4-yl]-;N-(3-(Aminomethyl)benzyl)-8-(4-benzylpiperazin-1-yl)pyrimido[5,4-d]pyrimidin-4-amine;N-[3-(Aminomethyl)benzyl]-8-(4-benzyl-1-piperazinyl)pyrimido[5,4-d]pyrimidin-4-amine |
CAS号 | 1875036-75-1 |
分子式 | C25H28N8 |
分子量 | 440.56 |
EINECS号 | |
相关类别 | |
Mol文件 | 1875036-75-1.mol |
结构式 | ![]() |
化合物 T14569 性质
沸点 | 654.4±55.0 °C(Predicted) |
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密度 | 1.302±0.06 g/cm3(Predicted) |
储存条件 | Store at -20°C |
溶解度 | DMSO:83.33 mg/mL(189.15 mM;需要超声波) |
形态 | 固体 |
酸度系数(pKa) | 9.01±0.10(Predicted) |
颜色 | 浅黄至黄色 |
IC50: 0.9 μM (HUWE1)
BI8626 induces HUWE1 ectopically expresses to abolishe ubiquitination of MCL1 in HeLa cells.
BI8626 suppresses colony formation of Ls174T cells with estimated IC
50
value of 0.7 μM, and BI8622 (1-4 days) treatment retards passage of Ls174T cells through all phases of the cell cycle, with the effect being strongest for G1.
BI8626 (0-50 μM; 0-6 hours) retards the degradation of MCL1 in response to UV irradiation to the same extent as depletion of HUWE1 in U2OS cells.
Cell Cycle Analysis
Cell Line: | Ls174T cells |
Concentration: | 0 μM, 5 μM,10 μM, 15 μM, 20 μM |
Incubation Time: | 0-4 days |
Result: | Retarded passage of Ls174T cells through all phases of the cell cycle, with the effect being strongest for G1. |
Western Blot Analysis
Cell Line: | U2OS cells |
Concentration: | 0 μM, 20 μM, 50 μM |
Incubation Time: | 0 hour,1 hour,2 hours,4 hours,6 hours |
Result: | Retarded the degradation of MCL1 in response to UV irradiation in HeLa cells by inhibiting HUWE1 in U2OS cells. |
安全信息
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
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2024/04/30 | HY-120204 | 化合物 T14569 BI8626 | 1875036-75-1 | 5mg | 2500元 |
2024/04/30 | HY-120204 | 化合物 T14569 BI8626 | 1875036-75-1 | 10mM * 1mLin DMSO | 2750元 |